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  • Articles  (1,258)
  • Springer  (1,258)
  • Nature Publishing Group
  • 1990-1994
  • 1980-1984  (1,258)
  • 1981  (1,258)
  • Process Engineering, Biotechnology, Nutrition Technology  (1,258)
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  • Articles  (1,258)
Publisher
Years
  • 1990-1994
  • 1980-1984  (1,258)
Year
Journal
  • 1
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    Applied microbiology and biotechnology 13 (1981), S. 161-164 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A strain ofFusarium moniliforme, previously used for microbial protein production, excreted lactase (β-D-galactosidase, EC.3.2.1 23) when cultivated either in a whey liquid medium or on a wheat bran solid medium. The enzyme produced in both media had pH and temperature optima of 4–5 and 50–60°C respectively and was particularly suitable for processing acid whey. In the whey culture, maximum lactase yield was observed after 95 h of growth at 30°C and whey lactose concentration of 9%. The addition of ammonium, potassium and sodium ions to the growth medium considerably enhanced lactase production. A maximum enzyme yield corresponding to hydrolysis of 3 nmoles o-nitrophenyl-β-D-galactopyranoside sec−1 ml−1 of growth medium, at pH 5 and 60°C, was obtained. In the wheat bran culture, the maximum enzyme yield was obtained after 140 h of growth at 28–30°C. A marked increase in the enzyme production was observed when nitrate or phosphate was added to the growth medium. Also, the addition of certain agricultural by-products (molasses, whey) enhanced lactase production. The observed maximum yield corresponding to the hydrolysis of 182 nmoles of ONPG sec−1 g−1 of wheat bran, at pH 5 and 60°C, is comparable to that reported for certain microorganisms used commercially for lactase production.
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  • 2
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    Applied microbiology and biotechnology 13 (1981), S. 175-178 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Biological treatment of waste water containing a large amount of phenol was carried out by using a phenolassimilating fungus,Aureobasidium pullulans No. 14 adhered (“semi-immobilized”) to fibrous asbestos. The column reactor employed for oxidative degradation of phenol consisted of a cylindrical glass column containing plastic nets. During 27 days operation, it was observed that: 1) The phenol removal capacity of the reactor gradually increased during the first 10 days, reaching a stable level. 2) The best phenol removal capacity (50 mg phenol removed/h/ liter of reactor volume) was obtained when an artificial waste water containing up to 1,200 μg/ml phenol was applied to the reactor. 3) Much higher concentrations of phenol (e.g. 1,700 μg/ml) brought about a marked decrease in the phenol removal capacity (40–50 mg/h/liter). 4) Satisfactorily stable operation was achieved using the semiimmobilized mycelia ofAureobasidium pullulans, whose active state could be checked by observing the thick, black-colored biomass which is characteristic of the genusAureobasidium and covered the plastic nets inside the glass column reactor.
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  • 3
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    Applied microbiology and biotechnology 13 (1981), S. 188-190 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The alkane oxidation byChlorella vulgaris is improved by disruption of the cells. Although living cells are not able to attack n-dodecane, disrupted cells produced detectable amounts of oxidation products. The amount of isomeric alcohols and ketones of n-tridecane was nearly double the sum found in living cells, whereas the equilibrium was shifted to the ketones. With n-tetradecane and n-pentadecane only the amount of ketones increased.
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  • 4
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    Applied microbiology and biotechnology 13 (1981), S. 213-215 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Purification of the Bacillus thuringiensis protein crystal on NaBr density gradients confers a significant technical advantage in that the crystal-associated proteases are thereby removed. The use of protease-free crystals allows reliable determination of native crystal parameters.
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  • 5
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    Applied microbiology and biotechnology 13 (1981), S. 226-231 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Carboxymethyl-cellulase and β-glucosidase activities were determined in the cytosole, cell walls and extracellular culture fluid of Trichoderma reesei QM 9414 cultivated on cellulose and cellobiose. By means of carboxymethylcellulose as a specific desorbens for cellulose bound CM-cellulase and β-glucosidase it was found that these enzymes are cell wall bound during consumption of the carbon source, but are excreted during the subsequent cultivation stage. Treatment of intact cell walls with various chemical agents could not cause a release of the enzyme. Treatment of intact cell walls with α-mannanase or trypsin released CM-cellulase, whereas, treatment with laminarinase or chitinase released β-glucosidase. Both enzymes were also released during autolysis in phosphate buffer. This autolysis was accompanined by the appearance of extracellular mannanase, laminarinase and proteinase. The results suggest that cleavage of chemical bonds of certain cell wall polymers of T. reesei could be responsible for the appearance of CM-cellulase and β-glucosidase in the culture fluid during later stages of growth.
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  • 6
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    Applied microbiology and biotechnology 13 (1981), S. 248-250 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Wheat was ensiled and periodically analyzed for lactic acid bacteria present. Initially Lactobacillus plantarum, Leuconostoc mesenteroides, Lactobacillus cellobiosus and Streptococcus lactis predominated. After two to four days enterococci including S. faecium and S. bovis were present in high populations as well as Lactobacillus plantarum. It was concluded that mixed populations of enterococci and L. plantarum are active in the successful fermentation of wheat silage.
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  • 7
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    Applied microbiology and biotechnology 13 (1981), S. 251-253 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Conclusions The use of polarized U.F. membrane enzymatic reactors yields considerable stabilization of the enzyme activity because of the high concentration levels attained by the protein in the polarization layer. Further enzyme stabilization is achieved when even higher overall concentrations are attained by injecting an inert, linear-chain polymer into the system. Both effects are a direct consequence of the polarization phenomena that take place in an unstirred system and hence disappear when dealing with a stirred cell. No appreciable reduction in initial enzyme activity level occurs in the polarized system as compared to the soluble enzyme situation.
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  • 8
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    Applied microbiology and biotechnology 11 (1981), S. 97-105 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Hansenula polymorpha was cultured for long periods in 254 cm high single and three-stage countercurrent tower loop reactors 20 cm in diameter using ethanol as a substrate in the absence and presence of antifoam agents (Desmophen 3600 and/or soy oil). In the absence of antifoam agents in the three-stage column, much higher volumetric mass transfer coefficients were attained than in the corresponding single-stage column. The cell productivity in the former, however, was only slightly higher than in the single-stage column due to considerable enrichment of the cells in the foam and nonuniform cell concentration distribution in the three-stage column. In the presence of antifoam agents the three-stage column has a higher cell productivity, OTR, kL a and a lower specific energy requirement with regard to the absorbed oxygen and/or produced cell mass than the single stage column. The reactor performance is especially high if the bubbling layer height is reduced to 20 cm. Soy oil has considerably less foam eliminating property than Desmophen. Since the soy oil is metabolized by the yeast, large amounts are needed to operate these reactors.
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  • 9
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    Applied microbiology and biotechnology 11 (1981), S. 110-115 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Surface rheological properties of CMC (carboxymethyl cellulose), PAA (polyacrylamide) and BSA (bovine serum albumin) solutions were determined by the method of Hansen and Lucassen in which the variation in damping coefficient is measured with regard to distance of capillary waves produced by a vibrating probe on a liquid surface. The surfaces of these solutions have highly viscoelastic properties at concentrations at which the bulk viscosities are already Newtonian.
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  • 10
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    Applied microbiology and biotechnology 11 (1981), S. 116-119 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Changes in the nutritional media significantly affected specific glucose uptake rate (Qg), glucose utilization and ethanol production rate (Qp) of Zymomonas mobilis Z 10. Varying the yeast extract concentrations (pantothenate) between 0.15% and 1.0% in a 10% glucose system at μ=0.2 h−1, Qg values between 14.9 and 35.3 and Qp values between 7.4 and 14.6 were obtained. A concentration of 0.25% yeast extract gave highest results. High NH 4 + concentrations were detrimental to ethanol production, whereas phosphate, potassium and magnesium stimulated the catabolic activity. In the case of magnesium, glucose utilization increased from 2.8 to 92.2%. Batch and continuous cultures showed that by increasing catabolic activity, ethanol productivity can be increased irrespective of glucose concentration.
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  • 11
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The effect of ethanol on yeast growth and fermentation has been studied in two strains, NCYC479 (a commercial saké yeast) and 5D-cyc (a laboratory haploid strain). The effect of ethanol on growth was similar in the two strains. It showed complex kinetics which resulted from both the inhibition of the growth rate itself and also a reduction in cell viability. The growth and viability effects had different inhibition constants. Ethanol was less inhibitory toward fermentation than toward growth. Fermentation in the saké yeast was more ethanol tolerant than in the laboratory strain. The inhibition kinetics for fermentation were less complex than those for growth and followed the classical noncompetitive pattern.
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  • 12
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    Applied microbiology and biotechnology 11 (1981), S. 156-160 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary As the hydrolysis of mandarin orange peel with macerating enzyme (40°C, 24 h) produced 0.59 g g−1 reducing sugar per dry peel compared to 0.36 by acid-hydrolysis (15 min at 120°C with 0.8 N H2SO4), the production of single cell protein (SCP) from orange peel was studied mostly using enzymatically hydrolyzed orange peel. When the enzymatically hydrolyzed peel media were used, the utilization efficiency of reducing sugars (%) and the growth yield from reducing sugars (g g−1) were: 63 and 0.51 for Saccharomyces cerevisiae; 56 and 0.48 for Candida utilis; 74 and 0.69 for Debaryomyces hansenii and 64 and 0.70 for Rhodotorula glutinis. SCP production from orange peel by D. hansenii and R. glutinis were further studied. Batch cultures for 24 h at 30°C using 100 g dried orange peel produced 45 g of dried cultivated peel (protein content, 33%) with D. hansenii and 34 g (protein content, 50%) with R. glutinis, and 38 g (protein content, 44%) with a mixture of both yeasts.
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  • 13
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    Applied microbiology and biotechnology 11 (1981), S. 161-165 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Out of 17 strains of 14 different Bacillus species, Bacillus cereus ATCC 7064 produced the highest levels of p-nitrophenyl-α-D-glucopyranoside-hydrolyzing α-glucosidase. Maximal enzyme yield was achieved after 6 h of cultivation, at an initial pH of 6.5–7.0, on a medium containing 2% soluble starch, 2% peptone, 0.3% yeast extract, 0.05% meat extract, 0.3% K2HPO4 and 0.1% KH2PO4. When grown on 2% starch, B. cereus synthesized α-glucosidase in the cytoplasm. At a starch concentration of less than 1%, however, the enzyme appeared in the culture broth. This accumulation was maximal at 0.4% starch when the extracellular enzyme amounted to 54% of the total enzyme produced.
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  • 14
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    Applied microbiology and biotechnology 11 (1981), S. 166-171 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A procedure for purification of a serine alkaline proteinase from Streptomyces rimosus waste broth was developed. The procedure includes ultrafiltration, CM-Sephadex C-50 and CM-cellulose chromatography and gel filtration on Sephadex G-75. The recovery of electrophoretically pure enzyme was 25%. The enzyme is active on different protein and synthetic substrates at neutral and alkaline pHs but its activity on hemoglobin and bovine serum albumin, is optimal at pH 4.0–4.5. It has a molecular weight of 22,000 and a pI of 4.90. The enzyme is inhibited by DFP and PMSF but not by TPCK. Its substrate specificity, amino acid composition and some other properties were also determined.
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  • 15
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    Applied microbiology and biotechnology 11 (1981), S. 172-178 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Heat treatment (10 min at 65° C) of cells of Alcaligenes eutrophus, which resulted in the release of RNA degradadation products into the medium, was found to activate cellular ribonucleases. Two ribonucleases degrading yeast RNA were found, one localized in the periplasmic space and the other in the soluble fraction of the ribosomes. Compared to non-heated cells, in the heat-treated cells the former enzyme, the cell debris ribonuclease, was present at an eightfold increased specific activity, and the latter, the cytoplasmic ribonuclease, was present at a fourfold increased specific activity. This increase was due to the inactivation of a thermolabile inhibitor and to denaturation of part of the soluble protein during heat treatment. With respect to their properties the enzymes were similar; they had endonuclease activity and hydrolysed only RNA. They were heat-stable, resistent to trypsin, highly sensitive to a ribonuclease inhibitor isolated from the same bacterium and were partially inhibited by ATP and GTP. These properties provided a partial explanation for the mechanism of the release of RNA dagradation products from A. eutrophus cells after heat treatment.
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  • 16
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    Applied microbiology and biotechnology 11 (1981), S. 179-182 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Growth of Tetrahymena pyriformis (Gl) was studied in axenic culture in the presence of cadmium. The maximum growth rate is not affected by concentrations of cadmium below 1.5 mg/l (1.3×10−5 M). The concentration reducing the growth rate to 50% of its initial value is 2.6 mg/l (2.3×10−5 M) and the lethal dose is 5 mg/l (4.5×10−5 M). The mean cell volume, mean cell dry weight, mean cell protein content, yield and respiration rate were compared at 0, 0.2 and 2.0 mg/l Cd. No significant differences were detected for these parameters between control and treated groups.
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  • 17
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    Applied microbiology and biotechnology 11 (1981), S. 189-192 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The sensitivity of the radiometric detection of microbial contamination based on the labeling of cells by 14C-lysine was studied as a function of the lysineconcentration and its specific activity for a strain of E. coli and a strain of S. cerevisiae. It was found that best conditions of detection were given by a labelled lysine specific activity of 200 mCi/mmole and a medium radioactivity of 0.2 μCi/ml.
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  • 18
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    Applied microbiology and biotechnology 13 (1981), S. 165-169 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary It is demonstrated for the first time that a species from the genusHumicola is a potential source of acid protease. A strain was classified by morphological investigations asHumicola lutea. The influence of constituents of the culture medium on the growth and acid protease production ofH. lutea 72 in submerged cultivation in flasks was investigated. An improved medium was devised for future studies. The optimal aeration rate, inoculum level and cultivation time were determined. A maximal proteolytic activity of 670 μg tyrosine liberated from casein ml−1 culture filtrate min−1 at pH 3.0 was obtained.
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  • 19
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    Applied microbiology and biotechnology 13 (1981), S. 179-183 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Analysis of the enzymes involved in the biosynthesis of alginic acid by mucoidPseudomonas aeruginosa PAO strain's determined the presence of enzymes required to synthesise GDP-mannuronic acid. Addition of polymannuronic acid to an ammonium sulphate precipitate of a cell free alginate suspension indicated the presence of an enzyme which catalysed the epimerisation of mannuronic acid to guluronic acidafter the polymer had been synthesised. The epimerase was shown to be calcium dependant. Various non-mucoid mutants were also studied. The non-mucoid parental strain PAO 381 also contained the enzymes required for alginate synthesis but they were not expressed. Synthesis of alginic acid led to an increase in the level of these enzymes. In the non-mucoid mutants derived from mucoid parents GDP-mannose dehydrogenase was absent in all strains studied. In some of these strains GDP-mannose pyrophosphorylase was also absent, while in other strains, phosphomannase isomerase was absent or greatly reduced.
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  • 20
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary In order to obtain a better understanding of the behaviour ofPediococcus pentosaceus in food products as well to facilitate the designing of industrial production processes for the organism, the growth and lactic acid production ofPediococcus pentosaceus in a complex glucose medium was followed in batch cultures at different gas environments (CO2, air, N2 and static cultures without gasflow), temperatures (10–50°C), pH (4.3–7.3) and nitrite concentrations (0–700 ppm). Optimal growth was obtained in CO2 at 40°C and pH 6.3 and resulted in a maximum specific growth rate (μ max) of 1.27 h−1. In static culture at 40°C and pH 6.3 theμ max was 1.21 h−1. Theμ max was, compared with static culture, reduced in air (12%) and nitrogen (26%). At 10°C theμ max was reduced by 99% and at 50°C by 88%. The reduction at pH 4.3 and 7.3 was 65% and 57%, respectively. Nitrite did not affect theμ max at any pH but increased the lag phase at pH 4.3 by a factor of 12. The lactic acid production was linked to the growth. The total amount of lactic acid produced was the same in all the tested gases and nitrite concentrations and also within the wide temperature range (15–45°C) and pH range (5.3–7.3). Mainly L(+)-lactic acid was produced during the exponential growth phase, but after this growth declined about 30% of the L(+)-lactic acid was converted to D(−)-lactic acid. The lactic acid product yield and the cellmass yied were both affected by the temperature but not by the pH.
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  • 21
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    Applied microbiology and biotechnology 13 (1981), S. 191-193 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
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  • 22
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    Applied microbiology and biotechnology 13 (1981), S. 194-195 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
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  • 23
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    Applied microbiology and biotechnology 13 (1981), S. 208-212 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A filamentous fungus Penicillium cyclopium, capable of growing on deproteinized whey was isolated and characterized for the purpose of production of microbial protein. This organism has a maximum specific growth rate of 0.2 h−1 at pH 3.0 to 4.5 and 28°C in a medium containing only ammonium nitrogen and deproteinized whey. The yield coefficients are 0.68 g biomass/g lactose, 12.0 g biomass/g nitrogen, and 2.10 g biomass/g oxygen, respectively. Crude protein and total nucleic acid contents of this organism are 47.5% and 7.4% (dry cell weight basis), respectively. The profile of essential amino acids shows that it could be a good source of animal feed or food protein.
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  • 24
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    Applied microbiology and biotechnology 13 (1981), S. 216-221 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A new rapid-plate test for the detection of arylsulfatase activity was developed for the screening of exo-arylsulfatase-bearing micro-organisms. A method for the detection of free sulfate groups, based on atomic absorption spectrophotometry, was modified for the purpose of measuring sulfate released from lignosulfonate. The effect of lignosulfonate on arylsulfatase activity from various sources was studied. The sulfate requirements of two isolates were studied. Two isolates were found to release over 60% of the sulfate ester present in the lignosulfonate during growth. Desulfonation activity was demonstrated for the first time in a cell free extract of micro-organisms; two extracts released all the detectable sulfate ester from the lignosulfonate and two others apparenty released all the sulfate ester groups from the lignosulfonate and some of the sulfonic groups.
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  • 25
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    Applied microbiology and biotechnology 13 (1981), S. 232-235 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The inhibitory effect of roquefortine, a secondary metabolite of Penicillium roqueforti, on bacterial protein, RNA and DNA synthesis was studied. Similar results were obtained in colorimetric measurements and in studying the incorporation of radioactive precursors. They show that RNA synthesis was most significantly affected by roquefortine. Inhibition of protein and DNA synthesis was less pronounced and might be a result of primary inhibition of RNA synthesis.
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  • 26
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    Applied microbiology and biotechnology 13 (1981), S. 242-247 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The rates of glucose utilization by fermentative bacteria and propionate and butyrate utilization by acetogenic bacteria were studied and their dependence of pCO2 in the interval 0–1 bar was determined. A batch fermentation method was used permitting good control of fermentation parameters and rapid experiments. The rate of glucose fermentation to acids, CO2 and H2 was in the order of 12,000 mg glucose/l · day which was about two orders of magnitude faster than the utilization of propionic and butyric acid by acetogenic bacteria. The rate of glucose utilization was about 30% greater at low values of pCO2 compared with 1 bar CO2. Propionate degradation was strongly affected by pCO2; rates were 60 mg/l · day at pCO2=1 bar and 200 mg/l · day at pCO2=0.2 bar. Some CO2 was required since the rate of propionate utilization dropped rapidly below pCO2=0.2 bar. The rate of butyric acid utilization was constant at 170 mg/l · day; slightly lower at pCO2=1 bar. Yields of methane from glucose or acids were close to the theoretical value 50% of degraded substrate-carbon. Yields were 20–30% higher at low values of pCO2 compared with 1 bar CO2. The redox potential was usually between −200 and −250 mV, slowly increasing to between −150 and −200 mV during fermentation. No clear connection between rates of substrate utilization, pCO2 and Eh was detected.
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  • 27
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Immobilized dried yeast cells, which contain glycolytic and some other emzymes, required NAD but not ATP for the (e.g. choline kinase, pyrophosphorylase) fermentative production of CDP-choline, when washed and reused. The immobilized system was more resistant to heat than dried cells, which had previously been used for the same purpose. However, when too many cells were immobilized, leakage of the enzymes from the resin lattice was observed during repeated use. To prevent this leakage, the ratio of cells to resin should be considered.
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  • 28
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    Applied microbiology and biotechnology 11 (1981), S. 106-109 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A simple method was developed for evaluating foam stability. The influence of KCl and MgSO4 on foam stability of bovine serum albumin foams was investigated. These salts increase foaminess, but diminish foam stability by the same degree. Thus there is little overall.
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  • 29
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    Applied microbiology and biotechnology 11 (1981), S. 81-88 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Maximization of microbial two-step conversion of 9α-fluorohydrocortisone to Δ1-dehydro-16α-hydroxy-9α-fluorohydrocortisone (triamcinolone) in a mixed culture of two microorganisms, Arthrobacter simplex and Streptomyces roseochromogenus, was attempted by a digital simulation, to optimize an operational parameter, pH, during batch cultivation. A mathematical model of the steroid transformation in the mixed culture was constructed with nine differential equations. The kinetic parameters other than the Michaelis-Menten constants in the mathematical model varied with pH of the culture medium. The mathematical model facilitated the simulation of the effect of pH on steroid conversion in the mixed culture. A modified Simplex method of direct search was applied to optimize the switching time and the combination of pH values in the batch culture with several step-changes of pH. Varied-pH processes showed much higher conversion yields than the constant pH process. A process of 3-phase pH change is expected to be advantageous in practical operation because of its lower susceptibility to pH perturbation, though the yield is almost the same as that of the 2-phase process.
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    Applied microbiology and biotechnology 11 (1981), S. 89-96 
    ISSN: 1432-0614
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    Notes: Summary Hansenula polymorpha was cultured for extended periods in an air lift tower loop reactor (15 cm in diameter with a 275 cm bubbling layer height) with ethanol and/or glucose as the substrates. At constant operation conditions variations of the following parameters were measured: the consumption of the substrate and oxygen, the production of CO2 and biomass, the longitudinal concentration profile of dissolved oxygen, the oxygen and substrate yield coefficients, the respiratory quotient and the specific interfacial area and volumetric mass transfer coefficient. The influence of the microorganisms on the oxygen transfer rate is discussed especially in the case of glucose repression.
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    Applied microbiology and biotechnology 11 (1981), S. 120-124 
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    Notes: Summary Of fungi 110 strains were screened for extracellular cellulase production in shake flask experiments. Twelve strains produced the enzyme in significant quantity. Since the enzyme activity was assayed by different methods (liberation of reducing sugar from cotton, filter paper, carboxymethylcellulose and cellobiose), the estimation of the productivity of the strains differed according to the substrate used. The best cotton degrading activity per fermentation volume as well as per mg of secreted soluble protein was achieved by Penicillium verruculosum WA 30, a wild-type strain, for which the cellulase productivity has not yet been published. The cotton degrading (so-called C1) activity was successfully enhanced nearly threefold in medium experiments. Analyses of saccharification digests showed that glucose was the predominant product, with negligible amounts of cellobiose. The pH and temperature optima for WA 30 cellulase complex were pH 4.2 and 60°C.
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    Applied microbiology and biotechnology 11 (1981), S. 131-132 
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    Applied microbiology and biotechnology 11 (1981), S. 125-130 
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    Notes: Summary This study determined how processing in cook/chill foodservice systems affected the quantity of sublethally injured bacteria in food. Beef loaf and frozen green beans were each prepared three times in a laboratory simulation following time-temperature recommendations of the Hazard Analysis Critical Control Point model. Beef loaf (15 kg) was initially cooked (1 kg/loaf) to a mean and temperature of 66°C; stored 24 h at 6°C and sliced, 100 g/poriton. Beans (4.5 kg) were removed from the freezer, stored 24 h at 6°C, and portioned, 100 g/ portion. Portions were helds at 6°C for 2 h and then were microwave-heated individually for 20, 50, 80, or 110s. Samples were then plated using Plate Count Agar (PCA) to obtain aerobic plate count (APC) and PAC plus 3.0% (beans) or 4.5% (beaf loaf) sodium chloride. The difference in results between the two counts (APC less PCA + NaCl) was defined as a measure of sublethally injured bacteria in the sample. The proportion of injured cells in beef loaf before microwave-heating was larger than that in green beans before microwave-heating probably because the beef loaf was initially cooked. Lenghtening the time of microwave-heating increased the proportion of injured cells in all microwave treatments of beef loaf and also in green beans when the time was 50 or more seconds.
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    Applied microbiology and biotechnology 11 (1981), S. 133-138 
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    Notes: Summary Bacterial chromatophores have been isolated from a purple non-sulfur bacterium (Rhodopseudomonas capsulata) by sonication and immobilized within various supports. In each case, the activity yield after immobilization and the storage stability (under dark conditions at 4°C) have been determined. Some preliminary comparative experiments concerning the ATP production in a batch reactor are presented for native and immobilized chromatophores.
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    Applied microbiology and biotechnology 11 (1981), S. 139-145 
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    Notes: Summary In submerged culture there was negligible growth of Fusarium moniliforme with either n-tetradecane or gasoil (C13−C19) as the only carbon and energy source. In surface culture the cell yield was about 0.25 g dm−3 dry weight after four weeks incubation. Some oxidation products, mainly isomeric tetradecanones (4-one, 5-one, 6-one and 7-one), could be identified. However the cell yield in a trickle-flow column was about 3 g dm−3 dry weight after 7 days. Only traces of oxidation products could be detected. In a fixed-bed reactor, filled with glass rings, cell yields were similar to those in the trickle-flow column and depended on the medium flow rate. After termination of growth in the fixed-bed reactor, similar amounts of gibberellic acid were produced in a nitrogen-free medium with either gasoil or glucose.
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    Notes: Summary dl-Menthyl succinate was successfully hydrolyzed stereoselectively by Rhodotorula minuta var. texensis cells entrapped within photo-crosslinked or polyurethane resin gels in water-saturated n-heptane. The hydrolyzed product was found to be pure l-menthol. The catalytic activity of the immobilized cells, especially those entrapped in urethane polymers, was far more stable than that of the free cells. The half-life of the polyurethaneentrapped cells was estimated to be 55–63 days in the organic solvent.
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    Applied microbiology and biotechnology 11 (1981), S. 183-188 
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    Notes: Summary In laboratory and semi-industrial scale experiments the influence of the substrate water content, temperature, and incubation time on the progress of solid state fermentation of straw colonized by white rot fungi was investigated. The parameters used to evaluate the fermentation process were degradation of total organic matter and lignin, in vitro digestibility, the content of water soluble substances in the substrate and the pH. The degradation of total organic matter was species specific. Only Trametes hirsuta enhanced the degradation at elevated temperature (30 °C). With Abortiporus biennis, Ganoderma applanatum, and Pleurotus serotinus, elevated temperature had and adverse effect. Prolonged incubation only improved degradation of straw by the relatively slowgrowing fungi Ganoderma applanatum, Lenzites betulina, and Pleurotus sajor caju. Elevated temperature and prolonged incubation shifted the relative degradation rates in favour of total organic matter degradation. With Ganoderma applanatum, Pleurotus ostreatus, and Pleurotus serotinus lignin degradation, even on an absolute scale, was less at 30 °C than at 22 °C. In general, the in vitro digestibility also decreased, when the incubation time and temperature were raised. With Ganoderma applanatum the in vitro digestibility dropped below the value of the sterile straw control. Solid state fermentation of straw was at an optimum at a medium water content of 75 ml/25 g of substrate. However, most of the fungi tested could digest straw over a wide range of water content. At higher water contents (125–150 ml/25 g of substrate) an increased production of aerial mycelium was observed. In semi-industrial batch experiments (40 kg) with Abortiporus biennis the in vitro digestibility dropped below the reference value for sterile straw during the first 19 days of incubation. Later, the in vitro digestibility again rose and reached its optimum after about 60 days. The in vitro digestibility in the semi-industrial experiments was always lower than in the laboratory experiments (+9% and +25%, respectively). In long term experiments (2.5 kg batches, 8 months of incubation) very different values for the in vitro digestibility were found, and these depended on the fungus used (Abortiporus biennis, +16%; Pleurotus ostreatus, +4%; and Ganoderma applanatum, −27%).
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    Applied microbiology and biotechnology 11 (1981), S. 205-211 
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    Notes: Summary The growth of yeast cells on glucose in chemostat cultures at dilution rates of up to 0.4 h−1, was investigated using a fermentor linked to a flow microcalorimeter. The weight specific rates of heat production and oxygen consumption showed a linear dependence on the dilution rate but diverged for higher rates due to glucose repression and wash out of the culture. With the media used, it was possible to almost completely determine the energy balance; the biomass formed contained about 60% of the produced energy and 40% was accounted for by heat production.
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    Applied microbiology and biotechnology 11 (1981), S. 212-215 
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    Notes: Summary The heat evolution of aerobic batch and chemostat cultures of growing yeast (Saccharomyces cerevisiae), in ethanol medium was investigated with a flowmicrocalorimeter. A balance for energy, carbon and oxygen was established in the chemostat cultures. Acetate which was presumably formed during the degradation of ethanol accounted for about 24% of the energy content of ethanol, but was not metabolized. Furthermore, only 45% the energy produced was stored in cell material, whereas 55% appeared as heat. From this and from the carbon balance it is concluded that the production of yeast cell material from ethanol is an exothermic process.
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    Applied microbiology and biotechnology 11 (1981), S. 226-228 
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    Notes: Summary Furfural, a Maillard reaction product, was found to inhibit growth and alcohol production by Saccharomyces cerevisiae. Furfural concentrations above 1 mg ml−1 significantly decreased CO2 evolution by resuspended yeast cells. Important glycolytic enzymes such as hexokinase, phosphofructokinase, triosephosphate dehydrogenase, aldolase and alcohol dehydrogenase were assayed in presence of furfural. Dehydrogenases appeared to be the most sensitive enzymes and are probably responsible for the observed inhibition of alcohol production and growth.
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    Notes: Abstract The activities of five hydrolytic enzymes in the culture filtrate and in cell-free extracts from strains of Streptomyces griseus, differing in macrotetrolide production, have been determined over a fermentation period of 200 h. The specific activities of phosphatase, phosphodiesterase, and adenosine triphosphatase in the medium, and phosphatase and phosphodiesterase in the cell-free extract were lower in the low than in the high producing strain. No significant difference was found between the strains, for adenosine triphosphatase and protease activity in the cell-free extract or protease activity in the medium. The specific activity of esterase was higher in the low than in the high producing strain.
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    Applied microbiology and biotechnology 11 (1981), S. 222-225 
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    Notes: Summary Batch cultures of Medicago sativa cells have been carried out in the dark under aerobic conditions using lactose as the sole carbon source. The stoichiometric analysis has been correlated with both the oxygen demand and the cell productivity in an oxygen-limited cultivation. The minimum oxygen transfer has been estimated to be 12.5 h−1, i.e., 0.3 v.v.m; this initial aeration rate led to cell necrosis. Starting with a low oxygen transfer coefficient kL·a and increasing the air flow rate during the course of fermentation gave an exponential growth phase. The maximum specific growth rate was 0.012 h−1 and the growth yield was 0.43 g.d.w./g. of lactose. On the basis of the mass-balance relation the maintenance coefficient and the maximum growth yield have been calculated.
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    Applied microbiology and biotechnology 11 (1981), S. 244-247 
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    Notes: Summary A method for the analysis of zearalenone, T-2 toxin, neosolaniol and HT-2 toxin from the grains of barley, wheat and oats has been developed. Toxins are extracted with ethyl acetate, purified on a kieselgel TLC-plate and analysed on a HPTLC-plate. The limits of detection are 0.2 mg/kg for zearalenone and T-2 toxin and 5 mg/kg for neosolaniol and HT-2 toxin. For more accurate estimation the purified toxins are analysed as their trimethysilyl derivatives by gas chromatography, in which the detection limit for all toxins in 50 μg/kg and the accuracy ±10%–30%. The percentage recovery in both methods is 80%.
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    Applied microbiology and biotechnology 12 (1981), S. 226-230 
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    Notes: Summary We have investigated the ability of intestinal microorganisms from the rat, guinea pig and man to carry out heterotrophic nitrification. We have shown that some intestinal isolates can oxidize acetohydroxamate and hydroxylamine to nitrite. Moreover, one of the isolates, Pseudomonas aeruginosa, exhibited the greatest nitrifying activity reported in the literature.
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    Notes: Summary The respiratory system, sporulation, and dynamics of alkaline protease formation were studied in three strains of the fungus Fusidium coccineum, differing in their ability to make antibiotics. Oxidative phosphorylation provided most of the energy in high and low activity strains and their respiratory activity was exclusively related to mitochondria functioning. In inactive and low activity strains, the terminal oxidation of reduced equivalents proceeds mainly by the respiratory chain with cytochrome oxidase as the terminal component. In the high activity strain there is a cyanide-resistant alternative pathway which is parallel to the classical cytochrome chain. The complete transition to the use of this pathway coincides with the stage of maximum antibiotic biosynthesis. The induction of the alternative pathway in the high activity strain was not concerned with the inhibition of the cytochrome site of the respiratory chain by fusidic acid. It was shown that the quantity of the antibiotic synthesized and the character of cellular differentiation can be altered by changing the oxidation pathwats used with inhibitors such as chloramphenicol and salicyl hydroxamate. We suggest that there must be common regulation of antibiotic formation, sporulation and induction of the alternative oxidation pathway.
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    Applied microbiology and biotechnology 12 (1981), S. 231-233 
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    Notes: Summary A new method is described measuring the methane-forming potentials of model disposals. The methane production of samples which were taken from lysimeters containing about 100 cbm of municipal waste material, was measured in laboratory experiments. The samples were filled in flasks and gassed with a mixture of H2/CO2 as a substrate for methane formation. A gaschromatograph with only a one-feet-column is used determining the quantity of the methane formed. Preliminary measurements show different methanogenic activities between “aerobic lysimeters” well supplied with oxygen and those under mainly anaerobic conditions.
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    Applied microbiology and biotechnology 12 (1981), S. 239-241 
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    Notes: Summary The moulds Aspergillus parasiticus (aflatoxins B1, B2, G1, G2, and M1), A. ochraceus (ochratoxin A) and Penicillium chrysogenum (citrinin) were grown on whole wheat bread either in the presence or absence of oxygen. In the presence of oxygen, both A. parasiticus and A. ochraceus developed dense colonies and formed considerable amounts of mycotoxins whereas Penicillium chrysogenum only grew and produced citrinin on the surface of the bread. In the absence of oxygen fungal growth did not occur and most of the toxins were undetectable even in regions of bread immediately adjacent to the moulds although a very slight diffusion of the aflatoxins B1 and G1 through 1 cm was observed. It is concluded that diffusion of the tested mycotoxins from hyphae into bread is not a problem for food safety.
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    Applied microbiology and biotechnology 12 (1981), S. 234-238 
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    Notes: Summary Microcalorimetrically determined heat production was used as parameter for microbial metabolism to study some aspects of anaerobic digestion. The heat production of sludge samples from a sufficiently active anaerobic digester is dependent upon the concentration of organic substances and is correlated with dehydrogenase activity. Microcalorimetric measurements were carried out to investigate the metabolisation of added substrates; ΔH-values of 150–270 kJ/M of cellobiose were determined for the digestion of cellobiose. Heat flow during the adaptation of digester sludge to cellobiose showed a dramatic change. The action of heavy metals on the microcalorimetrically determined metabolic activity of sludge samples was tested and we show that the addition of heavy metals, in concentrations often detected in waste water treatment, reduced the heat flow by up to 75%.
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    Applied microbiology and biotechnology 12 (1981), S. 242-247 
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    Notes: Summary Yeasts and moulds from 44 food samples were selectively enumerated on RBCC (Cooke's Rose Bengal/chlortetracycline/chloramphenicol) and OGY media (oxytetracycline/glucose/yeast agar). In regard to bacterial growth control, a combination of the two antibiotics proved to be superior to one. In tests with 18 mould and 14 yeast strains, the optimum inhibitory action of Rose Bengal was found to be at a concentration of 150 mg/l RBCC. Mould and yeast counts of 62 samples determined on RBCC — using inincreasing Rose Bengal concentrations up to 150 mg/l - and OGY media showed no difference; only the yeast count of samples of vegetables and meat, determined on RBCC medium containing 150 mg Rose Bengal per litre, showed a slight decrease. Application of the modified Rose Bengal medium enables an adequate control of bacterial growth and restricts mould colony size, facilitating a more rapid and accurate enumeration. This also holds for yeast colonies, which, in the absence of Rose Bengal, are very often covered by the mould colonies.
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    Applied microbiology and biotechnology 13 (1981), S. 1-9 
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    Notes: Summary The biomass yields (y) and COD reduction efficiencies (η) of a whey fermentation by Kluyveromyces fragilis were studied in a 100-1 fermenter at various stirrer speeds and lactose concentrations, and compared to those obtained in 10-1 and 15-1 fermenters at constant values of the oxygen transfer coefficient (kLa) and air velocity. The empirical models previously constructed by using the 15-1 fermenter data could be used to predict the yields on the other scales by calculating for each run the 15-1 fermenter which would provide the same oxygen transfer coefficient measured by the sulphite method on each fermenter under study. To make this model independent of stirrer speeds used in each generic fermenter, the effect of aeration and mixing was incorporated into an overall parameter (kLa) and the values of y and η were correlated only with temperature, lactose level and kL a, since these variables were approximately orthogonal. The validity of this model was finally checked against the yields reported by Wasserman et al. (1961) in a 6-m3 fermenter, thus confirming the capability of the model to provide a reliable basis for further scale-up on the production scale.
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    Applied microbiology and biotechnology 13 (1981), S. 19-23 
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    Notes: Summary Glucose oxidase (GOD) was immobilized on a nylon membrane. No activity of the GOD-nylon membrane was observed under normal conditions but it appeared when the membrane was mechanically stretched. A linear relationship was observed between the stress strength and the GOD activity of the membrane. The appearance of the GOD activity of the membrane with stress was reproducible and the membrane could be stored for at least 2 months. Therefore, the GOD-nylon membrane can be called a stress sensitive membrane.
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    Applied microbiology and biotechnology 13 (1981), S. 10-14 
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    Notes: Summary In this paper a new probe allowing the measurement of NAD(P)H-dependent culture fluorescence in a bioreactor is presented. This sterilizable probe can be inserted in every bioreactor using a standard fitting of 25 mm. Under well defined conditions high specificity and sensitivity as well as high stability are further advantages of this probe. Application examples are given to demonstrate the operation possibilities of this fluorescence probe. In batch growth the culture fluorescence can be used for on-line estimation of biomass concentration. Metabolic alterations due to substrate of oxygen deficiency can easily be detected by fluorometric measurements. In kinetic studies the fluorescence probe is of great use because of a very small time delay.
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    Applied microbiology and biotechnology 13 (1981), S. 15-18 
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    Notes: Summary The equilibrium oxygen concentration (C0) was determined in a complex fermentation media containing sucrose, lysine, molasses, corn steep liquor, antifoam agents and biomass. In simple systems, with all the components being dissolved, C0 represents the oxygen solubility and linearly decreases with increasing solute concentrations. In complex solutions with multi-phase structure an increase in C0 can be detected. It suggests that C0 consists of two components — one being oxygen solubility, the other being determined by the amount of oxygen adsorbed on the interphase and bound by macromolecules. The presence of biomass leads to a decrease in C0.
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    Applied microbiology and biotechnology 13 (1981), S. 24-28 
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    Notes: Summary In strain IGC 4052 of the amylolytic yeast Lipomyces kononenkoae growing in starch-limited chemostat cultures the critical dilution rate was reduced to about half of its theoretical value due to severe catabolite repression of amylase formation while its value in a repression-resistant mutant was near its theoretical value. The enzyme yield coefficients and the specific production rates of α-amylase and glucoamylase passed through maxima at intermediate dilution rates. The shapes of the respective curves were partly determined by catabolite repression (parent strain) or its absence (mutant strain) while induction did not seem to play to role. An additional growth-linked regulatory mechanism seemed to be involved. The use of continuous culture as compared with batch culture, increased the maximum biomass productivity by a factor of 2.2 in the mutant strain and by a factor of 1.4 in the parent strain.
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    Applied microbiology and biotechnology 13 (1981), S. 29-33 
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    Notes: Summary Fed-batch fermentations with Penicillum chrysogenum, strain S 3723, were fed with glucose as carbon source or with a mixture of glucose and acetic acid. When 20% of the carbon source was acetic acid, yields of penicillin-V were 25% higher than in fermentations where glucose was the only carbon source in the feed. The increased yield was due to higher specific productivity and/or cell mass. The effect was seen in fermentations where the carbon source was fed at a constant rate and the pH kept automatically at 6.5 by addition of inorganic acid or base, as well as in fermentations where pH controlled the addition of feed.
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    Applied microbiology and biotechnology 13 (1981), S. 34-38 
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    Notes: Summary The screening of twenty yeast strains for ethanol productivity at high osmotic pressure at temperatures ranging from 32°C to 45°C is described. Shake flask fermentations of 30°, 40°, and 50° Bx cane molasses were performed. The effect of temperature on productivity at a non-inhibitory ethanol level is weakly pronounced. Most strains fermented poorly at 50° Bx molasses but two Schizosaccharomyces pombe and one commercial baker's yeast, Saccharomyces cerevisiae performed well at all concentrations of molasses. In an extended study with Schizosaccharomyces pombe (CBS 352) and Saccharomyces cerevisiae (SJAB, fresh yeast), simulating a continuous run it was shown that Schizosaccharomyces pombe was less sensitive to high DS than Saccharomyces cerevisiae. At 25% DS the productivity of Schizosaccharomyces pombe is almost twice that of Saccharomyces cerevisiae.
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    Applied microbiology and biotechnology 13 (1981), S. 45-53 
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    Notes: Summary The growth parameters of Acinetobacter calcoaceticus, relevant to its mass cultivation on acetate and ethanol, were determined in batch and continuous culture experiments. Acetic acid exhibited a more powerful inhibitory effect on the growth rate than ethanol. In batch culture, the acetate component of an acetate-ethanol substrate pair was preferentially utilized, but diauxic growth as such was not evident. The temperature optimum for growth was in the region of 29°–36°C, and the cell yield did not change appreciably over this temperature range. In carbon-limited chemostat cultures, the maximum specific growth rates on acetate and ethanol were 1.22 h−1 and 0.96 h−1 respectively, and the respective yield coefficients were 0.4 and 0.75. A high maintenance energy requirement was exhibited, especially during acetate-limited growth. The respiratory quotient was dependent on the growth rate, the significance of which is discussed.
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    Applied microbiology and biotechnology 13 (1981), S. 39-44 
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    Notes: Summary The inhibitory influence of the higher concentration of 20butenal, crotonaldehyde was followed during the batch and long-term continuous fermentation of Candida utilis growing on synthetic ethanol. Most crotonaldehyde is removed from the medium by biotransformation. Crotonaldehyde inhibits the growth, lengthens the lag phase and decreases the biomass yield and the content of crude proteins in the biomass. The yeast C. utilis is capable of growing on media containing very high concentrations of inhibitor in the in-flow during continuous cultivation. Uncharacteristic transport oscillations of the content of crotonaldehyde were observed for which acidic groups on the cell membrane are probably responsible. A sensitive method which is suitable for measuring very low concentration of crotonaldehyde in aqueous solutions is described. Crotonaldehyde acts as an uncompetitive inhibitor with slight mixed type of inhibition. An equation describing the kinetics of inhibition was derived.
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    Applied microbiology and biotechnology 13 (1981), S. 60-61 
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    Keywords: Penicillin V ; fructification ; Bovista plumbea ; Pleurotus ostreatus
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    Notes: Abstract In our studies with the penicillin V acylase of Bovista plumbea strains NRRL 3501 and NRRL 3824, we wanted to receive spores of these fungi. Surprisingly the fruiting bodies obtained in our work were not identical with those characteristic for Bovista plumbea. We identified them as Pleurotus ostreatus. For this reason we have to correct the name of the fungi known as Bovista plumbea NRRL 3501 and NRRL 3824.
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    Applied microbiology and biotechnology 13 (1981), S. 54-59 
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    Notes: Summary In this work we discuss the aerobic biodegradation of sodium sulfite liquor of (NaSSL) and sodium lignosulfonate (NaLS) in a firwood sulfite waste liquor by a mixed culture of microorganisms consisting of two Trichosporon yeasts and bacteria in the Arthrobacter (two species), Pseudomonas and Chromabacterium genera. Under established process parameters, the NaSSL was biodegradated in one or two stages by mixed cultures. The kinetics in each stage was studied. The optimal ratio of NaLS and sugars in the substrate for the growth of mixed culture was determined. The growth of the monocultures of the bacteria on the NaLS and the growth of the yeasts as monocultures on the NaSSL substrate were examined. UV absorption and IR spectra were employed as analytical methods to follow the microbial degradation of NaLS. The aim of this research was to study the biodegradation process and kinetics and to remove by means of mixed culture the maximum amount of organic matter from NaSSL.
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    Applied microbiology and biotechnology 13 (1981), S. 62-63 
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    Notes: Summary In this study the gas chromatographic method of Poly-β-hydroxy butyric acid determination of Braunegg et al. (1978), was optimised for activated sludge samples. The poly-β-hydroxy butyric acid was extracted and quantified gravimetrically to confirm the accuracy of the gas chromatographic method. The authenticity of the extracted material was confirmed by several methods. It was also confirmed that the mixed liquor of an activated sludge process did not interfere with the esterification. The sample size required was 25 ml of mix liquor, or 50 mg of freeze-dried sludge.
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    Applied microbiology and biotechnology 13 (1981), S. 67-70 
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    Notes: Summary In modelling enzyme synthesis the Q-function has been generalized to describe ordinary induction and repression as well as mixed induction-repression. The practical use of the Q-function as found in the literature was considered, especially the implications of applying fractional exponents.
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    Applied microbiology and biotechnology 13 (1981), S. 64-66 
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    Notes: Summary The cultivation of Neurospora crassa, strain 74A, in Neurospora complete medium containing a azo dye, “Vermelho Reanil P8B” from Imperial Chemical Industries showed that after 24 h of contact, most of the dye was removed from the medium. The greatest extent of dye removal (91.3 to 89.1%) was achieved when the concentration of the dye was between 16.0 and 32.0 μg ml−1 which is the range found in industrial wastes. The biomass production was unaffected in the presence of the dye at all the concentrations analysed.
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    Applied microbiology and biotechnology 13 (1981), S. 71-76 
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    Notes: Summary The method of utilizing the principles of carbonate equilibrium chemistry to monitor the rate of inorganic carbon uptake by a variety of algal species is presented and discussed. The usefulness of this technique is demonstrated for both batch and chemostat algal culture. Data obtained from carbon limited batch and chemostat cultures suggest that the specific growth rate of a variety of algal species may best be represented as a Monod response to the free carbon dioxide concentration. The monitoring of carbonate equilibrium in the batch method provides a simple, rapid and inexpensive technique for obtaining rates of algal carbon fixation. This technique is well suited for obtaining the large volumes of detailed kinetic data necessary in building a basis for understanding the factors involved in algal productivity and algae species shifts, in both controlled and natural aquatic ecosystems.
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    Applied microbiology and biotechnology 13 (1981), S. 77-83 
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    Notes: Summary An investigation of the performance of air-lift fermenters showed that the value of the oxygen mass transfer coefficient (KLa) increased with both the aeration rate and vessel size. Although some change in the liquid circulation pattern occurred with increasing superficial gas velocity, there was no transition from bubbly to slug flow over the range of superficial gas velocities studied. Increases in broth viscosity caused an increase in gas hold up and a reduction in the values for KLa, although this reduction was not as great as that observed in mechanically agitated fermenters. Under conditions of aeration and agitation which gave comparable KLa values similar biomass yields of Aspergillus oryzae were obtained in 7.25 l and 100 l air-lift fermenters, and in a 3.5 l mechanically agitated fermenter.
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    Applied microbiology and biotechnology 13 (1981), S. 90-95 
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    Notes: Summary Cultivation of Hansenula polymorpha with substrate ethanol in a bench-scale tower loop reactor was simulated by means of a distributed parameter model with regard to the dissolved oxygen and substrate in the medium, oxygen and CO2 in the gas phase, and a lumped parameter model with regard to the cell mass. Space and time independence of the substrate and oxygen limiting constants of the Monod model, KS and KO, was assumed. Time variations of the yield coefficients, YX/S and YX/O, were allowed for.
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    Applied microbiology and biotechnology 13 (1981), S. 84-89 
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    Notes: Summary Cells of a Daucus carota suspension culture were entrapped in a matrix of calcium alginate. The immobilised cells, incubated in a buffer mixture of sucrose, nitrate, KCl, CaCl2, 2-(N-morpholino)-ethane sulphonic acid at pH 5.5, hydroxylated digitoxigenin. When compared under the same incubation conditions, freely suspended cells biotransformed digitoxigenin at a faster rate. Periplogenin formation was maximal at pH 5.3 and temperatures of 26°–34°C. The hydroxylase activity of the entrapped cells adapted to the presence of 20 mM CaCl2 over a 12 day incubation. The diffusion barrier established on entrapment of the cells could not be overcome by addition of detergents or methanol. Controlled addition of chloroform (at 1/4 and 1/2 saturation) did stimulate hydroxylation of digitoxigenin without adversely affecting cell viability. The rate of hydroxylation of digitoxigenin was linear over an immobilised cell concentration of 0–7 mg dry weight and a digitoxigenin concentration of 0–20 mg/L. Five consecutive batch bioconversions at a rate greater than 60% could be achieved before the biocatalyst was inactivated. The results are discussed in relation to improving the hydroxylation reaction by immobilised D. carota and other reactions performed by immobilised plant cells.
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    Applied microbiology and biotechnology 13 (1981), S. 102-106 
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    Notes: Summary Pseudomonas putida (ATCC 111 72) was studied in a continuous culture at various dilution rates with asparagine as the sole carbon source and limiting factor. Under the experimental conditions applied, a considerable number of the cells became attached to the fermentor walls and equipment. The viable count of the attached cells was of the same magnitude as those in suspension. The following steady-state characteristics were obtained: The cell-mass (OD620 and dry weight) versus dilution rate (D) had maxima at 0.63 and 1.1 h−1. The corresponding plot of viable count had a minimum at 0.94 h−1 whereafter it reached a maximum at 1.3 h−1. Largest yield coefficient obtained was 0.44 g dry weight/g asparagine (D=1.1 h−1). The productivity of the culture increased with D up to 1.1 h−1, which is far above the D corresponding to the maximum specific growth rate (μmax) of a batch culture (0.59 h−1). The cell mass was not completly washed-out of the fermentor even at a D of 2.2 h−1. The influence of attached growth for the steady-state characteristics, and the significance of the results in relation to chemostate as an instrument for testing environmental factors, are discussed. It is suggested that the attached cells had a significantly higher (μmax) value than the suspended ones.
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    Applied microbiology and biotechnology 13 (1981), S. 96-101 
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    Notes: Summary CO2 gas, evolved during alcohol fermentation using immobilized yeast, causes several undesirable problems in a packed-bed bioreactor installed vertically as it increases the dead space and causes hydrostatic pressure. In order to reduce this “CO2 gas phase effect” which lowers the efficiency of ethanol production, a shallow, horizontal packed-bed bioreactor has been developed with a free space above the gel bed. The horizontal packed-bed bioreactor was 1.5 times more productive than the vertical packed-bed bioreactor when operated continuously. Yeast cells immobilized in calcium alginate gel reached a steady state much quicker than those immobilized in polyacrylamide gels. In the horizontal packed-bed bioreactors, calcium alginate gel was also superior to polyacrylamide gel with respect to ethanol productivity. The profiles of both glucose and ethanol concentrations against axial sampling sites suggested that the horizontal packed-bed bioreactor was similar to a plug flow reactor. The mean gel size gradually increased upstream (1.9 mm to 3.3 mm). With the economic production of ethanol in view, the published data on different continuous alcohol production processes have been compared by plotting their productivities (y-coordinate) against the ethanol concentrations in the effluents (x-coordinate) for the dilution rate or space velocity at which the yield of ethanol from glucose was 95%. The horizontal packed-bed bioreactor has a very high performance which makes this bioreactor promising for the economic production of ethanol.
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    Applied microbiology and biotechnology 13 (1981), S. 113-116 
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    Notes: Summary Candida krusei is a harmful contaminant in baker's yeast manufacture, because it grows much faster than Saccharomyces cerevisiae under production conditions. This investigation showed that C. krusei utilizes the ethanol produced by baker's yeast as sole carbon source when molasses is used as a substrate. When the alcohol concentration in the effluent air is used as a parameter for controlling the aeration of the culture, conditions become favourable for the dominance of wild yeast because some of the ethanol produced by the baker's yeast is consumed immediately by C. krusei and aeration is then automatically reduced, leading to increased growth of the wild yeast.
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    Applied microbiology and biotechnology 13 (1981), S. 107-112 
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    Notes: Summary The activities of ACH1, NAD-ICDH, NADP-ICDH and CS were determined in cell extracts of high and low citric acid-producing strains of A. niger, cultivated on molasses medium by the surface or submerged method. A high differentiation in the activities of the enzymes studied was found to occur at various accumulation stages of citric acid and during its decomposition by moulds. During intensive citric acid synthesis, the activity of ACH and that of both dehydrogenases decreased significantly (though they did not disappear completely) compared to their initial activities during the growth period of the mycelium. CS activity, however, was maintained at almost the same level over the whole fermentation period or increased slightly, particularly in the case of low citric acid-producing strains. The relationships between the activities of these enzymes were reversed during citric acid decomposition by moulds. Moreover, it was shown that in the period of mycelium growth the maximal activities of the enzymes were much higher in submerged culture than in surface culture.
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    Notes: Summary Microbial growth during the wash-out phase has been described by an unstructured model based on Monod kinetics and the relation of linear substrate consumption. The optimal experimentation range and procedure have been evaluated for accurate estimation of the maximum specific growth rates.
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    Applied microbiology and biotechnology 13 (1981), S. 133-140 
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    Notes: Summary Glucose fermentation bySaccharomyces cerevisiae immobilized by entrapment in agar, carrageenan, alginate and polyacrylamide gels, was compared to that of freely suspended cells at concentrations of 10–50% (w.w.) sugar. The rate of ethanol production by the entrapped cells was 20–25% higher than that of the free cells. Concentrations of up to 14,5% w/w ethanol (30% glucose initial concentration) could be obtained. A number of hypotheses for the improved alcoholic fermentation are discussed.
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    Applied microbiology and biotechnology 13 (1981), S. 128-132 
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    Notes: Summary Biochemical removal of rust from iron surfaces has been investigated. By immersing a rusted iron plate in the culture medium of an iron-oxidizing bacterium, Thiobacillus ferrooxidans, iron adjacent to the rust was dissolved and the rust was peeled off. Since the amount of dissolved iron per unit iron plate surface area correlated with the concentration of ferric iron in the culture medium, the formation of ferric iron is probably involved in dissolving the iron as is the case for bacterial leaching. In the present study, rust removal in a “continuous” system in which the culture medium was circulated from the fermentor to the rust removal vessel and back again to the fermentor, has also been investigated. Although growth inhibition was observed with the formation of ferric iron precipitates during the operation in this system, it was possible to prevent this precipitation by lowering the pH of the medium during the mixed cultivation of T. ferrooxidans and a sulfur-oxidizing bacterium, T. thiooxidans.
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    Applied microbiology and biotechnology 13 (1981), S. 117-127 
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    Notes: Summary Biodegradability of straw is enhanced by its treatment with hot water. The soluble liquid produced contains high molecular-size LCCs as well as phenolic compounds and carbohydrates and can pose severe ecological problems. Fungal utilization of high molecular size LCC and the phenolics in such liquors were studied as carbon sources. A fungal strain, Aspergillus japonicus OM-4 was isolated on a high lignin, tannin medium. It degraded the lignin of the high molecular size soluble LCC efficiently and also many phenolic compounds, in the absence of additional carbon sources. The soluble LCC has potential for the isolation of other active lignin degraders. Hot aqueous extraction increased the degradability of straw by cellulases. Our isolate of A. japonicus degraded lignin in the straw faster and produced a more rapid increase in biomass than did other organisms tested. It degraded more than 40% of the lignin present in 20 days and also enhanced degradability of the carbohydrate of the straw by cellulolytic fungi.
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    Applied microbiology and biotechnology 13 (1981), S. 145-150 
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    Notes: Summary Using the model presented in part I, the measured time and spacial variations of process variables were simulated with satisfactory accuracy. Especially the experimentally found minima of the longitudinal dissolved oxygen concentration profiles in the substrate limiting growth range, which are caused by the transition from oxygen transfer limited to substrate limited growth along the tower, can be simulated with great accuracy.
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    Applied microbiology and biotechnology 13 (1981), S. 155-160 
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    Notes: Summary The rate of cortexolone 11α-, and 11β-hydroxylation by the mycelium ofCunninghamella elegans was much higher than that of its sporangiospores. In the course of the transformation, the sum of the free amino acid pools was not diminished in the spores where as it was decreased by 30–40% in the mycelium. The content of the nicotinamide nucleotides varied also in both forms of the microorganism. In the mycelium the NADP(H) pool was shown to be more reduced. The role of NADPH-generating system of the amino acid degradation and other regulation mechanisms in steroid hydroxylations by spores and mycelium ofC. elegans are discussed.
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    Applied microbiology and biotechnology 13 (1981), S. 184-187 
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    Notes: Summary Twenty-six yeast strains, representative of different yeast genera, were tested for their sensitivity to crude extracellular cellulolytic enzyme complexes obtained from the fungusTrichoderma reesei QM 9414 and its mutants M 6 and MHC 22 (Microcrystalline cellulose was the sole carbon source.) Practically all the yeast strains tested were found to be sensitive, exhibiting signs of cellwall weakening and lysis during prolonged incubation with the emzymes fromTrichoderma. Under growth conditions, the effect of cellulolytic enzymes on yeast cells and their growth rates was much less pronounced. However, at increased cellulase concentrations (5 mg/ml) in the growth medium, lysis of stationary phase yeast cells was observed.
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    Applied microbiology and biotechnology 13 (1981), S. 197-201 
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    Notes: Summary Glucose oxidase (GOD) was immobilized on an acetylcellulose membrane filter (pore size: 0.45 μm) with dipalmitoyl phosphatidyl-choline (DPPC). The activity of the GOD-DPPC membrane appeared during ultrasonic irradiation while the GOD activity disappeared when the irradiation was stopped. The apparent GOD activity (the value of the output current decrease of an oxygen electrode in the reaction mixture) gradually increased with increasing ultrasonic power below 3 W. On the other hand, it decreased with the increase in ultrasonic power over 4 W because dissolved oxygen in the reaction mixture in creased as ultrasonic cavitation was generated. The response of the membrane decreased with increasing ultrasonic frequency and the response of the membrane to ultrasound waves (20 KHz, 3 W) was reproducible. The membrane was stable for at least 2 months at 5°C. We conclude that the GOD-DPPC membrane can be regarded as a ultrasound sensitive membrane.
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    Applied microbiology and biotechnology 13 (1981), S. 202-207 
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    Notes: Summary Three tryptophan catabolites (tryptophol, indoleacetic acid and indoleacetaldehyde) were identified in the extracellular broths of deregulated mutants but not in that of the wild type. These compounds resulted from the degradation of excess tryptophan formed by the deregulated mutants. The mutants also produced 2 to 3 nonindolic compounds. Tryptophan was a minor product; tryptophol, the major broth metabolite. Among the deregulated strains, there were differences not only in the relative proportions but also in the spectra of the compounds produced. Tryptophol, indoleacetic acid and indoleacetaldehyde were produced by resting cells from added tryptophan or tryptamine. The presence of nonindolic compounds in the tryptophan-supplemented, but not tryptamine-supplemented, resting cell systems suggests that Hansenula polymorpha can degrade tryptophan by multiple pathways.
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    Applied microbiology and biotechnology 13 (1981), S. 222-225 
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    Notes: Summary Delignification of pine bark chips was observed after about 35 days when they were the sole carbon source in mixed liquid cultures of cellulolytic and lignin degrading strains of Bacillus and Cellulomonas. No delignification was observed in pure cultures. Free tannins liberated from the chips were also degraded in most of the cultures. The necessity of combining a cellulolytic and lignin-degrading bacterial strain to obtain delignification is discussed.
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    Applied microbiology and biotechnology 13 (1981), S. 236-241 
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    Notes: Summary The effects of pCO2 and pCH4 in the interval 0–1 bar on rates of acetate degradation and methane formation by methanogens as well as methane yields were studied in enrichment cultures in batch and continuous fermentations. In batch fermentations the rate of acetate utilization by methanogens was 1,000–1,500 mg/l · d at low levels of pCO2. CO2 was inhibitory and degradation rates were around 350 mg/l · d in 1 bar CO2. The degradation of acetate was almost linear. In continuous culture maximum rates of acetate utilization around 2,500 mg/l · d were obtained and the acetate concentration in the substrate was reduced by 98–99%. The yields of methane on acetate substrates were close to the theoretical value (1 mole CH4 per mole HAc) in the interval pCO2-0–0.5 bar. In 1 bar CO2 yields decreased by 20–30%. CH4 was found to be only slightly inhibitory; the inhibiting effects of 1 bar CH4 on acetate degradation rates were comparable to the effects of 0.3 bar CO2. Also gas sparging and rapid mixing had small effects compared with a non-sparged, slowly mixed culture. The redox potential was usually around −200 mV during fermentations and no connection was found between acetate degradation rate, Eh and pCO2. Acetate and propionate degradation were the reactions most sensitive to pCO2 and to obtain maximum rates as well as maximum methane yields pCO2-levels around 0.2 bar were found to be optimal.
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    Applied microbiology and biotechnology 11 (1981), S. 67-71 
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    Notes: Summary Application of an immobilized growing yeast cell system to continuous production of ethanol in high concentration (10%) was investigated using Saccharomyces cerevisiae IFO 2363. When a medium containing 25% glucose was fed, the growth of yeast cells in gel was inhibited. The inhibitory effect was found to be reduced by a stepwise increase in concentration of glucose in the feed medium. The stepwise operation resulted in constant growth of cells in the gel even in the medium containing 25% glucose. By this stepwise feeding system, continuous production of ethanol of 114 mg/ml was maintained at a retention time of 2.6 h for over 2 months and a conversion rate of glucose to ethanol of over 95% of theoretical, was achieved.
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    Applied microbiology and biotechnology 11 (1981), S. 72-77 
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    Notes: Summary Whole cells of Saccharomyces cerevisiae were immobilized in polyacrylamide gel. Consuming glucose, the immobilized cells produced glutathione from its constituent amino acids, and glutathione produced was excreted out of the gels. The conditions for immobilization of the yeast cells and for glutathione production were studied. Based on these data, the properties and the feasibility of the glycolytic pathway as an ATP regeneration system were discussed in reference to glutathione production.
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    Applied microbiology and biotechnology 11 (1981), S. 193-198 
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    Notes: Summary Lettuce thylakoids were immobilized by various methods selected to provide the chloroplast membrane with different environments. These included proteins (albumin and gelatin), polysaccharides (carrageenan and alginate gels) and synthetic polymers (photocrosslinkable resins and polyurethans). Large variations were observed in the activity yield after immobilization (ranging from 3% to 70%), in the storage stability (at 4°C in absence of light) and in the functional stability (continuous work at 20°C under illumination).
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    Applied microbiology and biotechnology 11 (1981), S. 241-243 
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    Notes: Summary The influence of moisture content and temperature during storage of grain on the formation of Fusarium metabolites was studied. Naturally and artificially contaminated barley grain samples were stored at 15%, 25%, and 30% moisture contents, and at temperatures of + 5°C + 25°C, and + 30°C. Time of storage varied between one week and six months and the occurrence of Fusarium species and metabolites was analysed. The only Fusarium metabolite detected was zearalenone. The extent of Fusarium contamination decreased during storage whilst the concentration of zearalenone increased. To avoid the danger of mycotoxicoses, grains must be dryed immediately after harvest and then stored at a low temperature.
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    Applied microbiology and biotechnology 11 (1981), S. 229-233 
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    Notes: Summary There are many methods of determining the activity of cellulolytic enzymes and numerous ways of expressing this activity. Since, however, the results obtained in different research centres are almost completely incomparable, an attempt has been made to introduce a uniform system for expressing a unit of enzyme activity. This system is based on the relationship between the degree of enzyme dilution and the enzyme activity. The slope coefficient “a”, determined experimentally, is constant for a given method of determing enzyme activities by reducing sugars irrespective of the substrate used, time of reaction or composition of cellulolytic complex. The presented method of expressing activities of cellulases and hemicellulases eliminates graphic descriptions which are very inconvenient in serial determination procedures.
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    Applied microbiology and biotechnology 11 (1981), S. 234-240 
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    Notes: Summary The filamentous fungus Aspergillus oryzae was found to grow well on the effluents produced during the extraction of palm oil. Biomass yields of approximately 50 g 100 g−1 organic matter were obtained containing 40% crude protein, with BOD reductions of 85% and COD reductions of 75% to 80% in batch culture following optimisation of growth conditions. Supplementation with an inorganic nitrogen source was found to be necessary (but not supplementation with phosphate or sulphate sources). The more resistant substrate constituents to biodegradation were water soluble carbohydrate and nitrogenous material, possibly Maillard reaction products, and polyphenols.
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    Applied microbiology and biotechnology 11 (1981), S. 248-252 
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    Notes: Summary Various extracts obtained from different phases of composting municipal garbage were tested for their effect on the growth of Bacillus megaterium and a mixed bacterial population. The results showed that antimicrobial substances are present in the fresh garbage. Their biocidal efficiency decreases during the rotting process and no new antimicrobial substances are produced during rotting. The evolution of heat as well as a certain kind of detoxication is important for the sanitation of garbage by the composting process.
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    Applied microbiology and biotechnology 12 (1981), S. 1-5 
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    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A blue-green algae, Anabaena N-7363, was immobilized in 2% agar gel. The hydrogen productivity of the immobilized algae was three times higher than that of free algae. The maximum hydrogen production rate by the immobilized blue-green algae was 0.52 μ moles h−1 g−1 (of wet gel) in the medium without nitrogen sources under illumination (10,000 lux). The oxygen evolved was then removed by a reactor containing aerobic bacteria. A photo-current of 15–20 mA was continuously produced for 7 days by the photochemical fuel cell system consisting of the immobilized Anabaena reactor, the oxygen-removing reactor and the hydrogen-oxygen fuel cell. The conversion ratio of hydrogen to current was from 80% to 100%.
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  • 91
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    Applied microbiology and biotechnology 12 (1981), S. 6-9 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Of four chemical methods for estimating mycelial biomass in koji fermentation which were examined, the modified method of Ride and Drysdale, was found to be most suitable. The observed level of aldehyde, expressed as glucosamine, is related to fungal dry weight. The assay method correlates chitin levels with some enzyme activities in the fermentation. This method may be applicable for detecting the extent of fungal growth in other solid and semi-solid substrates.
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  • 92
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    Applied microbiology and biotechnology 12 (1981), S. 10-15 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The behaviour of Saccharomyces cerevisiae cells entrapped in a polyacrylamide gel was studied during their continuous function in an ethanol-producing reactor. Polymerization destroys 40% to 80% of the cells, depending on their physiological state. A three day adaptation phase is required before ethanol production stabilizes and this phase corresponds to an increase in cell concentration in the gels and to protein synthesis. The amounts of DNA, glucan, glycogen and trehalose are different in entrapped and free cells. Microscopic observation shows that 75% to 85% of the cells lose their integrity and that the remainder appear to multiply normally. Within a gel particle, both viability and fermentation activity are heterogeneous. A high percentage of cells have low viability and low fermentation activity. A proportion of cells remains capable of forming colonies and these cells have higher fermentation activity and are preferentially localized at the surface of gel particles.
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  • 93
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    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The cellulolytic enzyme complexes secreted by the fungus Trichoderma reesei QM 9414 and its mutants M 5, M 6, MHC 15, and MHC 22 were characterized by determining their specific filter-paper (FP)-, carboxymethylcellulase (Cx)-and β-glucosidase (βG)-activities. They were characterised further by measuring their Cx and βG profiles after separation on an isoelectrofocusing column over the pH range 3–10. While the overall FP-activity was roughly equal in all preparations, the specific β-glucosidase activity was highest in mutants MHC 15 and MHC 22 which are distingiushed morphologically from the parent strain, QM 9414, by a higher degree of branching of their hyphae. Two peaks of β-glucosidase activity were detected by isoelectric focusing in preparations from QM 9414 and M 6, none in the enzyme from the mutant M 5 while 3 and 4 peaks respectively were found in preparations from morphological mutants MHC 15 and MHC 22. The higher β-glucosidase activity in these last two preparations was also reflected in the higher glucose to cellobiose ratio in the initial stages of cellulose hydrolysis by the individual enzyme preparations.
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  • 94
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    Applied microbiology and biotechnology 12 (1981), S. 36-38 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Four out of thirty-one algae strains belonging to the order Chlorococcales exhibited good growth on solid media containing n-alkanes. Chlorella vulgaris (397) was able to degrade n-tridecane in cooxidation. The corresponding secondary alcohols and ketones in C2-to C7-position could be identified in the culture broth. The same oxidation products could be found in the media of cultures grown in darkness with the addition of glucose. This demonstrates a subterminal degradation pathway of C. vulgaris. There was no indication for a mono-or diterminal oxidation of alkanes by algae. The fatty acid pattern of lipids exhibited an incease in long chain acids and a decrease in shorter chain acids. The growth rate of cells grown on alkanes increased after 72 h, but the release of autospores was retarded.
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  • 95
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary To develop a large-scale isolation of leucine dehydrogenase (E.C. 1.4.1.9) as industrial catalyst we carried out a limited screening for microorganisms with high leucine dehydrogenase activity. Conditions for the growth and enzyme formation of Bacillus sphaericus (DSM 396) which proved to be the best enzyme producer were optimized. The highest yield in volume and specific activity were obtained using glucose and yeast-extract in the medium. The highest specific enzyme activity was found at the end of the exponential growth phase. Cultivation of Bacillus sphaericus under optimal conditions increased the yield to about 3 U mg−1. The heat stability of the enzyme was exploited to develop a simple large-scale purification. Together with an ultrafiltration step, the enzyme could be enriched 9fold in a short time. After further purification using DE-cellulose an enzyme preparation (25fold enriched) was obtained; suitable as a technical catalyst in amino acid production.
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  • 96
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    Applied microbiology and biotechnology 12 (1981), S. 28-35 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Optimal growth of Methanosarcina barkeri occurred in a defined medium containing methanol when 2.5–4 mM sodium sulphide was added giving a concentration of 0.04–0.06 mM dissolved sulphide (HS−+S2−. When the sulphide concentration was too low for optimal growth (e.g., 0.1 mM Na2S added) the addition of the redox resin ‘Serdoxit’ acted as a sulphide reservoir and caused a significant stimulation of growth. Furthermore it could be demonstrated that iron sulphide, zinc sulphide or L-methionine could also act as sulphur sources while the addition of sodium sulphate to sulphide-depleted media failed to restore growth. The amino acid L-cysteine (0.85 mM) stimulated growth but could not replace Na2S. Under optimal cysteine-and sulphide concentrations the generation time of this strain was about 7–9 h during growth on methanol, giving a growth yield of about 0.14 g/g methanol consumed. Different M. barkeri strains were also able to grow under these conditions on acetate (30–50 h doubling time) without a significant lag-phase and with complete substrate consumption even though the inoculum was grown on methanol or H2−CO2. When methanol and acetate were present as a mixture in the medium both were used simultaneously.
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  • 97
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    Applied microbiology and biotechnology 12 (1981), S. 46-52 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Statistically designed experiments were used to identify variables important in the 7α-dehydroxylation of cholic acid to deoxycholic acid by strains of Clostridium bifermentans in pH-controlled anaerobic fermentation. Deoxycholic acid yields were highest in the presence of 10% CO2 and near pH 7 but were largely unaffected by the strain of organism used, time of bile acid substrate addition, mode of gas delivery, presence of thioglycollate, or the use of OH− ion or HCO 3 − ion for pH control. However, dehydroxylation was enhanced, and the redox potential remained relatively high, when temperatures were low, inoculum size small, and growth inhibitors were present. Deoxycholic acid yields of up to 40% were observed but the formation of 7-ketodeoxycholic acid side product could not be entirely prevented.
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  • 98
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    Applied microbiology and biotechnology 12 (1981), S. 39-45 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A gaseous hydrocarbon-assimilating microorganism, Nocardia corallina, grew on 1-alkenes (C3, C4 and C13 to C18) and produced corresponding 1,2-epoxyalkanes. One of the products, 1,2-epoxytetradecane, had a positive rotation [α] D 20 =+8.6°. The concentration of propyleneoxide reached 0.6 g/l after 5 days of cultivation. Accumulation of 1,2-epoxytetradecane continued till the end of cultivation when the pH was not controlled, though production stopped in a 24 h cultivation when the pH was controlled at an optimum pH for growth. Propylene-grown cells produced 1,2-epoxytetradecane from 1-tetradecene and degraded tetradecane. In the presence of chloramphenicol, propylene-grown cells did not degraded tetradecane though 1,2-epoxytetradecane was produced from 1-tetradecene. A spontaneous mutant, which neither grew on propylene nor produced propyleneoxide, was isolated. This strain grew on tetradecane and 1-tetradecene but produced only a trace amount of 1,2-epoxytetradecane from 1-tetradecene.
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  • 99
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    Applied microbiology and biotechnology 12 (1981), S. 53-57 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Changes in the amount of nucleic acid and nitrogen, and the relationships between these amounts and the growth rate of tobacco cells (Nicotiana tabacum L. cv. Bright Yellow-2) at different initial nitrogen concentrations in the medium, were examined in batch cultures. During culture in basal medium, the amount of intracellular nucleic acid expressed per unit of dry biomass was 36.3 mg RNA g−1 cell and 8.1 mg DNA g−1 cell at the beginning of batch culture. These values increased 2.5 fold for RNA and 1.5 fold for DNA during the exponential growth phase and then gradually decreased with the decline in the growth rate. Similar changes were also observed in the medium containing less nitrogen. The specific growth rate, μ (day−1), of the culture corresponded to the magnitude of the intracellular RNA content (mg RNA g−1 cell), and the linear relationship, RNA=38μ+23 was obtained. In addition, there were remarkable positive correlations between the total and protein nitrogen, and μ during the cultures. The mononucleotide composition of total RNA (AMP+UMP)/(GMP+CMP) which was suggested to be a convenient index of metabolic activity was nearly constant (0.78 to 0.80) during tobacco cell culture in the basal medium.
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  • 100
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    Applied microbiology and biotechnology 12 (1981), S. 58-62 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A method for the cultivation of Pleurotus sajorcaju on a relatively large scale using cotton waste as substrate has been developed, and the mushroom so obtained has higher protein content than and comparable carbohydrate content to Agaricus bisporus, Volvariella volvacea, Lentinus edodes and Pleurotus ostreatus. The crude fats, ash, energy value, vitamin and mineral contents are lower and yet the differences are not great. The biological efficiency from cotton waste compost is lower than that from straw compost, however, the former has the advantage of giving rather even yield over successive flushes. This mushroom has a high potential to be produced economically on a large scale in Hong Kong.
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