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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology ecology 15 (1994), S. 0 
    ISSN: 1574-6941
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract Several soil and subsoil samples from a soil accumulation and from the aquifer of a site of a former pesticide production factory, which were contaminated with chlorinated benzenes (CB), chlorinated phenols (CP) and hexachlorocyclohexanes (HCH) were investigated chemically for their content of individual pollutants, and microbiologically for the presence and the activity of different microorganisms. The samples of the soil accumulation (until 2 m depth) showed a higher content of chlorinated organic compounds (〉 1000 mg extractable halogenated organic substances (EOX) kg−1 soil; ratio CB:HCH:CP = 88:10:2), than the samples from the aquifer (〈 150 mg EOX kg− soil; ratio CB:HCH:CP = 88:6:6). All isomers of CB and CP, and the five important isomers of HCH could be detected in the samples. In samples of the accumulation, 1,2,3,4,-tetrachlorobenzene and pentachlorobenzene were the dominant CB in the upper layers, and 1,2,4-trichlorobenzene in the lower layers. In almost all samples α-HCH was predominant (〉 50%) among the HCH. The major pollutant of samples from the aquifer was 1,2,4-tricholorobenzene (〉 50% of CB). Among the HCH, δ-HCH was predominant, with only three exceptions. Degradation experiments with mixed bacterial cultures showed the aerobic degradation of monochlorobenzene, 1,3- and 1,4-dichlorobenzene, 1,2,4-trichlorobenzene, 1,2,3,4- and 1,2,4,5-tetrachlorobenzene 1,2,3-tricholorobenzene only in combination with 1,2,4-trichlorobenzene, and α-HCH, whereas 1,2-dichlorobenzene, 1,3,5-trichlorobenzene, β-HCH, 4-chlorophenol, and 2,4,5-trichlorophenol were not significantly transformed. It should be stressed that the compounds which were biodegraded in the laboratory were present in relatively high concentrations in situ, indicating limiting factors in their in situ degradation. Soil and subsoil microorganisms were present in numbers up to 105 colony forming units (CFU) g−1 soil. In soil samples, Gram-positive bacteria (coryneforms and Bacillus spp.) were dominant, mainly in the upper layers, but in the subsoil samples of the aquifer the majority of isolates were Gram-negative and could be identified as Pseudomonas stutzeri, Ps. fluorescens, Aeromonas sp. and Acinetobacter sp. The degradation potential observed under laboratory conditions should be studied further under in situ conditions to assess the success of a bioremediation.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology ecology 23 (1997), S. 0 
    ISSN: 1574-6941
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Different applications of the activated sludge treatment process are employed globally for the biological treatment of wastewater. Since the activated sludge process was first developed, different kinds of sedimentation problems, in particular bulking sludge and foaming, have been observed and it is widely accepted that extensive, uncontrolled growth of filamentous bacteria is the main cause of these difficulties. Since the pioneering work of Eikelboom and coworkers who characterized and described seven groups of 26 morphological types of filamentous organisms several attempts have been made to develop new methods for isolation, cultivation and identification of the isolates. Improvement has also been sought in the methods for direct detection, to allow a better understanding of the complex phenomena of sludge bulking and foaming. However, although knowledge of the phylogeny of filamentous organisms has increased recently, only a few attempts have been made to achieve a better understanding of their growth characteristics. The aim of this paper is to give an overview of detection and cultivation methods with special emphasis on the comparison of classical approaches with the modern molecular biological methods, including in situ detection and identification of filamentous bacteria.
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology ecology 52 (2005), S. 0 
    ISSN: 1574-6941
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Methane cycling within compost heaps has not yet been investigated in detail. We show that thermophilic methane oxidation occurred after a lag phase of up to one day in 4-week old, 8-week old and mature (〉10-week old) compost material. The potential rate of methane oxidation was between 2.6 and 4.1 μmol CH4 (gdw)−1 h−1. Profiles of methane concentrations within heaps of different ages indicated that 46–98% of the methane produced was oxidised by methanotrophic bacteria. The population size of thermophilic methanotrophs was estimated at 109 cells (g dw)−1, based on methane oxidation rates. A methanotroph (strain KTM-1) was isolated from the highest positive step of a serial dilution series. This strain belonged to the genus Methylocaldum, which contains thermotolerant and thermophilic methanotrophs. The closest relative organism on the basis of 16S rRNA gene sequence identity was M. szegediense (〉99%), a species originally isolated from hot springs. The temperature optimum (45–55 °C) for methane oxidation within the compost material was identical to that of strain KTM-1, suggesting that this strain was well adapted to the conditions in the compost material. The temperatures measured in the upper layer (0–40 cm) of the compost heaps were also in this range, so we assume that these organisms are capable of effectively reducing the potential methane emissions from compost.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 107 (1993), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract Eleven isolates obtained from a laboratory sewage treatment plant, most of them presumptively assigned to the coryneform genera Curtobacterium and Aureobacterium were studied for the presence of intracellular polyphosphates and polyphosphate dependent enzymes. All isolates stored polyphosphates and showed adenylate kinase activities ranging from 64 to 815 mU mg−1. Polyphosphate:AMP phosphotransferase could only be detected in one isolate. Three isolates showed a polyphosphate kinase activity also in minor amounts from 15 to 17 mU mg−1. A polyphosphate dependent NAD or 3-phosphoglycerate kinase could not be detected. Polyphosphate glucokinase activity was measured in cell-free extracts of nine isolates ranging from 2 to 376 mU mg−1. Three isolates showed in addition to the polyphosphate glucokinase, a glucose-6-phosphate-dependent NAD kinase. For the regeneration of NADP from NAD and polyphosphate, this enzyme system may give the isolates a distinct competitive advantage, especially for anabolic processes. The polyphosphate-dependent enzymes reported here may play an additional role in the complex process of ‘biological’ phosphate removal from wastewater.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1476-5535
    Keywords: biodegradation ; fuel oil ; bacterial cultures ; activated sludge
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary This study examined the microbial degradation of fuel oil by nine highly adapted different commercially available mixed bacterial cultures (DBC-plus™, Flow Laboratories, Meckenheim, F.R.G.) and a bacterial community from a domestic sewage sludge sample. All mixed cultures were cultivated under aerobic batch conditions shaking (110 rpm) at 20°C in a mineral base medium containing 1 or 5% (v/v) fuel oil as the sole carbon source. Percent degradation of fuel oil and the n-alkane fraction was recorded for the nine DBC-plus cultures and the mixed population of the activated sludge sample. The increase in colony counts, protein, and optical density was studied during a 31-day incubation period for DBC-plus culture A, DBC-plus culture A2 and the activated sludge sample. The activated sludge mixed culture was most effective in degrading fuel oil, but various isolated bacterial strains from this bacterial community were not able to grow on fuel oil as the sole carbon source. In contrast, the n-alkane degradation rates of the DBC-cultures were lower, but single strains from the commercially available mixed cultures were able to mineralize fuel oil hydrocarbons. Strains ofPseudomonas aeruginosa were isolated most frequently and these organisms were able to grow very rapidly on fuel oil as a complex sole carbon source. The results indicate that fuel oil degradation in domestic sewage sludge is performed by mixed populations of naturally occurring bacteria and does not depend on the application of highly adapted commercially available cultures.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Applied microbiology and biotechnology 37 (1992), S. 529-531 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The anaerobic degradation of p-cresol under denitrifying conditions by a bacterial consortium was studied in batch and continuous cultures. Concentrations up to 3 mm were degraded within 5–6 days with 4-hydroxybenzyl alcohol, 4-hydroxybenzaldehyde and 4-hydroxybenzoate as intermediates. Steady states could be maintained at only one dilution rate, D=0.04 h−1. A further increase in the dilution rate to 0.0 8 h−1 resulted in culture wash-out. An estimation of the Saturation constant was made (〈1 mg/l), taking the maximum specific growth rate as 0.045 h−1, thus yielding a value of 0.125 mg p-cresol/l.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Applied microbiology and biotechnology 37 (1992), S. 524-528 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The anaerobic degradation of phenol under denitrifying conditions by a bacterial consortium was studied both in batch and continuous cultures. Anaerobic degradation was dependent on NOf3 p− and concentrations up to 4 mm phenol were degraded within 2–5 days. During continuous growth in a fermenter, steady states could be maintained at eight dilution rates (D) corresponding to residence times between 12.5 and 50 h. Culture wash-out occurred at D=0.084 h−1. The kinetic parameters obtained for anaerobic degradation of phenol under denitrifying conditions by the consortium were: maximam specific growth rate = 0.091 h−1; saturation constant = 4.91 mg phenol/l; true growth yield = 0.57 mg dry wt/mg phenol; maintenance coefficient = 0.013 mg phenol/mg dry wt per hour. The Haldane model inhibition constant was estimated from batch culture data giving a value of 101 mg/l. The requirement of CO2 for the anaerobic degradation of phenol with NOf3 p− indicates that phenol carboxylation to 4-hydroxybenzoate was the first step of phenol degradation by this culture. 4-Hydroxybenzoate, proposed as an intermediate of phenol carboxylation under these conditions, was detected only in continuous cultures at very low growth rates (D=0.02 h−1), but was never detected as a free intermediary metabolite either in batch or in continuous cultures.
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  • 8
    ISSN: 1432-184X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In the course of an in situ bioremediation, different hydrologically controllable test plots were installed on the ground of a waste-oil contaminated site, and continuously injected with nutrient solution and the electron acceptors NO3 −, O2, and H2O2. In a two-year period, groundwater samples obtained from different recovery wells within these field plots, in addition to subsoil samples, were monitored for several chemical and microbiological parameters. The removal of hydrocarbons observed in the water samples could not unambiguously be attributed to biodegradation, and was probably caused by groundwater treatment measures. However, chemical (gaschromatographic) and microbiological data from the subsoil samples indicated a biological degradation of pollutants. Analysis of the groundwater samples of the different test plots revealed only minor quantitative differences. With time, only a slight increase in bacterial numbers on different media, including hydrocarbon-agar, was observed. In general, chemical and microbiological analyses of groundwater samples cannot replace analyses of subsoil samples for a sufficient documentation of in situ remediation processes in subsoil. From the groundwater and subsoil samples, 3,446 pure cultures, obtained from R2A agar, were characterized morphologically and physiologically, and identified in order to study the culturable bacterial communities. Several qualitative differences in composition and diversity of the bacterial communities among the test plots were observed. More than 70 different species or taxonomic groups (most of them known as hydrocarbon degrading taxa) could be identified from the groundwater samples; these were mainly the Gram-negative genera Acinetobacter, Alcaligenes, Comamonas, Hydrogenophaga, Pseudomonas, Flavobacterium/Flexibacter/Cytophaga, and others. A high proportion of Gram-positive organisms (42.5%), belonging to Bacillus and the various genera of coryneform and nocardioform organisms, were isolated from the subsoil samples.
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  • 9
  • 10
    Publication Date: 1995-06-01
    Print ISSN: 0043-1354
    Electronic ISSN: 1879-2448
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Published by Elsevier
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