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  • 1990-1994  (14)
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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 71 (1990), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract Aspergillus nidulans produces an extracellular invertase when incubated in the presence of sucrose and about half of the activity produced was found to be associated with the mycelium. Sixty percent of this mycelial invertase could be solubilised by simple mechanical disruption. Among the agents tested for solubilisation of invertase, proteinase K and dithiothreitol were the most effective.
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  • 2
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Protoplasts prepared from cultured albinoid cells of petunia do not express photosynthetic genes, such as those coding for chlorophyll a/b-binding (Cab) proteins or ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco). They therefore provide a convenient system for expressing recombinant photosynthetic genes, without background interference. Transfection of petunia protoplasts with vectors bearing the Lhcbl*1 Cab gene under the control of the 35S promoter of cauliflower mosaic virus (CaMV) resulted in the appearance of significant amounts of the specific transcripts, but not of the corresponding polypeptides, as inferred from northern and western blot analysis, respectively. The use of an expression vector carrying the translational enhancer Ω of tobacco mosaic virus (TMV) strongly enhanced the appearance of transfected gene products: western blot analysis of transfected protoplasts clearly revealed the appearance of Lemna gibba Lhcbl*1 and Lhcb2*1, tomato Lhcb2*1 and psaD, and pea rbcS gene products. Molecular weight estimations of the newly synthesized polypeptides indicated that each was promptly processed into its mature-cleaved form within the transfected albinoid protoplasts. This occurred despite a lack of chlorophyll and the absence of a thylakoid network.
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  • 3
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: To study the biogenesis of the photosynthetic apparatus in corollas, as well as compositional differences between corolla and leaf chloroplasts, the levels of 12 nuclear- and plastid-encoded thylakoid and stromal components were analyzed by western blotting using heterologous antisera. Relative levels of the thylakoid polypeptides analyzed in petunia (Petunia hybrida cv. Hit Parade Rosa) and carnation (Dianthus caryophyllus cv. White Sim) corollas increased, per unit chlorophyll, in parallel to corolla development, peaking at the mature stage in both flower types, with the exception of subunit V of the photosystem I (PSI) core complex, which continued to accumulate even after anthesis. The photosystem II (PSII) major light-harvesting chlorophyll a/b protein accumulated in corollas to a level, per unit chlorophyll, similar to that in leaves in both petunia and carnation plants. Components of the cytochrome b6/f complex were found to accumulate to higher levels in corolla chloroplasts than in leaves. The opposite trend was found for components of the PSI core complex, as well as for the stromally located small and large subunits of ribulose-1,5-bisphosphate carboxylase, which accumulated in corollas to levels ca 2. 5 times lower than their respective levels in leaves. The latter subunits accumulated coordinately in corollas of both plant types during flower development. Data obtained from immunological studies were correlated with those at the mRNA level. Nothern blotting revealed that, in petunia corollas, the steady-state transcript level of genes coding for the small subunit of ribulose-l,5-bisphosphate carboxylase was identical to that of genes coding for the major light-harvesting chlorophyll a/b protein. Levels of both transcripts, as well as those of plastid-encoded genes for the PSII reaction center's Dl and D2, were ca two-thirds of their respective levels in leaves. In contrast, the level of transcript for the large subunit of ribulose-1,5-bisphosphate carboxylase was reduced 5-fold in petunia corollas, as compared to leaves.
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Physiologia plantarum 78 (1990), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Corollas of Petunia hybrida (cv. Hit Parade Rosa) flowers fixed 14CO2 under both light and dark conditions. Rates of light fixation were much higher in mature pink corollas than in young, green corollas [57 and 9 nmol (ngchl)1 min-1], paralleling the development of chloroplasts in these tissues. Stomatal conductance in corollas was only 12% of that in green leaves, mainly due to the presence of few, and non-functioning stomata in the corolla. The activity and concentration of ribulose bisphosphate carboxylase (EC 4.1.1.39) in corolla extracts were only about 30% (per unit Chi) of those in extracts from green leaves. These results, together with previous results, might indicate a coordinated reduction in activity of systems participating in photosynthesis in corollas. The fixation products following a 6 s pulse with 14CO2, were typical of C, plants in both corollas and green leaves, but a higher level of β-carboxylation products was found in the corollas. The activity of phosphoenol-pyruvate carboxylase (EC 4.1.1.31) (per unit protein) was similar in both tissues. Although the total carbon fixed by the corolla constituted only a small part of the metabolites required for flower development, certain photosynthetic metabolites might have a regulatory role in flower development.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Current genetics 21 (1992), S. 23-26 
    ISSN: 1432-0983
    Keywords: Trichoderma ; Transformation ; Hygromycin B resistance ; Benomyl resistance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary We have developed a transformation system for Trichoderma hamatum and Trichoderma harzianum Rifai, using dominant markers for selection based on the Escherichia coli hygromycin B phosphotransferase gene (hph) and the β-tubulin gene (bml) from Neurospora crassa, respectively. Transformation frequencies and protoplast regeneration were low in both species. All the T. hamatum hygromycin-resistant transformants analysed were mitotically stable, in contrast to those of T. harzianum derived by benomyl resistance, in which only 50% of the transformants analysed were stable. Molecular analysis of transformants showed the integration of the transforming DNA into the genome and indicated that the number and sites of integration varied among the transformants.
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  • 6
    ISSN: 1432-0983
    Keywords: Aspergillus niger ; Invertase ; Purification ; Sequence
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A secreted invertase was purified 23-fold by ultrafiltration, ion-exchange, and gel filtration chromatography from the culture supernatant of 18h sucrose-grown cultures of Aspergillus niger. The purified enzyme hydrolysed sucrose and raffinose but there was no detectable hydrolysis of inulin, melezitose or PNPG. Invertase activity was optimal at pH 5.5 and 50°C. The molecular mass of reduced invertase was 115 kDa, as determined by SDS gel electrophoresis. The native molecular weight of between 225 kDa and 250 kDa, estimated by electrophoresis under non-denaturing conditions, suggests that the protein is a dimer of identical subunits. The suc1 gene encoding this protein was completely sequenced. The translated sequence yields a protein of 566 amino acids with a calculated molecular mass of 61 kDa, suggesting that carbohydrates represent about 50% of the mass of the protein.
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  • 7
    ISSN: 1573-5060
    Keywords: carnation ; DNA fingerprints ; minisatellites ; relatedness
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary DNA fingerprinting analysis of genetic relatedness between carnation genotypes using human derived minisatellite probes, correctly reflected relationships within and between categories of carnation plants with inferred relatedness. Similar DNA fingerprint patterns were observed between genotypes within either ‘standard’ or ‘spray’ categories. A high level of similarity was also detected between those categories. Moderate similarities were found within the ‘dwarf’ category, and between ‘dwarf’ and either ‘standard’ or ‘spray’ categories. Large differences were observed between a wild species and cultivated categories. Abbreviations: b.1.-breeding line, BS-band-sharing
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  • 8
    ISSN: 1573-5060
    Keywords: breeding ; Carica papaya ; DNA markers ; genetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Various DNA fingerprint probes were applied to Carica papaya and other Carica species for both identification and genetic analysis. Each of the Carica papaya cultivars is characterized by a specific DNA fingerprints pattern. Various Carica species also have specific patterns which distinguish them from one another. Band sharing levels were used to estimate the relatedness between the various Carica species. Genetic analysis of 11 progeny from a cross between the Carica papaya cultivars 17/82 and 112 suggests that application of DNA fingerprinting to Carica papaya breeding, could make the process more efficient. Genetic analysis of the DNA fingerprint bands revealed no linkage or allelic relationship among the bands analyzed, indicating that these loci are not clustered in the Carica genome.
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  • 9
    Publication Date: 1992-01-01
    Print ISSN: 0172-8083
    Electronic ISSN: 1432-0983
    Topics: Biology
    Published by Springer
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  • 10
    Publication Date: 1993-07-01
    Print ISSN: 0172-8083
    Electronic ISSN: 1432-0983
    Topics: Biology
    Published by Springer
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