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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Biology and fertility of soils 32 (2000), S. 310-317 
    ISSN: 1432-0789
    Keywords: Key words Critical sulphur concentration ; Sulphur requirement ; Microbial biomass ; Glucose ; Cellulose
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract  The critical S concentration and S requirement of the soil microbial biomass of a granitic regosol was examined. S was applied at the rate of 0, 5, 10, 20, 30 and 50 μg S as MgSO4·7H2O, together with either 3000 μg glucose-C or 3333 μg cellulose-C, 400 μg N, and 200 μg P g –1 soil and 200 μg K g–1 soil. Microbial biomass, inorganic SO4 2–-S, and CO2 emission were monitored over 30 days during incubation at 25  °C. Both glucose and cellulose decomposition rates responded positively to the S made available for microbial cell synthesis. The amounts of microbial biomass C and S increased with the level of applied S up to 10 μg S g–1 soil and 30 μg S g–1 soil in the glucose- and cellulose-amended soil, respectively, and then declined. Incorporated S was found to be concentrated within the microbial biomass or partially transformed into soil organic matter. The concentration of S in the microbial biomass was higher in the cellulose- (4.8–14.2 mg g–1) than in the glucose-amended soil (3.7–10.9 mg g–1). The microbial biomass C:S ratio was higher in the glucose- (46–142 : 1) than in the cellulose-amended soil (36–115 : 1). The critical S concentration in the microbial biomass (defined as that required to achieve 80% of the maximum synthesis of microbial biomass C) was estimated to be 5.1 mg g–1 in the glucose- and 10.9 mg g–1 in the cellulose-amended soil. The minimum requirement of SO4 2–-S for microbial biomass formation was estimated to be 11 μg S g–1 soil and 21 μg S g–1 soil for glucose- and cellulose-amended soil, respectively. The highest levels of activity of the microbial biomass were observed at the SO4 2–-S concentrations of 14 μg S g–1 soil and 17 μg S g–1 soil, for the glucose and cellulose amendments, respectively, and were approximately 31–54% higher during glucose than cellulose decomposition.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 69 (1984), S. 199-204 
    ISSN: 1432-2242
    Keywords: Nicotiana rustica ; Temperature-pretreatment ; Anther culture ; Haploids ; Dihaploids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The efficiency of dihaploid production from anther culture in N. rustica has been improved by studying the effects of pretreatment temperature, pretreatment duration and initial anther stage on anther response, anther productivity and time to first plantlet production. Pretreatment was most effective on anthers at or around the stage of pollen mitosis. Pollen mitosis stage anthers pretreated at 9 °C for 15 days gave the best results. Both spontaneous and induced dihaploids were obtained. Small plantlets treated with 0.4% colchicine and 2% DMS solution for 5 h produced the maximum number of dihaploids (more than 50%). These considerable improvements in the efficiency of the techniques have made dihaploidy an attractive method for producing inbred lines in N. rustica. This will permit a large scale comparison of dihaploids with more conventional methods of inbreeding such as single seed descent and pedigree breeding.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 70 (1985), S. 128-132 
    ISSN: 1432-2242
    Keywords: Anther culture ; Androgenesis ; Haploid production ; Pretreatment ; Tobacco
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary A total of six genotypes of Nicotiana rustica comprising the two F1's (V2 × V12 and V1 × V5) and their parents were evaluated for their efficiency in haploid production. Excised immature flower buds with pollen at late uninucleate to early binucleate stage were pretreated for 21 days at 5 ° or 7 °C, or for 15 days at 9 °C before culturing on Nitsch's medium+ 0.1 mg/l NAA. The effects of genotype, pretreatment and their interaction were tested on anther response, anther productivity and days to first plantlet formation. Highly significant genotype X pretreatment interaction and differences between genotypes were observed for all three characters. Significant differences between pretreatments were observed for anther productivity only. The performance of V12 both in respect of anther productivity and response was highest whereas that of V5 was the lowest. Analysis of variance showed that a simple additive genetic model was not adequate to explain the above variation due to significant additive genetic and dominance interactions with the pretreatment.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    World journal of microbiology and biotechnology 10 (1994), S. 568-571 
    ISSN: 1573-0972
    Keywords: Cholera toxin ; non-culturable ; PCR ; Vibrio cholerae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Cholera enterotoxin is a major antigenic determinant for virulence of Vibrio cholerae O1 which can enter into a viable but non-culturable (N-C) state, not detectable by conventional culture methods, yet remain capable of producing enterotoxin and potentially pathogenic. PCR was applied in the current study to detect the chilera toxin (ctx) gene of N-C cells, thus eliminating the necessity of culture. Sets of oligonucleotide primers were designed, based on the ctxAB operon of V. cholerae O1, to detect the presence of the ctx gene. DNA from both culturable and N-C cells of V. cholerae O1 was amplified by PCR using sets of primers flanking 302-, 564- and 777-bp fragments of the ctx gene. The PCR method employed was capable of detecting the ctx gene in N-C V. cholerae in aquatic microcosms and in diarrheal stool samples from three patients who had distinct clinical symptoms of cholera but were culture-negative for V. cholerae O1 and non-O1 and enterotoxigenic Escherichia coli. Forty cycles of a two-step reaction (30 s each at 94 and 60°C) were optimal and more time efficient than a three-step PCR described previously. The procedure, from the point of heating microcosms or broth culture samples to observation on gels, requires 〈 4 h to complete.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1573-0972
    Keywords: Cholera toxin ; PCR ; Vibrio cholerae non-O1 ; V. cholerae O1 ; V. cholerae O139 ; Zonula occludens toxin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Vibrio cholerae O1 and V. cholerae non-O1 strains isolated from environmental samples collected in São Paulo, Brazil, during cholera epidemics and pre-epidemic periods were examined for the presence of toxin genes. V. cholerae O1 strains isolated from clinical samples in Peru and Mexico, and V. cholerae O139 strains from India were also examined for the presence of ctx (cholera toxin gene) and zot (zonula occludens toxin gene) by polymerase chain reaction (PCR). A modified DNA-extraction method applied in this study yielded satisfactory recovery of genomic DNA from vibrios. Results showed that strains of V. cholerae O1 isolated during the preepidemic period were ctx -/zot - whereas strains isolated during the epidemic were ctx +/zot +. All V. cholerae non-O1 strains tested in the study were ctx -/zot -, whereas all V. cholerae O139 strains were ctx +/zot +. Rapid detection of the virulence genes (ctx and zot) can be achieved by PCR and this can serve as an important tool in the epidemiology and surveillance of V. cholerae.
    Type of Medium: Electronic Resource
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