Biomedical subjects
H D Singh
Publications and source records attributed to H D Singh.
Metabolic blocks in the degradation of beta-sitosterol by a plasmid-cured strain of Arthrobacter oxydans.
Plasmid-harbouring, sterol-decomposing organism Arthrobacter oxydans 317 was treated with sodium dodecylsulphate to obtain a plasmid-cured strain A. oxydans 317 A1 incapable of utilizing 4-androstene-3,17-dione (AD). The strain 317 A1 was unable to degrade beta-sitosterol side chain completely to form AD but could carry out partial degradation as shown by the accumulation of 3-oxochol-4-en-24-oic acid as a major metabolite and 27-norcholest-4-en-3,24-dione as a minor metabolite. The strain could form 1,4-androstadiene-3,17-dione (ADD) from 3-oxo-23,24-bisnorchol-1,4-dien-22- oic acid (BNC) to a limited extent. The existence of metabolic blocks in the conversion of 3-oxochol-4-en-24-oic acid to 3-oxo-23,24-bis-norchol-4-en-22-oic acid and further conversion to AD by the plasmid-cured strain 317 A1 was suggested. Neither the formation of ADD from AD nor the conversion of AD and ADD to 9 alpha-hydroxy derivatives leading to steroid ring opening could be done by the plasmid-cured strain but the 17 beta-reduction of AD and ADD and 1(2)-reduction of ADD were not affected by the absence of the plasmid. It was proposed that plasmid determines 1(2)-dehydrogenation and 9 alpha-hydroxylation of steroid ring structure in this organism.
Factors limiting the microbial conversion of sterols to 17-ketosteroids in the presence of metal chelate inhibitors.
Bioconversion of sterols to 17-ketosteroids by an Arthrobacter species occurred in the presence of hydrophobic metal-chelating agents but the production of 17-ketosteroids (17-KS) was seriously limited by the rapid loss of the viability of cells in the presence of these inhibitors. Besides, the conversion was inhibited by 17-KS at concentrations of 500 ppm or more. The 17-KS formed consisted exclusively of 1,4-androstadiene-3,17-dione (ADD) and 4-androstene-3,17-dione (AD) and these were found in the extracellular medium predominantly in bound form or as molecular aggregates which may limit their accumulation. It was concluded that enhanced production of 17-KS could be achieved by protecting the viability of cells and by removing the steroid metabolites from the site of inhibition.
Isolation and characterisation of sterol metabolites formed by an Arthrobacter species.
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Peak expiratory flow rates in South Indian children and adolescents.
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Metabolism of n-alkane in Endomycopsis lipolytica (Saccharomycopsis lipolytica): Part IV--Characteristics of lipid formation from n-alkanes by non-proliferating cells.
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A study of menarcheal age in India.
A study of menarcheal age was carried out in southern India. A logit method of analysis was applied to status quo data on 1267 Tamil and Telugu speaking girls aged 9 to 18 years in 3 schools catering for different socio-economic groups. There appears to be no relationship of menarcheal age with dietary pattern classified simply as vegetarian and non-vegetarian. Differences in median age at menarche between schools correspond well with the socio-economic differences between them. The median age in the most advantaged school (12-86 years) is comparable with that in recent studies in southern and eastern Europe, and may perhaps be in advance of some recent north-west European samples.
Expiratory flow rates in boys.
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Letter: Menarcheal age in South India.
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Formation of salicylic acid from naphthalene by microorganisms: Part I. Studies on isolation, characterization & growth of bacterial isolates utilizing naphthalene.
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Formation of salicylic acid from naphthalene by microorganisms: Part II. Factors affecting salicylic acid accumulation.
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Metabolism of n-alkane in Endomycopsis lipolytica (Saccharomycopsis lipolytica): Part III. Formation of carbohydrates from hydrocarbons.
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Microbial biomass production of solid hydrocarbons.
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Growth characteristics of the strains of Saccharomycopsis lipolytica on hydrocarbons.
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Family size and age of menarche.
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Measurement of flow rates over the third quarter and middle litre of maximal forced expiration as indices of ventilatory function.
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Ascospore formation in yeasts during active growth on hydrocarbons.
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Simple method for inducing ascospore formation in yeasts.
A new method for inducing ascospore formation in yeasts is described and compared with conventional methods for its performance. The method has the advantage of simplicity, reproducibility, and saving of time.