Download e-book for iPad: Advances in Microbial Physiology, Vol. 28 by A.H. Rose, D.W. Tempest (Eds.)

By A.H. Rose, D.W. Tempest (Eds.)

ISBN-10: 012027728X

ISBN-13: 9780120277285

This quantity in a research-level sequence covers different facets of microbial body structure and biochemistry together with inositol metabolisms in yeasts, bacterial adhesion, natural acids, the bacterial flagellum and the mechanical behaviour of bacterial mobilephone partitions. it's meant to be of use to microbiologists, biochemists and biotechnologists. different comparable works during this sequence are volumes 29, 30 and 31.

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Extra resources for Advances in Microbial Physiology, Vol. 28

Example text

In both mutant strains the basal concentration of the 56,000 molecular-weight protein, prior to heat induction, was very high in comparison with the concentration in the wild type. The B. frugilis heat-resistant mutants are interesting in that both mutants, which were isolated from different mutation experiments, had lost the ability to synthesize the same two proteins after heat treatment. These two proteins are synthesized by the wild type after exposure to heat. This suggests that the proteins with apparent molecular weights of 125,000 and 52,000 are not involved in heat resistance in B.

The apparent molecular weights of the heat-shock proteins in B. fragilis differed from those observed in E. , 1984). In E. fragilis. Heat and ethanol stress did not induce phage reactivation. Both chemical and environmental stresses have been shown to induce the heat-shock proteins in a number of organisms (Ashburner and Bonner, 1979). , 1984). Because 0 2 and H202 are likely to be natural stresses for anaerobic bacteria, it is not unreasonable to expect that similar proteins would be induced by heat, 0 2 and H202.

The sporulation developmental stages occurred near-synchronously rendering the system amenable to correlative morphological and biochemical studies. , 1977). , 1982). A chemically defined minimal medium which allowed both the production of significant concentrations of solvents and high levels of sporulation in an industrial strain of C. acetobutylicum (strain P262), was described by Long et al. (1983). The developmental sequence was sufficiently synchronous in this medium to enable the system to be used for correlative physiological and biochemical studies.

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Advances in Microbial Physiology, Vol. 28 by A.H. Rose, D.W. Tempest (Eds.)


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