By A.H. Rose, D.W. Tempest (Eds.)
This quantity in a research-level sequence covers assorted points 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 telephone partitions. it truly is 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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Additional info for Advances in Microbial Physiology, Vol. 28
1979). Bacteroidesfragilis is another bacterium that also appears to differ since it is a non-competent strain and appears to lack an error-prone system. I. REPAIR-DEFICIENT MUTANTS Although it has been stressed that the isolation of mutants of B. fragilis is difficult, nevertheless it is important that mutants are obtained and characterized. The use of mutants has been instrumental in accelerating the progress of research on DNA repair systems in E. coli. After an extensivesearch, Abratt et al.
Frugilis. Both mutants also showed a high constitutive level of a protein with an apparent molecular weight of approximately 56,000 which is an inducible heat-shock protein in the wildtype strain. The high concentrations of this protein in the mutant cells prior to heat treatment may contribute to the heat resistance of the mutants. 24 D. R. WOODS AND D. T. JONES H. ERROR-FREE REPAIR IN Bacteroides fragilis Some major conclusions can now be drawn on the responses of B. fragilis to DNA-damaging agents.
Fragilis may not have a typical E. coli red-type mediated response. fragilis cells and phage mutagenesis after treatment with DNA-damaging agents; (ii) a protein with a molecular weight of 37,000 to 40,000 is not induced by UV radiation in B. fragilis; (iii) the response of B. fragilis cells to LHR and near-UV radiation resembles that of E. coli recA mutants, and (iv) extensive DNA degradation after UV radiation occurs in B. fragilis and E. coli r e d mutant cells. If the absence of an errorprone system is confirmed in B.
Advances in Microbial Physiology, Vol. 28 by A.H. Rose, D.W. Tempest (Eds.)