By A.H. Rose and J. Gareth Morris (Eds.)
This quantity in a research-level sequence covers assorted features 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 cellphone partitions. it's meant to be of use to microbiologists, biochemists and biotechnologists. different similar works during this sequence are volumes 29, 30 and 31.
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The papers assembled during this assortment contain a majority of the oral displays in addition to a number of poster shows given on the twenty second Annual Symposium prepared by way of the Bastern Pennsylvania department of the yank Society for MicrobioloS)'. The symposium wouldn't be attainable with no the beneficiant aid of the various sponsors (see sponsor checklist) or with no the concerted attempt of a11 the Committee contributors.
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Extra info for Advances in Microbial Physiology, Vol. 21
P. Journalof GeneralMicrobiology 25, 47. Daniel, J. , Sievert, A. H. and Rusch, H . P. JournalofBacteriology 86, 324. Davies, K. E. and Walker, I. 0. Journalof CellScience 26, 267. Davies, K. E. and Walker, I. 0. (1978). Federation of European Biochemical Societies Letters 86,303. Dee, J. (1975). Science Progress 62, 523. , Sentenac, A. and Fromageot, P. (1976). European Journal of Biochemistry 65,543. Dove, W. F. and Rusch, H. P. (1979). ” Princeton University Press, in press. Ernst, G. H. and Sauer, H.
1979) but direct evidence has not yet been reported and might, in fact, be rather difficult to obtain at present. 2 . Regulatory Factors A third alternative, the presence of regulatory factors of various kinds, is amenable to analysis and evidence for several such factors has been reported. B). , 1969b1, although this possibility still remains to be explored. , 1979). Here again, no information is yet available o n its actual role in the regulation of transcription during the cell cycle. E) has been correlated with transcriptional activity during the cell cycle in vivo.
1966; Zellweger and Braun, 197 1 ; see Section 111). A more detailed investigation of the basic requirements and the action of several transcription inhibitors suggested the existence of at least two different RNA polymerases in nuclei before these enzymes were actually isolated and characterized biochemically (Grant, 1972). Isolated nucleoli were shown to contain an RNA polymerase activity which was largely resistant to the fungal toxin a-amanitin. This enzyme TRANSCRIPTION IN ACELLUIAR SLIME MOULDS 21 was minimally active at 10 mM MgCI, and under low salt conditions, and no additional stimulation could be achieved by the addition of Mn2+or by raising the ionic strength of the incubation medium.
Advances in Microbial Physiology, Vol. 21 by A.H. Rose and J. Gareth Morris (Eds.)