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氨基酸剥夺诱导λ样原噬菌体:差异诱导性;recA的作用。

Induction of lambdoid prophages by amino acid deprivation: differential inducibility; role of recA.

作者信息

Melechen N E, Go G

出版信息

Mol Gen Genet. 1980;180(1):147-55. doi: 10.1007/BF00267364.

Abstract

Lambda prophage in auxotrophic lysogens can be induced by omission of one or combinations of the required amino acids from the culture medium. Such amino acid deprivation can result in nearly as effective induction of lambda as thymine deprivation. Prophage 424 is also induced equally effectively under both conditions although to a lesser extent than lambda. By contrast prophage 21 and lambda i21 are differentially induced effectively by thymine deprivation and virtually not at all during amino acid deprivation. The same differential induction of 21 and equivalent induction of lambda and 424 occur when all three prophages are present in the same lysogen. Increasing the levels of lambda repressor with a cI carrying-plasmid prevented amino acidless induction of lambda as did the lambda ind- mutation. A recA, but not a recB, mutation in the host prevented induction by amino acid deprivation. A recC mutant host showed increased spontaneous induction of lambda and 21 prophages. The findings reported are used as an argument that the recA protease probably is not itself acting as the inducing protease and that a likely source of the observed specificity is an effector molecule. Different effector molecules may be produced in response to different exigent situations, to which the phage repressors may have evolved sensitivity. lambda i80 was inducible both by amino acid and thymine deprivation.

摘要

营养缺陷型溶原菌中的λ原噬菌体可通过从培养基中去除一种或多种所需氨基酸来诱导。这种氨基酸剥夺可导致几乎与胸腺嘧啶剥夺一样有效地诱导λ原噬菌体。原噬菌体424在这两种条件下也能被同样有效地诱导,尽管程度比λ原噬菌体小。相比之下,原噬菌体21和λi21在胸腺嘧啶剥夺时能被有效差异诱导,而在氨基酸剥夺时几乎完全不被诱导。当所有三种原噬菌体存在于同一溶原菌中时,21也会出现同样的差异诱导,而λ和424会出现同等诱导。用携带cI的质粒增加λ阻遏物的水平可阻止λ原噬菌体因无氨基酸而被诱导,λind-突变也有同样效果。宿主中的recA突变(而非recB突变)可阻止因氨基酸剥夺而产生的诱导。recC突变宿主显示出λ和21原噬菌体的自发诱导增加。所报道的这些发现被用作一种论据,即recA蛋白酶可能本身并不作为诱导蛋白酶起作用,而且观察到的特异性的一个可能来源是一种效应分子。可能会针对不同的紧急情况产生不同的效应分子,噬菌体阻遏物可能已经进化出对这些效应分子的敏感性。λi80可被氨基酸剥夺和胸腺嘧啶剥夺诱导。

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