首页> 美国卫生研究院文献>Journal of Bacteriology >Posttranslational regulation of nitrogenase in Rhodospirillum rubrum strains overexpressing the regulatory enzymes dinitrogenase reductase ADP-ribosyltransferase and dinitrogenase reductase activating glycohydrolase.
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Posttranslational regulation of nitrogenase in Rhodospirillum rubrum strains overexpressing the regulatory enzymes dinitrogenase reductase ADP-ribosyltransferase and dinitrogenase reductase activating glycohydrolase.

机译:翻译翻译:红曲霉菌株中过氧化氮酶的翻译后调控过表达调控酶二氮酶还原酶ADP-核糖基转移酶和二氮酶还原酶激活糖水解酶。

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摘要

Rhodospirillum rubrum strains that overexpress the enzymes involved in posttranslational nitrogenase regulation, dinitrogenase reductase ADP-ribosyltransferase (DRAT) and dinitrogenase reductase activating glycohydrolase (DRAG), were constructed, and the effect of this overexpression on in vivo DRAT and DRAG regulation was investigated. Broad-host-range plasmid constructs containing a fusion of the R. rubrum nifH promoter and translation initiation sequences to the second codon of draT, the first gene of the dra operon, were constructed. Overexpression plasmid constructs which overexpressed (i) only functional DRAT, (ii) only functional DRAG and presumably the putative downstream open reading frame (ORF)-encoded protein, or (iii) all three proteins were generated and introduced into wild-type R. rubrum. Overexpression of DRAT still allowed proper regulation of nitrogenase activity, with ADP-ribosylation of dinitrogenase reductase by DRAT occurring only upon dark or ammonium stimuli, suggesting that DRAT is still regulated upon overexpression. However, overexpression of DRAG and the downstream ORF altered nitrogenase regulation such that dinitrogenase reductase did not accumulate in the ADP-ribosylated form under inactivation conditions, suggesting that DRAG was constitutively active and that therefore DRAG regulation is altered upon overexpression. Proper DRAG regulation was observed in a strain overexpressing DRAT, DRAG, and the downstream ORF, suggesting that a proper balance of DRAT and DRAG levels is required for proper DRAG regulation.
机译:构建了过量表达翻译后固氮酶调控酶,双氮还原酶还原酶ADP-核糖基转移酶(DRAT)和双氮还原酶活化糖水解酶(DRAG)的红螺螺旋藻菌株,并研究了这种过表达对体内DRAT和DRAG调控的影响。构建了宽宿主范围的质粒构建体,该构建体包含了红曲霉nifH启动子和draT的第二个密码子(dra操纵子的第一个基因)的翻译起始序列的融合体。产生过表达(i)仅功能性DRAT,(ii)仅功能性DRAG和推测的下游开放阅读框(ORF)编码蛋白或(iii)所有这三种蛋白的过表达质粒构建体,并将其引入野生型R.红麻。 DRAT的过表达仍然允许适当调节固氮酶的活性,DRAT的ADP核糖基化二硝基酶还原酶仅在黑暗或铵刺激下发生,这表明DRAT在过表达时仍受调控。但是,DRAG的过表达和下游ORF改变了固氮酶的调节,以致在失活条件下二氮酶还原酶不会以ADP-核糖基化形式积累,这表明DRAG具有组成性活性,因此DRAG的调节在过表达时会发生改变。在过表达DRAT,DRAG和下游ORF的菌株中观察到适当的DRAG调节,这表明适当的DRAG调节需要DRAT和DRAG水平的适当平衡。

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