首页> 外文OA文献 >Roles of SpoT and FNR in NH4+ assimilation and osmoregulation in GOGAT (glutamate synthase)-deficient mutants of Escherichia coli.
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Roles of SpoT and FNR in NH4+ assimilation and osmoregulation in GOGAT (glutamate synthase)-deficient mutants of Escherichia coli.

机译:SpoT和FNR在大肠杆菌GOGAT(谷氨酸合酶)缺陷型突变体中NH4 +同化和渗透调节中的作用。

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摘要

An osmosensitive mutant of Escherichia coli was isolated and shown to harbor two mutations that were together necessary for osmosensitivity. One (ossB) was an insertion mutation in the gltBD operon, which encodes the enzyme glutamate synthase (GOGAT), involved in ammonia assimilation and L-glutamate biosynthesis. The other (ossA) was in the fnr gene, encoding the regulator protein FNR for anaerobic gene expression. Several missense or deletion mutations in fnr and gltBD behaved like ossA and ossB, respectively, in conferring osmosensitivity. A mutation affecting the DNA-binding domain of FNR was recessive to fnr+ with respect to the osmotolerance phenotype but was dominant-negative for its effect on expression of genes in anaerobic respiration. Our results may most simply be interpreted as suggesting the requirement for monomeric FNR during aerobic growth of E. coli in high-osmolarity media, presumably for L-glutamate accumulation via the GOGAT-independent pathway (catalyzed by glutamate dehydrogenase [GDH]), but the mechanism of FNR action is not known. We also found that the spoT gene (encoding guanosine 3',5'-bispyrophosphate [ppGpp] synthetase II/ppGpp-3' pyrophosphohydrolase), in multiple copies, overcomes the defect in NH4+ assimilation associated with GOGAT deficiency and thereby suppresses osmosensitivity in gltBD fnr strains. Enhancement of GDH activity in these derivatives appears to be responsible for the observed suppression. Its likely physiological relevance was established by the demonstration that growth of gltBD mutants (that are haploid for spoT+) on moderately low [NH4+] was restored with the use of C sources poorer than glucose in the medium. Our results raise the possibility that SpoT-mediated accumulation of ppGpp during C-limited growth leads to GDH activation and that the latter enzyme plays an important role in N assimilation in situ hitherto unrecognized from studies on laboratory-grown cultures.
机译:分离了一种大肠杆菌的渗透敏感性突变体,并显示出具有两个对渗透敏感性而言都是必需的突变。一个(ossB)是gltBD操纵子中的插入突变,它编码谷氨酰胺合酶(GOGAT),参与氨同化和L-谷氨酸的生物合成。另一个(ossA)位于fnr基因中,编码用于厌氧基因表达的调节蛋白FNR。在赋予渗透压敏感性时,fnr和gltBD中的几个错义或缺失突变分别表现为ossA和ossB。影响FNR的DNA结合结构域的突变在渗透耐受表型方面对fnr +呈隐性,但对厌氧呼吸中基因表达的影响呈显性负性。我们的结果可能最简单地解释为,表明在高渗透压培养基中大肠杆菌有氧生长期间需要单体FNR,大概是通过GOGAT独立途径(由谷氨酸脱氢酶[GDH]催化)进行的L-谷氨酸积累,但是FNR作用的机制尚不清楚。我们还发现,spoT基因(编码鸟苷3',5'-双焦磷酸[ppGpp]合成酶II / ppGpp-3'焦磷酸水解酶)可以多份复制,克服了与GOGAT缺乏相关的NH4 +同化缺陷,从而抑制了gltBD的渗透敏感性fnr株。这些衍生物中GDH活性的增强似乎是所观察到的抑制的原因。通过证明在培养基中使用比葡萄糖弱的碳源,可以恢复gltBD突变体(对于spoT +是单倍体)在较低[NH4 +]上的生长,从而证实了其可能的生理相关性。我们的结果提出了这样的可能性,即C限制生长期间SpoT介导的ppGpp积累会导致GDH活化,而后者至今在实验室培养的研究中尚未被认识到,在原位N同化中起着重要作用。

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