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参与硫酸盐活化的苜蓿根瘤菌基因:nodPQ的两个拷贝和一个新位点saa。

Rhizobium meliloti genes involved in sulfate activation: the two copies of nodPQ and a new locus, saa.

作者信息

Schwedock J S, Long S R

机构信息

Department of Biological Sciences, Stanford University, California 94305-5020.

出版信息

Genetics. 1992 Dec;132(4):899-909. doi: 10.1093/genetics/132.4.899.

Abstract

The nitrogen-fixing symbiont Rhizobium meliloti establishes nodules on leguminous host plants. Nodulation (nod) genes used for this process are located in a cluster on the pSym-a megaplasmid of R. meliloti. These genes include nodP and nodQ (here termed nodPQ), which encode ATP sulfurylase and APS kinase, enzymes that catalyze the conversion of ATP and SO(4)2- into the activated sulfate form 3'-phosphoadenosine 5'-phosphosulfate (PAPS), an intermediate in cysteine synthesis. In Rhizobium, PAPS is also a precursor for sulfated and N-acylated oligosaccharide Nod-factor signals that cause symbiotic responses on specific host plants such as alfalfa. We previously found a highly conserved second copy of nodPQ in R. meliloti. We report here the mapping and cloning of this second copy, and its location on the second megaplasmid, pSym-b. The function of nodP2Q2 is equivalent to that of nodP1Q1 in complementation tests of R. meliloti and Escherichia coli mutants in ATP sulfurylase and adenosine 5'-phosphosulfate (APS) kinase. Mutations in nodP2Q2 do not have as severe an effect on symbiosis or plant host range as do those in nodP1Q1, however, possibly reflecting differences in expression and/or channeling of metabolites to specific enzymes involved in sulfate transfer. Strains mutated or deleted for both copies of nodQ are severely defective in symbiotic phenotypes, but remain prototrophic. This suggests the existence in R. meliloti of a third locus for ATP sulfurylase and APS kinase activities. We have found a new locus saa (sulfur amino acid), which may also encode these activities.

摘要

固氮共生菌苜蓿根瘤菌在豆科宿主植物上形成根瘤。用于此过程的结瘤(nod)基因位于苜蓿根瘤菌的pSym-a大质粒上的一个簇中。这些基因包括nodP和nodQ(此处称为nodPQ),它们编码ATP硫酸化酶和APS激酶,这些酶催化ATP和SO₄²⁻转化为活化的硫酸盐形式3'-磷酸腺苷5'-磷酸硫酸酯(PAPS),这是半胱氨酸合成中的一种中间体。在根瘤菌中,PAPS也是硫酸化和N-酰化寡糖Nod因子信号的前体,这些信号会在特定宿主植物如苜蓿上引发共生反应。我们之前在苜蓿根瘤菌中发现了nodPQ的一个高度保守的第二拷贝。我们在此报告该第二拷贝的定位和克隆,以及它在第二个大质粒pSym-b上的位置。在苜蓿根瘤菌和大肠杆菌突变体的ATP硫酸化酶和腺苷5'-磷酸硫酸酯(APS)激酶互补试验中,nodP2Q2的功能与nodP1Q1的功能相当。然而,nodP2Q2中的突变对共生或植物宿主范围的影响不如nodP1Q1中的突变那么严重,这可能反映了代谢物向参与硫酸盐转移的特定酶的表达和/或输送方面的差异。两个nodQ拷贝都发生突变或缺失的菌株在共生表型上存在严重缺陷,但仍为原养型。这表明苜蓿根瘤菌中存在第三个ATP硫酸化酶和APS激酶活性位点。我们发现了一个新的位点saa(硫氨基酸),它也可能编码这些活性。

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