Nicoloff Hervé, Arsène-Ploetze Florence, Malandain Cédric, Kleerebezem Michiel, Bringel Françoise
Laboratoire de Dynamique, Evolution et Expression de Génomes de Microorganismes, Université Louis Pasteur/CNRS FRE 2326, 28 rue Goethe, 67083 Strasbourg, France.
J Bacteriol. 2004 Sep;186(18):6059-69. doi: 10.1128/JB.186.18.6059-6069.2004.
The repression of the carAB operon encoding carbamoyl phosphate synthase leads to Lactobacillus plantarum FB331 growth inhibition in the presence of arginine. This phenotype was used in a positive screening to select spontaneous mutants deregulated in the arginine biosynthesis pathway. Fourteen mutants were genetically characterized for constitutive arginine production. Mutations were located either in one of the arginine repressor genes (argR1 or argR2) present in L. plantarum or in a putative ARG operator in the intergenic region of the bipolar carAB-argCJBDF operons involved in arginine biosynthesis. Although the presence of two ArgR regulators is commonly found in gram-positive bacteria, only single arginine repressors have so far been well studied in Escherichia coli or Bacillus subtilis. In L. plantarum, arginine repression was abolished when ArgR1 or ArgR2 was mutated in the DNA binding domain, or in the oligomerization domain or when an A123D mutation occurred in ArgR1. A123, equivalent to the conserved residue A124 in E. coli ArgR involved in arginine binding, was different in the wild-type ArgR2. Thus, corepressor binding sites may be different in ArgR1 and ArgR2, which have only 35% identical residues. Other mutants harbored wild-type argR genes, and 20 mutants have lost their ability to grow in normal air without carbon dioxide enrichment; this revealed a link between arginine biosynthesis and a still-unknown CO2-dependent metabolic pathway. In many gram-positive bacteria, the expression and interaction of different ArgR-like proteins may imply a complex regulatory network in response to environmental stimuli.
编码氨甲酰磷酸合成酶的carAB操纵子的抑制会导致植物乳杆菌FB331在精氨酸存在的情况下生长受到抑制。这种表型被用于阳性筛选,以选择在精氨酸生物合成途径中失调的自发突变体。对14个突变体进行了组成型精氨酸产生的遗传特征分析。突变位于植物乳杆菌中存在的精氨酸阻遏基因之一(argR1或argR2)中,或位于参与精氨酸生物合成的双极carAB-argCJBDF操纵子基因间区域的假定ARG操纵子中。尽管在革兰氏阳性细菌中通常发现有两个ArgR调节因子,但到目前为止,在大肠杆菌或枯草芽孢杆菌中仅对单个精氨酸阻遏因子进行了深入研究。在植物乳杆菌中,当ArgR1或ArgR2在DNA结合结构域、寡聚化结构域发生突变,或者ArgR1中发生A123D突变时,精氨酸阻遏作用就会被消除。与大肠杆菌ArgR中参与精氨酸结合的保守残基A124等效的A123,在野生型ArgR2中是不同的。因此,辅阻遏物结合位点在ArgR1和ArgR2中可能不同,它们只有35%的相同残基。其他突变体含有野生型argR基因,并且有20个突变体在没有二氧化碳富集的正常空气中失去了生长能力;这揭示了精氨酸生物合成与一个仍未知的二氧化碳依赖代谢途径之间的联系。在许多革兰氏阳性细菌中,不同ArgR样蛋白的表达和相互作用可能意味着存在一个响应环境刺激的复杂调控网络。