Amar M, Patriarca E J, Manco G, Bernard P, Riccio A, Lamberti A, Defez R, Iaccarino M
International Institute of Genetics and Biophysics, Naples, Italy.
Mol Microbiol. 1994 Feb;11(4):685-93. doi: 10.1111/j.1365-2958.1994.tb00346.x.
We isolated a Rhizobium leguminosarum mutant strain altered in the glnB gene. This event, which has never been described in the Rhizobiaceae, is rare in comparison to mutants isolated in the contiguous gene, glnA. The glnB mutation removes the glnBA promoter but in vivo does not prevent glnA expression from its own promoter, which is not nitrogen regulated. The glnB mutant strain does not grow on nitrate as a sole nitrogen source and it is Nod+, Fix+. Two -24/-12 promoters, for the glnII and glnBA genes, are constitutively expressed in the glnB mutant, while two -35/-10-like promoters for glnA and ntrBC are unaffected. We propose that the glnB gene product, the PII protein, plays a negative role in the ability of NtrC to activate transcription from its target promoters and a positive role in the mechanism of nitrate utilization.
我们分离出了一株在glnB基因上发生改变的豌豆根瘤菌突变菌株。这一事件在根瘤菌科中从未被描述过,与在相邻基因glnA中分离出的突变体相比是罕见的。glnB突变去除了glnBA启动子,但在体内并不阻止glnA从其自身不受氮调控的启动子进行表达。glnB突变菌株不能以硝酸盐作为唯一氮源生长,并且它是结瘤阳性、固氮阳性。glnII和glnBA基因的两个-24/-12启动子在glnB突变体中组成型表达,而glnA和ntrBC的两个-35/-10样启动子不受影响。我们提出,glnB基因产物PII蛋白在NtrC激活其靶启动子转录的能力中起负作用,而在硝酸盐利用机制中起正作用。