Soberon M, Lopez O, Morera C, Girard ML, Tabche ML, Miranda J
Departamento de Biologia Molecular de Plantas, Instituto de Biotecnologia, Universidad Nacional Autonoma de Mexico, Cuernavaca, Morelos 62271, Mexico.
Appl Environ Microbiol. 1999 May;65(5):2015-9. doi: 10.1128/AEM.65.5.2015-2019.1999.
The ntrC gene codes for a transcriptional activator protein that modulates gene expression in response to nitrogen. The cytochrome production pattern of a Rhizobium etli ntrC mutant (CFN2012) was studied. CO difference spectral analysis of membranes showed that CFN2012 produced a terminal oxidase similar to the symbiotic terminal oxidase of bacteroids in free-living cells under aerobic conditions, with a characteristic trough at 553 nm. CFN2012 produced two c-type cytochromes with molecular masses of 27 and 32 kDa, in contrast with the wild-type strain, which produced only a 32-kDa c-type cytochrome. The expression levels of the R. etli fixNOQP operon, which codes for terminal oxidase cbb3, were not affected by the ntrC mutation. However, the production levels of the two c-type cytochromes (27 and 32 kDa) were enhanced at least eightfold when the Bradyrhizobium japonicum fixNOQP operon was expressed in CFN2012 from the nptII promoter (pMSfixc), suggesting that these proteins are subunits FixO (27 kDa) and FixP (32 kDa) of cbb3 and that CFN2012/pMSfixc overproduced this terminal oxidase. CFN2012/pMSfixc showed a significant increase in its symbiotic performance as judged by the determination of nitrogenase activities of plants inoculated with this strain, suggesting that the overproduction of cbb3 terminal oxidase correlates with an enhancement in symbiotic nitrogen fixation.
ntrC基因编码一种转录激活蛋白,该蛋白可响应氮元素调节基因表达。对根瘤菌(Rhizobium etli)ntrC突变体(CFN2012)的细胞色素产生模式进行了研究。对细胞膜的一氧化碳差光谱分析表明,CFN2012在有氧条件下的自由生活细胞中产生一种类似于类菌体共生末端氧化酶的末端氧化酶,在553nm处有一个特征性低谷。与野生型菌株相比,CFN2012产生了两种分子量分别为27kDa和32kDa的c型细胞色素,而野生型菌株只产生一种32kDa的c型细胞色素。编码末端氧化酶cbb3的根瘤菌fixNOQP操纵子的表达水平不受ntrC突变的影响。然而,当来自nptII启动子(pMSfixc)的日本慢生根瘤菌(Bradyrhizobium japonicum)fixNOQP操纵子在CFN2012中表达时,这两种c型细胞色素(27kDa和32kDa)的产生水平至少提高了八倍,这表明这些蛋白质是cbb3的亚基FixO(27kDa)和FixP(32kDa),并且CFN2012/pMSfixc过量产生了这种末端氧化酶。通过测定接种该菌株的植物的固氮酶活性判断发现,CFN2012/pMSfixc的共生性能显著提高,这表明cbb3末端氧化酶的过量产生与共生固氮的增强相关。