Myers C R, Myers J M
Department of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee 53226, USA.
J Bacteriol. 1997 Feb;179(4):1143-52. doi: 10.1128/jb.179.4.1143-1152.1997.
The cymA gene, which encodes a tetraheme cytochrome c, was cloned from Shewanella putrefaciens MR-1. This gene complemented a mutant which had a TnphoA insertion in cymA and which was deficient in the respiratory reduction of iron(III), nitrate, fumarate, and manganese(IV). The 561-bp nucleotide sequence of cymA encodes a protein of 187 amino acids with a predicted molecular mass of 20.8 kDa. No N-terminal signal sequence was readily apparent; consistent with this, a cytochrome with a size of 21 kDa was detected in the wild type but was absent in the insertional mutant. The cymA gene is transcribed into an mRNA; the major transcript was approximately 790 bases, suggesting that it is not part of a multicistronic operon. This RNA transcript was not detected in the cymA mutant. The CymA protein was found in the cytoplasmic membrane and soluble fraction of MR-1, and it shares partial amino acid sequence homology with multiheme c-type cytochromes from other bacteria. These cytochromes are ostensibly involved in the transfer of electrons from the cytoplasmic membrane to acceptors in the periplasm. The localization of the fumarate and iron(III) reductases to the periplasm and outer membrane of MR-1, respectively, suggests the possibility of a similar electron transfer role for CymA.
编码四血红素细胞色素c的cymA基因是从腐败希瓦氏菌MR-1中克隆得到的。该基因对一个在cymA中发生TnphoA插入且在铁(III)、硝酸盐、富马酸盐和锰(IV)的呼吸还原方面存在缺陷的突变体起到了互补作用。cymA的561个碱基对的核苷酸序列编码了一个由187个氨基酸组成的蛋白质,预测分子量为20.8 kDa。未明显发现N端信号序列;与此一致的是,在野生型中检测到了大小为21 kDa的细胞色素,但在插入突变体中未检测到。cymA基因转录成一种mRNA;主要转录本约为790个碱基,这表明它不是多顺反子操纵子的一部分。在cymA突变体中未检测到这种RNA转录本。CymA蛋白存在于MR-1的细胞质膜和可溶性部分中,并且它与来自其他细菌的多血红素c型细胞色素具有部分氨基酸序列同源性。这些细胞色素表面上参与了电子从细胞质膜向周质中的受体转移。富马酸盐还原酶和铁(III)还原酶分别定位于MR-1的周质和外膜,这表明CymA可能具有类似的电子转移作用。