Marietou Angeliki, Richardson David, Cole Jeff, Mohan Sudesh
School of Biosciences, University of Birmingham, Birmingham B15 2TT, UK.
FEMS Microbiol Lett. 2005 Jul 15;248(2):217-25. doi: 10.1016/j.femsle.2005.05.042.
Many sulphate reducing bacteria can also reduce nitrite, but relatively few isolates are known to reduce nitrate. Although nitrate reductase genes are absent from Desulfovibrio vulgaris strain Hildenborough, for which the complete genome sequence has been reported, a single subunit periplasmic nitrate reductase, NapA, was purified from Desulfovibrio desulfuricans strain 27774, and the structural gene was cloned and sequenced. Chromosome walking methods have now been used to determine the complete sequence of the nap gene cluster from this organism. The data confirm the absence of a napB homologue, but reveal a novel six-gene organisation, napC-napM-napA-napD-napG-napH. The NapC polypeptide is more similar to the NrfH subgroup of tetraheme cytochromes than to NapC from other bacteria. NapM is predicted to be a tetra-heme c-type cytochrome with similarity to the small tetraheme cytochromes from Shewanella oneidensis. The operon is located close to a gene encoding a lysyl-tRNA synthetase that is also found in D. vulgaris. We suggest that electrons might be transferred to NapA either from menaquinol via NapC, or from other electron donors such as formate or hydrogen via the small tetraheme cytochrome, NapM. We also suggest that, despite the absence of a twin-arginine targeting sequence, NapG might be located in the periplasm where it would provide an alternative direct electron donor to NapA.
许多硫酸盐还原菌也能还原亚硝酸盐,但已知能还原硝酸盐的分离菌株相对较少。尽管已报道了完整基因组序列的希登伯勒脱硫弧菌菌株中不存在硝酸盐还原酶基因,但从脱硫脱硫弧菌菌株27774中纯化出了一种单亚基周质硝酸盐还原酶NapA,并对其结构基因进行了克隆和测序。现在已使用染色体步移法来确定该生物体nap基因簇的完整序列。数据证实不存在napB同源物,但揭示了一种新的六基因组织,即napC-napM-napA-napD-napG-napH。NapC多肽与四血红素细胞色素的NrfH亚组比与其他细菌的NapC更相似。预测NapM是一种四血红素c型细胞色素,与来自奥奈达希瓦氏菌的小四血红素细胞色素相似。该操纵子位于一个编码赖氨酰-tRNA合成酶的基因附近,该基因在希登伯勒脱硫弧菌中也有发现。我们认为电子可能通过NapC从甲基萘醌转移到NapA,或者通过小四血红素细胞色素NapM从其他电子供体如甲酸或氢气转移到NapA。我们还认为,尽管不存在双精氨酸靶向序列,但NapG可能位于周质中,在那里它将为NapA提供另一种直接电子供体。