Olson J W, Maier R J
Department of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Gene. 1997 Oct 15;199(1-2):93-9. doi: 10.1016/s0378-1119(97)00352-1.
A region of DNA 6 kb downstream of the hydrogenase (H2ase) structural genes and directly downstream of the hypB gene of Bradyrhizobium japonicum was shown by mutational analysis to be necessary for H2ase synthesis. Sequencing of this region revealed two complete open reading frames, and the 5' fragment of a third ORF. They encode proteins with homologies to the HypF, HypC and the N-terminus of HypD from other H2ase-containing organisms. The hypF of B. japonicum encodes a 753-aa protein with a predicted molecular mass of 80.3 kDa that contains the two zinc-finger motifs characteristic of other HypF proteins. The hypC encodes a 85-aa protein with a predicted molecular mass of 8.4 kDa. The 5' portion of hypD, which encodes the first 35 aa, upon combining with the previously reported C-terminus of HypD, designated HypD' (Van Soom et al. (1993) Mol. Gen. Genet. 239, 235-240) encodes a protein with a predicted molecular mass of 42.4 kDa. Complementation studies on a H2 uptake defective strain of B. japonicum containing a polar mutation in the hyp operon revealed that the products of the hyp F, C, D, E genes are required for H2ase production. Evidence is also presented that the hyp genes are co-transcribed from a large operon together with the downstream genes hupGHIJK, making a polycistronic message of 11 genes.
通过突变分析表明,日本慢生根瘤菌氢化酶(H2ase)结构基因下游6 kb且直接位于hypB基因下游的一段DNA区域是H2ase合成所必需的。对该区域进行测序发现了两个完整的开放阅读框以及第三个开放阅读框的5'端片段。它们编码的蛋白质与其他含H2ase的生物体中的HypF、HypC和HypD的N端具有同源性。日本慢生根瘤菌的hypF编码一个753个氨基酸的蛋白质,预测分子量为80.3 kDa,该蛋白质含有其他HypF蛋白特有的两个锌指基序。hypC编码一个85个氨基酸的蛋白质,预测分子量为8.4 kDa。hypD的5'部分编码前35个氨基酸,与先前报道的HypD的C端(称为HypD',Van Soom等人(1993年)《分子与普通遗传学》239卷,235 - 240页)结合后,编码一个预测分子量为42.4 kDa的蛋白质。对含有hyp操纵子极性突变的日本慢生根瘤菌H2吸收缺陷菌株进行的互补研究表明,hyp F、C、D、E基因的产物是H2ase产生所必需的。同时也有证据表明,hyp基因与下游基因hupGHIJK一起从一个大操纵子中共同转录,形成一个包含11个基因的多顺反子信息。