Durmowicz M C, Maier R J
Department of Biology, Johns Hopkins University, Baltimore, Maryland 21218, USA.
J Bacteriol. 1998 Jun;180(12):3253-6. doi: 10.1128/JB.180.12.3253-3256.1998.
The roles of the nitrogen fixation regulatory proteins NifA, FixK1, and FixK2 in the symbiotic regulation of hydrogenase structural gene expression in Bradyrhizobium japonicum have been investigated. Bacteroids from FixJ and FixK2 mutants have little or no hydrogenase activity, and extracts from these mutant bacteroids contain no hydrogenase protein. Bacteroids from a FixK1 mutant exhibit wild-type levels of hydrogenase activity. In beta-galactosidase transcriptional assays with NifA and FixK2 expression plasmids, the FixK2 protein induces transcription from the hup promoter to levels similar to those induced by HoxA, the transcriptional activator of free-living hydrogenase expression. The NifA protein does not activate transcription at the hydrogenase promoter. Therefore, FixK2 is involved in the transcriptional activation of symbiotic hydrogenase expression. By using beta-galactosidase transcriptional fusion constructs containing successive truncations of the hup promoter, the region of the hup promoter required for regulation by FixK2 was determined to be between 29 and 44 bp upstream of the transcription start site.
对慢生根瘤菌中固氮调节蛋白NifA、FixK1和FixK2在氢化酶结构基因表达共生调节中的作用进行了研究。来自FixJ和FixK2突变体的类菌体几乎没有或没有氢化酶活性,并且这些突变类菌体的提取物中不含氢化酶蛋白。来自FixK1突变体的类菌体表现出野生型水平的氢化酶活性。在用NifA和FixK2表达质粒进行的β-半乳糖苷酶转录分析中,FixK2蛋白诱导hup启动子的转录至与自由生活氢化酶表达的转录激活因子HoxA诱导的水平相似。NifA蛋白不会在氢化酶启动子处激活转录。因此,FixK2参与共生氢化酶表达的转录激活。通过使用包含hup启动子连续截短的β-半乳糖苷酶转录融合构建体,确定FixK2调节所需的hup启动子区域位于转录起始位点上游29至44 bp之间。