Jamieson D J, Sawers R G, Rugman P A, Boxer D H, Higgins C F
J Bacteriol. 1986 Oct;168(1):405-11. doi: 10.1128/jb.168.1.405-411.1986.
Hydrogen metabolism in Salmonella typhimurium is differentially regulated by mutations in the two anaerobic regulatory pathways, defined by the fnr (oxrA) and oxrC genes, and is controlled by catabolite repression. The synthesis of the individual hydrogenase isoenzymes is also specifically influenced by fnr and oxrC mutations and by catabolite repression in a manner entirely consistent with the proposed role for each isoenzyme in hydrogen metabolism. Synthesis of hydrogenase isoenzyme 2 was found to be fnr dependent and oxrC independent, consistent with a role in respiration-linked hydrogen uptake which was shown to be similarly regulated. Also in keeping with such a respiratory role was the finding that both hydrogen uptake and the expression of isoenzyme 2 are under catabolite repression. In contrast, formate hydrogenlyase-dependent hydrogen evolution, characteristic of fermentative growth, was reduced in oxrC strains but not in fnr strains. Hydrogenase 3 activity was similarly regulated, consistent with a role in hydrogen evolution. Unlike the expression of hydrogenases 2 and 3, hydrogenase 1 expression was both fnr and oxrC dependent. Hydrogen uptake during fermentative growth was also both fnr and oxrC dependent. This provided good evidence for a distinction between hydrogen uptake during fermentation- and respiration-dependent growth and for a hydrogen-recycling process. The pattern of anaerobic control of hydrogenase activities illustrated the functional diversity of the isoenzymes and, in addition, the physiological distinction between the two anaerobic regulatory pathways, anaerobic respiratory genes being fnr dependent and enzymes required during fermentative growth being oxrC dependent.
鼠伤寒沙门氏菌中的氢代谢受到由fnr(oxrA)和oxrC基因定义的两条厌氧调节途径中的突变的差异调节,并受分解代谢物阻遏的控制。各个氢化酶同工酶的合成也受到fnr和oxrC突变以及分解代谢物阻遏的特异性影响,其方式与每种同工酶在氢代谢中所提出的作用完全一致。发现氢化酶同工酶2的合成依赖于fnr且不依赖于oxrC,这与呼吸相关的氢摄取中的作用一致,后者也显示出类似的调节方式。同样与这种呼吸作用相符的是,氢摄取和同工酶2的表达都受到分解代谢物阻遏。相比之下,发酵生长特有的甲酸氢化酶依赖性氢进化在oxrC菌株中减少,但在fnr菌株中没有减少。氢化酶3的活性也受到类似的调节,这与氢进化中的作用一致。与氢化酶2和3的表达不同,氢化酶1的表达既依赖于fnr也依赖于oxrC。发酵生长期间的氢摄取也既依赖于fnr又依赖于oxrC。这为区分发酵依赖性生长和呼吸依赖性生长期间的氢摄取以及氢循环过程提供了有力证据。氢化酶活性的厌氧控制模式说明了同工酶的功能多样性,此外,还说明了两条厌氧调节途径之间的生理区别,即厌氧呼吸基因依赖于fnr,而发酵生长期间所需的酶依赖于oxrC。