Novak P D, Maier R J
J Bacteriol. 1987 Jun;169(6):2708-12. doi: 10.1128/jb.169.6.2708-2712.1987.
Derepression of an uptake hydrogenase in Bradyrhizobium japonicum is dependent on a microaerophilic environment. Addition of DNA gyrase inhibitors during depression of hydrogenase specifically prevented expression of the hydrogenase enzyme. Antibodies to individual hydrogenase subunits failed to detect the protein after derepression in the presence of inhibitors, although there was no general inhibition of protein synthesis. The general pattern of proteins synthesized from 14C-labeled amino acids during derepression was not significantly different whether proteins were labeled in the presence or in the absence of gyrase inhibitors. In contrast, if transcription or translation was inhibited by addition of inhibitors of those functions, virtually no proteins were labeled during derepression. This indicated that most of the 14C-labeled proteins were synthesized de novo during derepression, synthesis of most proteins was unaffected by gyrase inhibitors, and the dependence of hydrogenase synthesis on gyrase activity was a specific one.
慢生根瘤菌中摄取型氢化酶的去阻遏依赖于微需氧环境。在氢化酶阻遏期间添加DNA促旋酶抑制剂可特异性地阻止氢化酶的表达。尽管蛋白质合成没有受到普遍抑制,但在抑制剂存在下去阻遏后,针对单个氢化酶亚基的抗体未能检测到该蛋白质。在去阻遏过程中,无论蛋白质标记是在促旋酶抑制剂存在还是不存在的情况下进行,由14C标记氨基酸合成的蛋白质的总体模式没有显著差异。相反,如果通过添加转录或翻译功能抑制剂来抑制转录或翻译,则在去阻遏过程中几乎没有蛋白质被标记。这表明大多数14C标记的蛋白质是在去阻遏过程中重新合成的,大多数蛋白质的合成不受促旋酶抑制剂的影响,并且氢化酶合成对促旋酶活性的依赖性是特异性的。