Page M D, Ferguson S J
Department of Biochemistry, University of Oxford, UK.
Mol Microbiol. 1995 Jan;15(2):307-18. doi: 10.1111/j.1365-2958.1995.tb02245.x.
A transposon Tn5 mutant of Paracoccus denitrificans, DP108, was incapable of anaerobic or methylotrophic growth and scored negative in the Nadi cytochrome c oxidase test. P. denitrificans DP108 grown aerobically on succinate or choline was devoid of soluble c-type cytochromes and accumulated periplasmic apocytochrome c550, but the membrane-bound holocytochromes c1 and c552 were present at 5-10% of the levels observed in wild-type cells. DP108 genomic DNA flanking the site of Tn5 insertion was cloned by marker rescue and used to probe a P. denitrificans wild-type DNA library. A hybridizing 3.05 kb BamHI fragment capable of complementing the DP108 mutation was isolated and a 2.05 kb region of this was sequenced. One major open reading frame equivalent to 413 amino acids was identified, the predicted product of which was similar (33% identity, 55% similarity) to the predicted product of the cycH gene previously identified in Bradyrhizobium japonicum. Similarity of the two cycH gene products to the predicted products of two Escherichia coli genes, nrfG and yejP, was also detected. Significant differences between the phenotypes of P. denitrificans DP108 and the B. japonicum cycH mutant COX3, especially with respect to cytochrome c1 synthesis, suggest that the cycH gene product may be an assembly factor.
反硝化副球菌的转座子Tn5突变体DP108无法进行厌氧生长或甲基营养生长,且在纳迪细胞色素c氧化酶试验中呈阴性。在琥珀酸盐或胆碱上需氧生长的反硝化副球菌DP108缺乏可溶性c型细胞色素,并积累了周质脱辅基细胞色素c550,但膜结合的全细胞色素c1和c552的含量仅为野生型细胞中观察到的水平的5 - 10%。通过标记拯救克隆了Tn5插入位点侧翼的DP108基因组DNA,并用于探测反硝化副球菌野生型DNA文库。分离出一个能够互补DP108突变的3.05 kb BamHI杂交片段,并对其中2.05 kb区域进行了测序。鉴定出一个相当于413个氨基酸的主要开放阅读框,其预测产物与先前在日本慢生根瘤菌中鉴定的cycH基因的预测产物相似(同一性为33%,相似性为55%)。还检测到这两个cycH基因产物与两个大肠杆菌基因nrfG和yejP的预测产物的相似性。反硝化副球菌DP108和日本慢生根瘤菌cycH突变体COX3的表型之间存在显著差异,特别是在细胞色素c1合成方面,这表明cycH基因产物可能是一种组装因子。