Borghese R, Turina P, Lambertini L, Melandri B A
Università di Bologna, Dipartimento di Biologia, Italy.
Arch Microbiol. 1998 Oct;170(5):385-8. doi: 10.1007/s002030050657.
The atpIBEXF operon coding for the F0 sector of the ATP synthase from Rhodobacter capsulatus was cloned and sequenced. The genes for the five subunits were present in the order: atpI (subunit I), atpB (subunit a), atpE (subunit c), atpX (subunit b'), and atpF (subunit b). The transcription initiation site was defined by primer-extension analysis. A duplicated and divergent copy of the b subunit gene (subunit b') was present. This duplication is found only in photosynthetic prokaryotes and in plant chloroplasts. F0 deletion mutants formed tiny colonies during anaerobic growth in the dark but could not sustain continuous growth. Based on the results of the present work, we conclude that a functioning ATP synthase is essential for normal growth under all conditions tested.
编码荚膜红细菌ATP合酶F0部分的atpIBEXF操纵子被克隆并测序。五个亚基的基因按以下顺序排列:atpI(亚基I)、atpB(亚基a)、atpE(亚基c)、atpX(亚基b')和atpF(亚基b)。转录起始位点通过引物延伸分析确定。存在b亚基基因(亚基b')的重复且不同向的拷贝。这种重复仅在光合原核生物和植物叶绿体中发现。F0缺失突变体在黑暗中厌氧生长期间形成微小菌落,但无法维持持续生长。基于目前的工作结果,我们得出结论,在所有测试条件下,正常运作的ATP合酶对于正常生长至关重要。