Cloning and molecular characterization of the atp operon encoding for the F1F0-ATP synthase from a thermoalkaliphilic Bacillus sp strain TA2.A1

被引:17
作者
Keis, S
Kaim, G
Dimroth, P
Cook, GM [1 ]
机构
[1] Univ Otago, Otago Sch Med Sci, Dept Microbiol, Dunedin, New Zealand
[2] ETH Zentrum, Inst Mikrobiol, CH-8092 Zurich, Switzerland
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 2004年 / 1676卷 / 01期
关键词
thermoalkaliphilic Bacillus sp; F1F0-ATP synthase; atp operon; Northern hybridization;
D O I
10.1016/j.bbaexp.2003.11.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The genes encoding the subunits for the F1F0-ATP synthase from Bacillus sp. strain TA2.A1 were cloned as three overlapping fragments and sequenced. The nine genes were organized in an operon with the gene order atpIBEFHAGDC encoding the i, a, c, b, delta, alpha, gamma, beta, and epsilon subunits, respectively. Northern blot analysis showed a maximum transcript of approximately 7.2 kb, which corresponds to the size of the atp operon and demonstrated that the nine genes are transcribed as a single polycistronic message. The alkaliphilic-specific residues Lys(218) and Gly(245) were conserved in subunit a of strain TA2.A1 Analysis of the C-terminal domain of the a subunit showed several clusters of basic residues which are predicted to form a strong electrostatic interaction with the DELSDED motif in the beta subunit from strain TA2.A1, and may explain the blockage of this enzyme in the ATP hydrolysis direction. (C) 2003 Elsevier B.V All rights reserved.
引用
收藏
页码:112 / 117
页数:6
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