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嗜碱芽孢杆菌OF4编码一种ABC型转运蛋白的染色体区域的序列分析和功能研究,该转运蛋白在序列和Na⁺排除能力上与枯草芽孢杆菌NatAB转运蛋白相似。

Sequence analysis and functional studies of a chromosomal region of alkaliphilic Bacillus firmus OF4 encoding an ABC-type transporter with similarity of sequence and Na+ exclusion capacity to the Bacillus subtilis NatAB transporter.

作者信息

Wei Y, Guffanti A A, Krulwich T A

机构信息

Department of Biochemistry, Mount Sinai School of Medicine, New York, NY 10029, USA.

出版信息

Extremophiles. 1999 May;3(2):113-20. doi: 10.1007/s007920050106.

DOI:10.1007/s007920050106
PMID:10356997
Abstract

A 14.1-kb DNA fragment was cloned from a lambda library containing inserts of DNA from alkaliphilic Bacillus firmus OF4 on the basis of its hybridization to a probe from a previously sequenced alkaliphile homolog of the natA gene from Bacillus subtilis. Sequence analysis of the entire fragment revealed that, as in B. subtilis, the natA gene was part of a putative gene locus encoding an ABC-type transporter. In the alkaliphile, the transporter involved three genes, designated natCAB, that are part of a larger operon of unknown function. This is in contrast to the two-gene natAB operon and to another homolog from B. subtilis, the yhaQP genes. Like natAB, however, the alkaliphile natCAB catalyzes Na+ extrusion as assessed in a mutant of Escherichia coli that is deficient in Na+ extrusion. The full 14.1-kb fragment of alkaliphile DNA sequenced in this study contained several probable operons as well as likely monocistronic units. Among the 17 predicted ORFs apart from natCAB were acsA, a homolog of a halobacterial gene encoding acetylCoA synthetase; sspA, a homolog of a small acid-soluble spore protein; and malK, an ATP-binding component that was unaccompanied by candidates for other mal transport genes but was able to complement a malK-deficient mutant of E. coli. No strong candidates for genes encoding a secondary Na+/H+ antiporter were found in the fragment, either from the sequence analysis or from analyses of complementation of E. coli mutants by subclones of the 14.1-kb piece. There were a total of 12 ORFs whose closest and significant homologs were genes from B. subtilis; of these, one-third were in apparently different contexts, as assessed by the sequence of the neighboring genes, than the B. subtilis homologs.

摘要

基于与枯草芽孢杆菌中先前测序的嗜碱菌natA基因同源物探针的杂交,从一个包含嗜碱芽孢杆菌OF4 DNA插入片段的λ文库中克隆出一个14.1 kb的DNA片段。对整个片段的序列分析表明,与枯草芽孢杆菌一样,natA基因是一个推定的编码ABC型转运蛋白的基因座的一部分。在嗜碱菌中,该转运蛋白涉及三个基因,命名为natCAB,它们是一个功能未知的更大操纵子的一部分。这与双基因natAB操纵子以及枯草芽孢杆菌的另一个同源物yhaQP基因形成对比。然而,与natAB一样,嗜碱菌natCAB在缺乏Na+ 外排的大肠杆菌突变体中评估时可催化Na+ 外排。本研究中测序的14.1 kb嗜碱菌DNA完整片段包含几个可能的操纵子以及可能的单顺反子单元。除natCAB外的17个预测开放阅读框中,有acsA,它是编码乙酰辅酶A合成酶的嗜盐细菌基因的同源物;sspA,一种小的酸溶性孢子蛋白的同源物;以及malK,一个ATP结合成分,它没有其他mal转运基因的候选物相伴,但能够互补大肠杆菌的malK缺陷突变体。无论是从序列分析还是从14.1 kb片段的亚克隆对大肠杆菌突变体的互补分析中,在该片段中都未发现编码次级Na+/H+ 反向转运蛋白的基因的有力候选物。总共有12个开放阅读框,其最接近且显著的同源物是枯草芽孢杆菌的基因;其中三分之一与枯草芽孢杆菌同源物相比,根据相邻基因的序列评估,其所处环境明显不同。

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