将转座子Tn5插入到泛tropha的膜结合硝酸盐还原酶的结构基因中,导致质周硝酸盐还原酶活性的厌氧过表达。

L C Bell, M D Page, B C Berks, D J Richardson, S J Ferguson
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引用次数: 48

摘要

利用转座子Tn5诱变法,获得了反硝化细菌硫磷菌的耐氯酸盐突变体。一类缺乏膜结合的硝酸盐还原酶活性,但保留了质周的硝酸盐还原酶活性。利用转座子标记修复,在一个这样的突变体M-6中,转座子插入到膜结合的硝酸盐还原酶β亚基结构基因(命名为narH,以与大肠杆菌主要硝酸盐还原酶操纵子的命名一致)。转座子插入点附近的翻译序列(共106个氨基酸)显示与大肠杆菌硝酸盐还原酶的β亚基的氨基酸一致性约为90%。在厌氧生长条件下,M-6产生过多的质周硝酸盐还原酶活性,允许以硝酸盐作为电子受体进行厌氧生长。在膜结合的硝酸盐还原酶的存在和质周硝酸盐还原酶的表达之间推断出一种调节联系。这是首次在仅具有质周硝酸盐还原酶的生物体中完全反硝化的演示。
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Insertion of transposon Tn5 into a structural gene of the membrane-bound nitrate reductase of Thiosphaera pantotropha results in anaerobic overexpression of periplasmic nitrate reductase activity.

Chlorate-resistant mutants of the denitrifying bacterium Thiosphaera pantotropha were generated by transposon Tn5 mutagenesis. One class was deficient in membrane-bound nitrate reductase activity but retained a periplasmic nitrate reductase activity. Using transposon marker rescue it was shown that in one such mutant, M-6, the transposon was inserted in the membrane-bound nitrate reductase beta subunit structural gene (termed narH in order to be consistent with the nomenclature of the Escherichia coli major nitrate reductase operon). The translated sequence (total of 106 amino acids) from around the point of transposon insertion showed approximately 90% amino acid identity with the beta subunits of the E. coli nitrate reductases. Under anaerobic growth conditions M-6 overproduced the periplasmic nitrate reductase activity allowing anaerobic growth with nitrate as electron acceptor. A regulatory link was inferred between the presence of the membrane-bound nitrate reductase and expression of the periplasmic nitrate reductase. This is the first demonstration of full denitrification in an organism possessing only a periplasmic nitrate reductase.

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