Felder M, Gupta A, Verma V, Kumar A, Qazi G N, Cullum J
LB Genetik, Universität Kaiserlautern, Postfach 3049, Germany.
FEMS Microbiol Lett. 2000 Dec 15;193(2):231-6. doi: 10.1111/j.1574-6968.2000.tb09429.x.
A Tn5-induced glucose dehydrogenase (GDH) deficient mutant of Gluconobacter oxydans IFO 3293 was characterised. DNA sequencing showed that the insertion site occurred in an open reading frame with homology to the pqqE gene. It was shown that acid production could be restored by addition of the coenzyme pyrroloquinoline quinone (PQQ) to the medium. The pqq cluster of G. oxydans ATCC 9937 was cloned and sequenced. It has five genes pqqA-E. The cluster could complement the Tn5-induced mutation in IFO 3293. Pulsed-field gel electrophoresis suggested that the pqq genes are not closely linked to the ribF gene that produces the riboflavin cofactor for the gluconic acid dehydrogenase.
对氧化葡萄糖杆菌IFO 3293的一个Tn5诱导的葡萄糖脱氢酶(GDH)缺陷型突变体进行了表征。DNA测序表明,插入位点出现在一个与pqqE基因具有同源性的开放阅读框中。结果表明,向培养基中添加辅酶吡咯喹啉醌(PQQ)可以恢复酸的产生。对氧化葡萄糖杆菌ATCC 9937的pqq基因簇进行了克隆和测序。它有五个基因pqqA - E。该基因簇可以弥补IFO 3293中Tn5诱导的突变。脉冲场凝胶电泳表明,pqq基因与为葡萄糖酸脱氢酶产生核黄素辅因子的ribF基因没有紧密连锁。