Koebmann B J, Nilsson D, Kuipers O P, Jensen P R
Department of Microbiology, Technical University of Denmark, DK-2800 Lyngby, Denmark.
J Bacteriol. 2000 Sep;182(17):4738-43. doi: 10.1128/JB.182.17.4738-4743.2000.
The eight genes which encode the (F(1)F(o)) H(+)-ATPase in Lactococcus lactis subsp. cremoris MG1363 were cloned and sequenced. The genes were organized in an operon with the gene order atpEBFHAGDC; i.e., the order of atpE and atpB is reversed with respect to the more typical bacterial organization. The deduced amino acid sequences of the corresponding H(+)-ATPase subunits showed significant homology with the subunits from other organisms. Results of Northern blot analysis showed a transcript at approximately 7 kb, which corresponds to the size of the atp operon. The transcription initiation site was mapped by primer extension and coincided with a standard promoter sequence. In order to analyze the importance of the H(+)-ATPase for L. lactis physiology, a mutant strain was constructed in which the original atp promoter on the chromosome was replaced with an inducible nisin promoter. When grown on GM17 plates the resulting strain was completely dependent on the presence of nisin for growth. These data demonstrate that the H(+)-ATPase is essential for growth of L. lactis under these conditions.
对乳酸乳球菌亚种cremoris MG1363中编码(F(1)F(o))H(+) - ATP酶的8个基因进行了克隆和测序。这些基因以操纵子形式排列,基因顺序为atpEBFHAGDC;也就是说,与更典型的细菌组织相比,atpE和atpB的顺序是相反的。相应的H(+) - ATP酶亚基的推导氨基酸序列与其他生物体的亚基具有显著同源性。Northern印迹分析结果显示,在约7 kb处有一条转录本,这与atp操纵子的大小相对应。通过引物延伸确定了转录起始位点,该位点与标准启动子序列一致。为了分析H(+) - ATP酶对乳酸乳球菌生理学的重要性,构建了一个突变菌株,其中染色体上的原始atp启动子被可诱导的乳链菌肽启动子取代。当在GM17平板上生长时,所得菌株的生长完全依赖于乳链菌肽的存在。这些数据表明,在这些条件下,H(+) - ATP酶对乳酸乳球菌的生长至关重要。