Jin S, Sonenshein A L
Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts 02111.
J Bacteriol. 1994 Aug;176(15):4669-79. doi: 10.1128/jb.176.15.4669-4679.1994.
Two distinct Bacillus subtilis genes (citA and citZ) were found to encode citrate synthase isozymes that catalyze the first step of the Krebs cycle. The citA gene was cloned by genetic complementation of an Escherichia coli citrate synthase mutant strain (W620) and was in a monocistronic transcriptional unit. A divergently transcribed gene, citR, could encode a protein with strong similarity to the bacterial LysR family of regulatory proteins. A null mutation in citA had little effect on citrate synthase enzyme activity or sporulation. The residual citrate synthase activity was purified from a citA null mutant strain, and the partial amino acid sequence for the purified protein (CitZ) was determined. The citZ gene was cloned from B. subtilis chromosomal DNA by using a PCR-generated probe synthesized with oligonucleotide primers derived from the partial amino acid sequence of purified CitZ. The citZ gene proved to be the first gene in a tricistronic cluster that also included citC (coding for isocitrate dehydrogenase) and citH (coding for malate dehydrogenase). A mutation in citZ caused a substantial loss of citrate synthase enzyme activity, glutamate auxotrophy, and a defect in sporulation.
已发现两个不同的枯草芽孢杆菌基因(citA和citZ)编码柠檬酸合酶同工酶,这些同工酶催化三羧酸循环的第一步。通过对大肠杆菌柠檬酸合酶突变株(W620)进行遗传互补克隆了citA基因,该基因位于一个单顺反子转录单元中。一个反向转录的基因citR可能编码一种与细菌LysR家族调节蛋白有高度相似性的蛋白质。citA中的无效突变对柠檬酸合酶的酶活性或芽孢形成影响很小。从citA无效突变株中纯化出残留的柠檬酸合酶活性,并测定了纯化蛋白(CitZ)的部分氨基酸序列。通过使用由纯化的CitZ部分氨基酸序列衍生的寡核苷酸引物合成的PCR产生的探针,从枯草芽孢杆菌染色体DNA中克隆了citZ基因。结果证明,citZ基因是一个三顺反子簇中的第一个基因,该簇还包括citC(编码异柠檬酸脱氢酶)和citH(编码苹果酸脱氢酶)。citZ中的突变导致柠檬酸合酶酶活性大幅丧失、谷氨酸营养缺陷以及芽孢形成缺陷。