Eikmanns B J, Follettie M T, Griot M U, Sinskey A J
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
Mol Gen Genet. 1989 Aug;218(2):330-9. doi: 10.1007/BF00331286.
The ppc gene of Corynebacterium glutamicum encoding phosphoenolpyruvate (PEP) carboxylase was isolated by complementation of a ppc mutant of Escherichia coli using a cosmid gene bank of chromosomal C. glutamicum DNA. By subsequent subcloning into the plasmid pUC8 and deletion analysis, the ppc gene could be located on a 3.3 kb SalI fragment. This fragment was able to complement the E. coli ppc mutant and conferred PEP carboxylase activity to the mutant. The complete nucleotide sequence of the ppc gene including 5' and 3' flanking regions has been determined and the primary structure of PEP carboxylase was deduced. The sequence predicts a 919 residue protein product (molecular weight of 103 154) which shows 34% similarity with the respective E. coli enzyme.
利用谷氨酸棒杆菌染色体DNA的黏粒基因文库,通过对大肠杆菌ppc突变体进行互补,分离出了谷氨酸棒杆菌中编码磷酸烯醇式丙酮酸(PEP)羧化酶的ppc基因。通过随后亚克隆到质粒pUC8中并进行缺失分析,可将ppc基因定位在一个3.3 kb的SalI片段上。该片段能够互补大肠杆菌的ppc突变体,并赋予该突变体PEP羧化酶活性。已确定了包括5'和3'侧翼区域在内的ppc基因的完整核苷酸序列,并推导了PEP羧化酶的一级结构。该序列预测有一个919个残基的蛋白质产物(分子量为103 154),与相应的大肠杆菌酶有34%的相似性。