Chen C C, Liao C C, Hsu W H
Culture Collection and Research Center, Food Industry Research and Development Institute, Hsinchu, Taiwan.
FEMS Microbiol Lett. 1993 Mar 1;107(2-3):223-9. doi: 10.1111/j.1574-6968.1993.tb06034.x.
The aro gene of Corynebacterium glutamicum CCRC 18310 encoding 3-deoxy-D-arabinoheptulosonate-7-phosphate (DAHP) synthase was isolated by complementation of a DAHP synthase-deficient mutant of Escherichia coli AB3257. The specific activity of DAHP synthase was increased four-fold in a C. glutamicum strain harboring the cloned aro gene. The complete nucleotide sequence of the aro gene and its 5' and 3' flanking regions has been determined. The sequence contained an open reading frame of 368 codons, from which a protein with a molecular mass of 39,340 Da could be predicted. The deduced amino acid sequence shows high identity with the aro gene products of E. coli and Salmonella typhimurium.
通过对大肠杆菌AB3257的3-脱氧-D-阿拉伯庚酮糖-7-磷酸(DAHP)合酶缺陷型突变体进行互补,分离出了谷氨酸棒杆菌CCRC 18310中编码DAHP合酶的aro基因。在携带克隆aro基因的谷氨酸棒杆菌菌株中,DAHP合酶的比活性提高了四倍。已确定aro基因及其5'和3'侧翼区域的完整核苷酸序列。该序列包含一个368个密码子的开放阅读框,据此可预测出一个分子量为39,340 Da的蛋白质。推导的氨基酸序列与大肠杆菌和鼠伤寒沙门氏菌的aro基因产物具有高度同源性。