Kovacevic S, Tobin M B, Miller J R
Department of Molecular Genetics Research, Lilly Corporate Center, Indianapolis, Indiana 16285.
J Bacteriol. 1990 Jul;172(7):3952-8. doi: 10.1128/jb.172.7.3952-3958.1990.
Isopenicillin N isomerase (epimerase) has been purified from Streptomyces clavuligerus, and the amino acid sequence of the N-terminus has been determined. By using single oligonucleotide probes based on high GC codon bias ("guessmers"), the translation start codons were determined for two successive genes in the beta-lactam-biosynthetic pathway and mapped within a 3.6-kilobase-pair KpnI restriction fragment. The epimerase gene (cefD) was located immediately upstream of the deacetoxycephalosporin C synthetase (expandase) gene (cefE) that was characterized previously. cefD was sequenced and expressed in Escherichia coli; the resulting cell extracts contained epimerase activity. Western immunoblots demonstrated that a protein comigrated with purified S. clavuligerus epimerase at 44 kilodaltons. cefD and cefE were separated by an 81-base-pair segment. The DNA sequence upstream of the epimerase gene had a high AT content, suggestive of a promoter region. Primer extension analysis of S. clavuligerus mRNA showed that the start of transcription occurred approximately 130 base pairs upstream of the epimerase translation start site; Northern (RNA blot) analysis revealed a hybridization signal large enough to code for both epimerase and expandase, and nuclease S1 protection assays showed that a single message may code for epimerase, expandase, and another unknown protein. When cefD and cefE were placed in an expression vector, concomitant synthesis of both epimerase and expandase occurred in E. coli.
异青霉素N异构酶(差向异构酶)已从棒状链霉菌中纯化出来,并且已确定了其N端的氨基酸序列。通过使用基于高GC密码子偏好性的单链寡核苷酸探针(“推测引物”),确定了β-内酰胺生物合成途径中两个连续基因的翻译起始密码子,并将其定位在一个3.6千碱基对的KpnI限制性片段内。差向异构酶基因(cefD)位于先前已鉴定的去乙酰氧头孢菌素C合成酶(扩环酶)基因(cefE)的紧邻上游。对cefD进行了测序并在大肠杆菌中表达;所得细胞提取物含有差向异构酶活性。蛋白质免疫印迹表明,有一种蛋白质与纯化的棒状链霉菌差向异构酶在44千道尔顿处共迁移。cefD和cefE被一个81碱基对的片段隔开。差向异构酶基因上游的DNA序列具有高AT含量,提示为启动子区域。对棒状链霉菌mRNA进行引物延伸分析表明,转录起始点大约在差向异构酶翻译起始位点上游130个碱基对处;Northern(RNA印迹)分析显示有一个足够大的杂交信号,足以编码差向异构酶和扩环酶,核酸酶S1保护试验表明,单一的信使RNA可能编码差向异构酶、扩环酶和另一种未知蛋白质。当将cefD和cefE置于表达载体中时,在大肠杆菌中会同时合成差向异构酶和扩环酶。