Sakata N, Minamitani S, Kanbe T, Hori M, Hamada M, Edo K
Showa College of Pharmaceutical Sciences, Tokyo, Japan.
Biol Pharm Bull. 1993 Jan;16(1):26-8. doi: 10.1248/bpb.16.26.
A segment of the neocarzinostatin apoprotein gene corresponding to T30 to A91 of the protein was amplified using a polymerase chain reaction (PCR) with total DNA from Streptomyces carzinostaticus subsp. neocarzinostaticus E-793 (ATCC 15944) as the template and with 5'- and 3'-primers synthesized in consideration of the codon usage of streptomyces. The PCR product was cloned, sequenced and confirmed to direct an amino acid sequence reasonably well matching that reported. Using the PCR product as a probe, we cloned a DNA segment (2580 bp) spanning an open reading frame (ORF) for preapoprotein (leader peptide plus apoprotein) and its upstream and downstream flanking regions. The amino acid sequence deduced from the base sequence of the DNA clearly identified those amino acid residues which had remained inconsistent among different research groups. The base sequence homology with other apoprotein genes of related antibiotics was analyzed and was found to be limited within the structural gene.
以新制癌菌素产生菌(Streptomyces carzinostaticus subsp. neocarzinostaticus)E-793(ATCC 15944)的总DNA为模板,使用聚合酶链反应(PCR)扩增新制癌菌素脱辅基蛋白基因中与该蛋白质T30至A91相对应的片段,并使用考虑链霉菌密码子使用情况合成的5'和3'引物。PCR产物被克隆、测序,并确认其指导的氨基酸序列与报道的序列相当匹配。以PCR产物为探针,我们克隆了一个跨越前脱辅基蛋白(前导肽加脱辅基蛋白)开放阅读框(ORF)及其上游和下游侧翼区域的DNA片段(2580 bp)。从该DNA的碱基序列推导的氨基酸序列清楚地鉴定了不同研究组之间仍不一致的那些氨基酸残基。分析了与相关抗生素其他脱辅基蛋白基因的碱基序列同源性,发现其在结构基因内有限。