Sashihara T, Kimura H, Higuchi T, Adachi A, Matsusaki H, Sonomoto K, Ishizaki A
Department of Bioscience and Biotechnology, Graduate School of Agriculture, Kyushu University, Fukuoka, Japan.
Biosci Biotechnol Biochem. 2000 Nov;64(11):2420-8. doi: 10.1271/bbb.64.2420.
Staphylococcus warneri ISK-1, which we had previously reported as Pediococcus sp. ISK-1, produces a novel bacteriocin, nukacin ISK-1. Edman degradation of the chemically reduced nukacin ISK-1 produced a sequence of 27 amino acids, 7 of which were unidentified. Using single-specific-primer-PCR product as a probe, a 3.6-kb HindIII fragment containing the nukacin ISK-1 structural gene (nukA) was cloned and sequenced. The deduced amino acid sequence of nukacin ISK-1 had 57 amino acids, including a 30-amino acid leader region. The propeptide sequence showed significant similarity to those of lacticin-481 type lantibiotics. In the region upstream of nukA, a part of a long open reading frame (ORF), designated as nukM, encoding a putative modification enzyme was oriented in the opposite direction. In the region downstream of nukA, ORF1 was found in which the sequence of the putative translational product was similar to various response regulatory proteins.
沃纳葡萄球菌ISK-1,我们之前曾将其报道为嗜盐四联球菌ISK-1,可产生一种新型细菌素——诺卡菌素ISK-1。对化学还原后的诺卡菌素ISK-1进行埃德曼降解,得到了一段由27个氨基酸组成的序列,其中7个氨基酸无法识别。以单特异性引物PCR产物为探针,克隆并测序了一个包含诺卡菌素ISK-1结构基因(nukA)的3.6 kb HindIII片段。推导的诺卡菌素ISK-1氨基酸序列有57个氨基酸,包括一个30个氨基酸的前导区。前肽序列与乳酸链球菌素481型羊毛硫抗生素的前肽序列具有显著相似性。在nukA上游区域,一个长开放阅读框(ORF)的一部分,命名为nukM,编码一种假定的修饰酶,其方向相反。在nukA下游区域,发现了ORF1,其中假定翻译产物的序列与各种应答调节蛋白相似。