Dodd H N, Pemberton J M
Department of Microbiology, University of Queensland, Australia.
J Bacteriol. 1996 Jul;178(13):3926-33. doi: 10.1128/jb.178.13.3926-3933.1996.
An Escherichia coli clone expressing activity on DNase agar was obtained by cloning chromosomal DNA of Aeromonas hydrophila JMP636 into plasmid pUC19. Examination (of the clone's nuclease activity on a sodium dodecyl sulfate (SDS)-polyacrylamide gel containing DNA as a substrate revealed an activity band at approximately 100 kDa. Subsequently, subcloning localized the gene, designated nucH, to a 3.6-kb DNA fragment (pJP9521). Southern blotting of the nucH gene against chromosomal DNA of JMP636 confirmed that it had originated from this strain and demonstrated that it was present in a single copy, although additional faint bands were also detected. Analysis of the subclone using in vivo transcription and translation revealed only a single polypeptide of approximately 110 kDa. Sequencing of pJP9521 predicted an open reading frame of 3,213 bp encoding a protein of 1,070 amino acids and having a molecular mass of 114 kDa. Comparison of the deduced nucleotide sequence and the NucH predicted protein sequence with relevant databases indicated that no known homologs have previously been identified. A signal sequence was predicted from these data, and cellular fractionation of a nucH clone in E. coli indicated that the protein was able to be processed to the periplasm. An activity similar in size was detected in an extracellular protein sample of JMP636, while inactivation of the nucH gene resulted in loss of this activity band. By native SDS-polyacrylamide gel electrophoresis, NucH substrate specificity, cofactor requirements, and sensitivity to denaturing agents were assessed.
通过将嗜水气单胞菌JMP636的染色体DNA克隆到质粒pUC19中,获得了一株在DNA酶琼脂上表现出活性的大肠杆菌克隆。对该克隆在以DNA为底物的十二烷基硫酸钠(SDS)-聚丙烯酰胺凝胶上的核酸酶活性进行检测,结果显示在约100 kDa处有一条活性带。随后,亚克隆将该基因(命名为nucH)定位到一个3.6 kb的DNA片段(pJP9521)上。用nucH基因对JMP636的染色体DNA进行Southern杂交,证实它起源于该菌株,并表明它以单拷贝形式存在,不过也检测到了其他较淡的条带。使用体内转录和翻译对亚克隆进行分析,结果显示只有一条约110 kDa的单一多肽。对pJP9521进行测序,预测其开放阅读框为3213 bp,编码一个含有1070个氨基酸、分子量为114 kDa的蛋白质。将推导的核苷酸序列和预测的NucH蛋白质序列与相关数据库进行比较,结果表明此前未鉴定出已知的同源物。根据这些数据预测了一个信号序列,在大肠杆菌中对nucH克隆进行细胞分级分离表明该蛋白质能够被加工转运到周质中。在JMP636的细胞外蛋白质样品中检测到了一条大小相似的活性带,而nucH基因失活导致该活性带消失。通过非变性SDS-聚丙烯酰胺凝胶电泳,评估了NucH的底物特异性、辅因子需求以及对变性剂的敏感性。