Kim Jung-Gun, Park Byoung Keun, Kim Sung-Uk, Choi Doil, Nahm Baek Hie, Moon Jae Sun, Reader John S, Farrand Stephen K, Hwang Ingyu
School of Agricultural Biotechnology and Center for Agricultural Biomaterials, Seoul National University, Seoul 151-921, Korea.
Proc Natl Acad Sci U S A. 2006 Jun 6;103(23):8846-51. doi: 10.1073/pnas.0602965103. Epub 2006 May 26.
Agrobacterium radiobacter K84, used worldwide to biocontrol crown gall disease caused by Agrobacterium tumefaciens, produces an antiagrobacterial compound called agrocin 84. We report the nucleotide sequence of pAgK84, a 44.42-kb plasmid coding for production of this disubstituted adenine nucleotide antibiotic. pAgK84 encodes 36 ORFs, 17 of which (agn) code for synthesis of or immunity to agrocin 84. Two genes, agnB2 and agnA, encode aminoacyl tRNA synthetase homologues. We have shown that the toxic moiety of agrocin 84 inhibits cellular leucyl-tRNA synthetases and AgnB2, which confers immunity to the antibiotic, is a resistant form of this enzyme. AgnA, a truncated homologue of asparaginyl tRNA synthetase could catalyze the phosphoramidate bond between a precursor of the methyl pentanamide side group and the nucleotide. We propose previously undescribed chemistry, catalyzed by AgnB1, to generate the precursor necessary for this phosphoramidate linkage. AgnC7 is related to ribonucleotide reductases and could generate the 3'-deoxyarabinose moiety of the nucleoside. Bioinformatics suggest that agnC3, agnC4, and agnC6 contribute to maturation of the methyl pentanamide, whereas agnC2 may produce the glucofuranose side group bound to the adenine ring. AgnG is related to bacterial exporters. An agnG mutant accumulated agrocin 84 intracellularly but did not export the antibiotic. pAgK84 is transmissible and encodes genes for conjugative DNA processing but lacks a type IV secretion system, suggesting that pAgK84 transfers by mobilization. By sequence analysis, the deletion engineered into pAgK1026 removed the oriT and essential tra genes, confirming the enhanced environmental safety of this modified form of pAgK84.
放射土壤杆菌K84在全球范围内用于生物防治由根癌土壤杆菌引起的冠瘿病,它能产生一种名为农杆菌素84的抗菌化合物。我们报道了pAgK84的核苷酸序列,这是一个44.42 kb的质粒,编码这种二取代腺嘌呤核苷酸抗生素的产生。pAgK84编码36个开放阅读框(ORF),其中17个(agn)编码农杆菌素84的合成或免疫相关基因。两个基因agnB2和agnA编码氨酰tRNA合成酶同源物。我们已经表明,农杆菌素84的毒性部分抑制细胞亮氨酰tRNA合成酶,而赋予对抗生素免疫性的AgnB2是这种酶的抗性形式。AgnA是天冬酰胺tRNA合成酶的截短同源物,可催化甲基戊酰胺侧基前体与核苷酸之间的磷酰胺键。我们提出由AgnB1催化的前所未描述的化学反应,以产生这种磷酰胺连接所需的前体。AgnC7与核糖核苷酸还原酶相关,可产生核苷的3'-脱氧阿拉伯糖部分。生物信息学表明,agnC3、agnC4和agnC6有助于甲基戊酰胺的成熟,而agnC2可能产生与腺嘌呤环结合的呋喃葡萄糖侧基。AgnG与细菌外排蛋白相关。AgnG突变体在细胞内积累了农杆菌素84,但不分泌抗生素。pAgK84是可转移的,编码用于接合DNA加工的基因,但缺乏IV型分泌系统,这表明pAgK84通过迁移进行转移。通过序列分析,pAgK1026中设计的缺失去除了oriT和必需的tra基因,证实了这种修饰形式的pAgK84具有更高的环境安全性。