Finan T M, Weidner S, Wong K, Buhrmester J, Chain P, Vorhölter F J, Hernandez-Lucas I, Becker A, Cowie A, Gouzy J, Golding B, Pühler A
Department of Biology, McMaster University, Hamilton, ON, Canada.
Proc Natl Acad Sci U S A. 2001 Aug 14;98(17):9889-94. doi: 10.1073/pnas.161294698. Epub 2001 Jul 31.
Analysis of the 1,683,333-nt sequence of the pSymB megaplasmid from the symbiotic N(2)-fixing bacterium Sinorhizobium meliloti revealed that the replicon has a high gene density with a total of 1,570 protein-coding regions, with few insertion elements and regions duplicated elsewhere in the genome. The only copies of an essential arg-tRNA gene and the minCDE genes are located on pSymB. Almost 20% of the pSymB sequence carries genes encoding solute uptake systems, most of which were of the ATP-binding cassette family. Many previously unsuspected genes involved in polysaccharide biosynthesis were identified and these, together with the two known distinct exopolysaccharide synthesis gene clusters, show that 14% of the pSymB sequence is dedicated to polysaccharide synthesis. Other recognizable gene clusters include many involved in catabolic activities such as protocatechuate utilization and phosphonate degradation. The functions of these genes are consistent with the notion that pSymB plays a major role in the saprophytic competence of the bacteria in the soil environment.
对共生固氮细菌苜蓿中华根瘤菌(Sinorhizobium meliloti)的pSymB大质粒的1,683,333 nt序列分析表明,该复制子具有高基因密度,共有1,570个蛋白质编码区,插入元件很少,且基因组中其他地方没有重复区域。必需的精氨酸tRNA基因和minCDE基因的唯一拷贝位于pSymB上。几乎20%的pSymB序列携带编码溶质摄取系统的基因,其中大多数属于ATP结合盒家族。鉴定出许多以前未被怀疑的参与多糖生物合成的基因,这些基因与两个已知的不同胞外多糖合成基因簇一起表明,14%的pSymB序列专门用于多糖合成。其他可识别的基因簇包括许多参与分解代谢活动的基因簇,如原儿茶酸利用和膦酸盐降解。这些基因的功能与pSymB在土壤环境中细菌腐生能力中起主要作用的观点一致。