Komatsu Harunobu, Imura Yoshiyuki, Ohori Akira, Nagata Yuji, Tsuda Masataka
Department of Environmental Life Sciences, Graduate School of Life Sciences, Tohoku University, Sendai 980-8577, Japan.
J Bacteriol. 2003 Jun;185(11):3333-43. doi: 10.1128/JB.185.11.3333-3343.2003.
The Burkholderia multivorans strain ATCC 17616 carries three circular chromosomes with sizes of 3.4, 2.5, and 0.9 Mb. To determine the distribution and organization of the amino acid biosynthetic genes on the genome of this beta-proteobacterium, various auxotrophic mutations were isolated using a Tn5 derivative that was convenient not only for the determination of its insertion site on the genome map but also for the structural analysis of the flanking regions. Analysis by pulsed-field gel electrophoresis revealed that 20 out of 23 insertion mutations were distributed on the 3.4-Mb chromosome. More detailed analysis of the his, trp, arg, and lys mutations and their flanking regions revealed the following properties of these auxotrophic genes: (i) all nine his genes were clustered on the 3.4-Mb chromosome; (ii) seven trp genes were organized within two distinct regions, i.e., a trpEGDC cluster on the 3.4-Mb chromosome and a trpFBA cluster on the 2.5-Mb chromosome; (iii) the leu gene cluster, leuCDB, was also located close to the trpFBA cluster; and (iv) lysA and argG genes were located on the 2.5-Mb chromosome, in contrast to the argH gene, which was located on the 3.4-Mb chromosome. Southern hybridization analysis, allelic exchange mutagenesis of ATCC 17616, and complementation tests demonstrated that all of the genes examined were functional and existed as a single copy within the genome. The present findings also indicated that the 2.5-Mb chromosome carried various auxotrophic genes with no structural or functional counterparts on the remaining two chromosomes.
多食伯克霍尔德菌菌株ATCC 17616携带三条环状染色体,大小分别为3.4 Mb、2.5 Mb和0.9 Mb。为了确定这种β-变形菌基因组上氨基酸生物合成基因的分布和组织情况,使用一种Tn5衍生物分离了各种营养缺陷型突变体,该衍生物不仅便于确定其在基因组图谱上的插入位点,还便于对侧翼区域进行结构分析。脉冲场凝胶电泳分析表明,23个插入突变中有20个分布在3.4 Mb的染色体上。对组氨酸、色氨酸、精氨酸和赖氨酸突变及其侧翼区域进行更详细的分析,揭示了这些营养缺陷型基因的以下特性:(i) 所有九个组氨酸基因都聚集在3.4 Mb的染色体上;(ii) 七个色氨酸基因分布在两个不同的区域,即3.4 Mb染色体上的trpEGDC簇和2.5 Mb染色体上的trpFBA簇;(iii) 亮氨酸基因簇leuCDB也位于trpFBA簇附近;(iv) 赖氨酸A和精氨酸G基因位于2.5 Mb的染色体上,而精氨酸H基因位于3.4 Mb的染色体上。Southern杂交分析、ATCC 17616的等位基因交换诱变和互补试验表明,所有检测的基因都是有功能的,并且在基因组中以单拷贝形式存在。目前的研究结果还表明,2.5 Mb的染色体携带了各种营养缺陷型基因,而其余两条染色体上没有结构或功能对应的基因。