Bassam B J, Djordjevic M A, Redmond J W, Batley M, Rolfe B G
Research School of Biological Sciences, Australian National University, Canberra.
Mol Plant Microbe Interact. 1988 Apr;1(4):161-8. doi: 10.1094/mpmi-1-161.
Transfer of the strain NGR234nodD 1 gene into the narrow host range R. trifolii strain ANU843 on either a 6.7-kb HindIII or 17-kb XhoI fragment broadens the host range of this bacterium to include the tropical legumes Vigna unguiculata, Glycine ussuriensis, Leucaena leucocephala, and siratro (Macroptilium atropurpureum). Contrary to previous data (Bassam et al. 1986), mutagenesis of the 17-kb XhoI fragment with a mini-Mu lac transposon (Mu dII1734) showed that a functional nodD 1 gene was essential for extended host range. Gene expression studies using both Mu dII1734 fusions and a promoter-cloning vector indicated that several loci, including the nodD 1 gene, are constitutively expressed. No evidence was found for regulation of the strain NGR234 nodD 1 gene by its product. Another locus nod-81, was induced only in the presence of exudates from various plant species, including soybean (Glycine max). Whereas the expression of nod-81 was dependent on the presence of a functional nodD 1 gene product, a regulatory nod-box DNA sequence was not detected 5' to this gene by using available oligonucleotide hybridization probes. The nod-81 locus was induced by genistein, daidzein, naringenin, and coumestrol from both cotyledon and root tissue of freshly germinated soybean seedlings. A broad spectrum of commercially available phenolic compounds stimulated induction of the nod-81 locus, including some that antagonize nod gene induction in other Rhizobium species. The nodD 1 gene product from strain NGR234 was shown to determine the spectrum of compounds that induce nod-81 expression.
将NGR234 nodD 1基因以6.7 kb的HindIII片段或17 kb的XhoI片段转移到宿主范围狭窄的三叶草根瘤菌菌株ANU843中,可拓宽该细菌的宿主范围,使其包括热带豆科植物豇豆、乌苏里大豆、银合欢和大翼豆(Macroptilium atropurpureum)。与先前的数据(Bassam等人,1986年)相反,用mini-Mu lac转座子(Mu dII1734)对17 kb的XhoI片段进行诱变表明,功能性的nodD 1基因对于扩展宿主范围至关重要。使用Mu dII1734融合体和启动子克隆载体进行的基因表达研究表明,包括nodD 1基因在内的几个基因座是组成型表达的。未发现NGR234菌株nodD 1基因受其产物调控的证据。另一个基因座nod-81仅在存在包括大豆(Glycine max)在内的各种植物物种的渗出物时才被诱导。虽然nod-81的表达依赖于功能性nodD 1基因产物的存在,但使用现有的寡核苷酸杂交探针在该基因的5'端未检测到调控性的nod-box DNA序列。nod-81基因座可被新鲜发芽大豆幼苗子叶和根组织中的染料木黄酮、大豆苷元、柚皮素和香豆雌酚诱导。多种市售酚类化合物可刺激nod-81基因座的诱导,包括一些在其他根瘤菌物种中拮抗nod基因诱导的化合物。已证明NGR234菌株的nodD 1基因产物可决定诱导nod-81表达的化合物谱。