Leyva A, Palacios J M, Mozo T, Ruiz-Argüeso T
Departamento de Microbiología, Universidad Politécnica, Madrid, Spain.
J Bacteriol. 1987 Nov;169(11):4929-34. doi: 10.1128/jb.169.11.4929-4934.1987.
A gene library of genomic DNA from the hydrogen uptake (Hup)-positive strain 128C53 of Rhizobium leguminosarum was constructed by using the broad-host-range mobilizable cosmid vector pLAFR1. The resulting recombinant cosmids contained insert DNA averaging 21 kilobase pairs (kb) in length. Two clones from the above gene library were identified by colony hybridization with DNA sequences from plasmid pHU1 containing hup genes of Bradyhizobium japonicum. The corresponding recombinant cosmids, pAL618 and pAL704, were isolated, and a region of about 28 kb containing the sequences homologous to B. japonicum hup-specific DNA was physically mapped. Further hybridization analysis with three fragments from pHU1 (5.9-kb HindIII, 2.9-kb EcoRI, and 5.0-kb EcoRI) showed that the overall arrangement of the R. leguminosarum hup-specific region closely parallels that of B. japonicum. The presence of functional hup genes within the isolated cosmid DNA was demonstrated by site-directed Tn5 mutagenesis of the 128C53 genome and analysis of the Hup phenotype of the Tn5 insertion strains in symbiosis with peas. Transposon Tn5 insertions at six different sites spanning 11 kb of pAL618 completely suppressed the hydrogenase activity of the pea bacteroids.
利用广宿主范围可移动黏粒载体pLAFR1构建了豆科根瘤菌吸氢(Hup)阳性菌株128C53的基因组DNA基因文库。所得重组黏粒所含插入DNA平均长度为21千碱基对(kb)。通过与含有日本慢生根瘤菌hup基因的质粒pHU1的DNA序列进行菌落杂交,从上述基因文库中鉴定出两个克隆。分离出相应的重组黏粒pAL618和pAL704,并对包含与日本慢生根瘤菌hup特异性DNA同源序列的约28 kb区域进行了物理图谱分析。用pHU1的三个片段(5.9-kb HindIII、2.9-kb EcoRI和5.0-kb EcoRI)进行进一步杂交分析表明,豆科根瘤菌hup特异性区域的总体排列与日本慢生根瘤菌的非常相似。通过对128C53基因组进行定点Tn5诱变以及分析Tn5插入菌株与豌豆共生时的Hup表型,证明了分离出的黏粒DNA中存在功能性hup基因。转座子Tn5在跨越pAL618 11 kb的六个不同位点插入,完全抑制了豌豆类菌体的氢化酶活性。