Paulus F, Otten L
CNRS Plant Molecular Biology Laboratory, Strasbourg, France.
Mol Plant Microbe Interact. 1993 May-Jun;6(3):393-402. doi: 10.1094/mpmi-6-393.
Agrocinopine synthase genes have so far been detected only on the Agrobacterium tumefaciens nopaline Ti plasmid pTiC58 and on the A. rhizogenes Ri plasmid pRiA4. The TA region of the octopine/cucumopine (o/c) A. vitis Ti plasmid pTiTm4 strongly resembles the TL DNA of biotype I octopine Ti plasmids. In addition, it carries an intact and functional agrocinopine synthase gene close to its left border. TA/TL sequence comparison shows that the biotype I TL region still carries a 5'-deleted acs gene, strongly indicating that this gene was originally part of the TL region and belongs to the "common DNA" region of octopine and nopaline Ti plasmids. Tm4 and C58C1 (pTiTm4) remove agrocinopine A from the medium indicating that pTiTm4 also carries agrocinopine uptake genes. In spite of this, Tm4 and related strains are resistant against agrocin 84. Two o/c Ti plasmids that are closely related to pTiTm4, pTiHm1, and pTiAB3, have a mutated acs gene; whereas Hm1 can still take up agrocinopine A, AB3 cannot. These results yield new insights in the evolution of octopine, nopaline, and o/c strains.
到目前为止,农杆碱合成酶基因仅在根癌农杆菌胭脂碱型Ti质粒pTiC58和发根农杆菌Ri质粒pRiA4上被检测到。葡萄土壤杆菌的章鱼碱/黄瓜碱(o/c)型Ti质粒pTiTm4的TA区域与生物I型章鱼碱Ti质粒的TL DNA非常相似。此外,它在其左边界附近携带一个完整且有功能的农杆碱合成酶基因。TA/TL序列比较表明,生物I型TL区域仍然携带一个5'端缺失的acs基因,这强烈表明该基因最初是TL区域的一部分,属于章鱼碱和胭脂碱型Ti质粒的“共同DNA”区域。Tm4和C58C1(pTiTm4)能从培养基中去除农杆碱A,这表明pTiTm4也携带农杆碱摄取基因。尽管如此,Tm4及相关菌株对农杆菌素84具有抗性。与pTiTm4密切相关的两个o/c Ti质粒pTiHm1和pTiAB3,有一个突变的acs基因;而Hm1仍然可以摄取农杆碱A,AB3则不能。这些结果为章鱼碱型、胭脂碱型和o/c型菌株的进化提供了新的见解。