Buchmann I, Marner F J, Schröder G, Waffenschmidt S, Schröder J
Institut für Biologie II, Universität Freiburg, Schänzlestr. 1, D-7800, Freiburg, FRG.
EMBO J. 1985 Apr;4(4):853-9. doi: 10.1002/j.1460-2075.1985.tb03710.x.
Gene 4 from the T-region of Ti plasmids is responsible for cytokinin effects in crown gall cells; we investigated whether it codes for an enzyme of hormone biosynthesis. In a first set of experiments, gene 4 from octopine plasmid pTiAch5 and nopaline plasmid pTiC58 was expressed in Escherichia coli, and the gene products were identified by reaction with antiserum raised against a decapeptide derived from the DNA sequence of the gene. Extracts from cells expressing the gene contained high isopentenyl-transferase activity catalyzing the formation of N6-(delta2-isopentenyl)adenosine from 5'-AMP and delta2-isopentenylpyrophosphate. The cytokinin was identified by sequential h.p.l.c. chromatography and mass spectrometry. In a second set of experiments it was shown that crown gall cells contained isopentenyltransferase activity and a protein of mol. wt. 27 000 which was identified as the product of gene 4 by reaction with the antiserum. Isopentenyltransferase activity was specifically inhibited by the antiserum. No comparable enzyme activity or immunoreactive protein was detected in cytokinin-autotrophic, T-DNA free tobacco cells. The results establish that gene 4 from the T-region of octopine and nopaline Ti plasmids codes for an enzyme of cytokinin biosynthesis.
来自Ti质粒T区域的基因4负责冠瘿瘤细胞中的细胞分裂素效应;我们研究了它是否编码一种激素生物合成酶。在第一组实验中,章鱼碱型质粒pTiAch5和胭脂碱型质粒pTiC58中的基因4在大肠杆菌中表达,通过与针对源自该基因DNA序列的十肽产生的抗血清反应来鉴定基因产物。表达该基因的细胞提取物具有高异戊烯基转移酶活性,可催化由5'-AMP和δ2-异戊烯基焦磷酸形成N6-(δ2-异戊烯基)腺苷。通过高效液相色谱和质谱联用对细胞分裂素进行了鉴定。在第二组实验中表明,冠瘿瘤细胞含有异戊烯基转移酶活性和一种分子量为27000的蛋白质,通过与抗血清反应将其鉴定为基因4的产物。异戊烯基转移酶活性被抗血清特异性抑制。在细胞分裂素自养、无T-DNA的烟草细胞中未检测到类似的酶活性或免疫反应性蛋白。结果表明,章鱼碱型和胭脂碱型Ti质粒T区域的基因4编码一种细胞分裂素生物合成酶。