Taller B J, Murai N, Skoog F
Department of Botany, Birge Hall, University of Wisconsin, Madison, Wisconsin 53706.
Plant Physiol. 1987 Apr;83(4):755-60. doi: 10.1104/pp.83.4.755.
Endogenous cytokinin-active ribonucleosides were isolated from the rRNA and tRNA of pea epicotyls (Pisum sativum L., var Alaska) and of wheat germ (Triticum aestivum). The RNA preparations were analyzed for cytokinins by enzymic hydrolysis, ethyl acetate extraction, and Sephadex LH-20 fractionation in several solvents. Tentative identification of the cytokinins was based on cochromatography with synthetic cytokinin standards in several systems and on activity in the tobacco bioassay. Both the rRNA and tRNA from 10 day old pea epicotyls contained ribosylzeatin, isopentenyladenosine, and 2-methylthioribosylzeatin. The latter compound was the most active fraction in the pea rRNA, but was the least active fraction in the tRNA, where isopentenyladenosine activity was predominant. The 2-methylthioribosylzeatin from pea rRNA was identified by gas chromatography-mass spectrometry. Wheat germ rRNA contained cis and trans ribosylzeatin and 2-methylthioribosylzeatin. The tRNA contained isopentenyladenosine in addition. The specific cytokinin activity (activity per A(260) unit) of the tRNA was over forty times that of the rRNA. Significant contamination of the rRNA preparations by cytokinin-containing tRNA is considered unlikely on the basis of quantitative differences in the cytokinin content of the rRNA and tRNA preparations, electrophoretic analysis of rRNA purity and cytokinin analysis of fractionated oligonucleotide digests.
从豌豆上胚轴(豌豆,阿拉斯加品种)和小麦胚芽(普通小麦)的核糖体RNA(rRNA)及转运RNA(tRNA)中分离出了内源性细胞分裂素活性核糖核苷。通过酶解、乙酸乙酯萃取以及在几种溶剂中进行葡聚糖凝胶LH - 20分级分离,对RNA制剂进行细胞分裂素分析。细胞分裂素的初步鉴定基于在多个系统中与合成细胞分裂素标准品的共色谱分析以及烟草生物测定中的活性。10日龄豌豆上胚轴的rRNA和tRNA均含有核糖基玉米素、异戊烯基腺苷和2 - 甲基硫代核糖基玉米素。后一种化合物是豌豆rRNA中活性最高的组分,但在tRNA中活性最低,tRNA中异戊烯基腺苷活性占主导。通过气相色谱 - 质谱联用鉴定了豌豆rRNA中的2 - 甲基硫代核糖基玉米素。小麦胚芽rRNA含有顺式和反式核糖基玉米素以及2 - 甲基硫代核糖基玉米素。tRNA还含有异戊烯基腺苷。tRNA的比细胞分裂素活性(每A(260)单位的活性)是rRNA的四十多倍。基于rRNA和tRNA制剂中细胞分裂素含量的定量差异、rRNA纯度的电泳分析以及分级寡核苷酸消化产物的细胞分裂素分析,认为rRNA制剂不太可能被含细胞分裂素的tRNA显著污染。