首页> 外文期刊>Journal of Experimental Botany >Molecular and functional characterization of a cDNA encoding fructan:fructan 6G-fructosyltransferase (6G-FFT)/fructan:fructan 1-fructosyltransferase (1-FFT) from perennial ryegrass (Lolium perenne L.)
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Molecular and functional characterization of a cDNA encoding fructan:fructan 6G-fructosyltransferase (6G-FFT)/fructan:fructan 1-fructosyltransferase (1-FFT) from perennial ryegrass (Lolium perenne L.)

机译:多年生黑麦草(Lolium perenne L.)

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摘要

Fructans are the main storage compound in Lolium perenne. To account for the prevailing neokestose-based fructan synthesis in this species, a cDNA library of L. perenne was screened by using the onion (Allium cepa) fructan:fructan 6G-fructosyltransferase (6G-FFT) as a probe. A full length Lp6G-FFT clone was isolated with significant homologies to vacuolar type fructosyltransferases and invertases. The functionality of the cDNA was tested by heterologous expression in Pichia pastoris. The recombinant protein demonstrated both 6G-FFT and fructan:fructan 1-fructosyltransferase activities (1-FFT) with a maximum 6G-FFT/1-FFT ratio of two. The activity of 6G-FFT was investigated with respect to developmental stage, tissue distribution, and alterations in carbohydrate status expression and compared to sucrose:sucrose 1-fructosyltransferase (1-SST). Lp6G-FFT and Lp1-SST were predominantly expressed in the basal part of elongating leaves and leaf sheaths. Expression of both genes declined along the leaf axis, in parallel with the spatial occurrence of fructan and fructosyltransferase activities. Surprisingly, Lp6G-FFT was highly expressed in photosynthetically active tissues where very low extractable fructosyltransferase activity and fructan amounts were detected, suggesting a post-transcriptional regulation of expression. Lp6G-FFT gene expression increased only in elongating leaves following similar increases of sucrose content in blades, sheaths, and elongating leaf bases. Regulation of Lp6G-FFT gene expression depends on the tissue according to its sink–source status.
机译:果糖是黑麦草中的主要储存化合物。为了说明该物种中普遍存在的基于新核糖的果聚糖合成,使用洋葱(洋葱)果聚糖:果聚糖6G-果糖基转移酶(6G-FFT)作为探针筛选了紫苏乳酸杆菌的cDNA文库。分离出全长Lp6G-FFT克隆,与液泡型果糖基转移酶和转化酶具有显着同源性。通过在毕赤酵母中的异源表达来测试cDNA的功能。重组蛋白同时具有6G-FFT和果糖:果糖1-果糖基转移酶活性(1-FFT),最大6G-FFT / 1-FFT比率为2。研究了6G-FFT的活性,涉及发育阶段,组织分布和碳水化合物状态表达的变化,并与蔗糖:蔗糖1-果糖基转移酶(1-SST)进行了比较。 Lp6G-FFT和Lp1-SST主要在伸长的叶和叶鞘的基部表达。两种基因的表达沿叶轴下降,与果聚糖和果糖基转移酶活性的空间发生平行。出人意料的是,Lp6G-FFT在光合活性组织中高表达,在那里检测到非常低的可提取果糖基转移酶活性和果聚糖含量,表明转录后表达调控。 Lp6G-FFT基因表达仅在叶片,鞘和叶片基部中蔗糖含量的相似增加之后才在叶片中增加。 Lp6G-FFT基因表达的调节取决于其汇源状态的组织。

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