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组成型表达胡芦巴半乳甘露聚糖半乳糖基转移酶的烟草转基因株系,其种子胚乳细胞壁中的半乳甘露聚糖结构发生了改变。

Tobacco transgenic lines that express fenugreek galactomannan galactosyltransferase constitutively have structurally altered galactomannans in their seed endosperm cell walls.

作者信息

Reid J S Grant, Edwards Mary E, Dickson Cathryn A, Scott Catherine, Gidley Michael J

机构信息

Department of Biological Sciences, University of Stirling, Stirling FK9 4LA, United Kingdom.

出版信息

Plant Physiol. 2003 Mar;131(3):1487-95. doi: 10.1104/pp.102.016840.

Abstract

Galactomannans [(1-->6)-alpha-D-galactose (Gal)-substituted (1-->4)-beta-D-mannans] are major cell wall storage polysaccharides in the endosperms of some seeds, notably the legumes. Their biosynthesis in developing legume seeds involves the functional interaction of two membrane-bound glycosyltransferases, mannan synthase (MS) and galactomannan galactosyltransferase (GMGT). MS catalyzes the elongation of the mannan backbone, whereas GMGT action determines the distribution and amount of Gal substitution. Fenugreek (Trigonella foenum-graecum) forms a galactomannan with a very high degree of Gal substitution (Man/Gal = 1.1), and its GMGT has been characterized. We now report that the endosperm cell walls of the tobacco (Nicotiana tabacum) seed are rich in a galactomannan with a very low degree of Gal substitution (Man/Gal about 20) and that its depositional time course is closely correlated with membrane-bound MS and GMGT activities. Furthermore, we demonstrate that seeds from transgenic tobacco lines that express fenugreek GMGT constitutively in membrane-bound form have endosperm galactomannans with increased average degrees of Gal substitution (Man/Gal about 10 in T(1) generation seeds and about 7.5 in T(2) generation seeds). Membrane-bound enzyme systems from transgenic seed endosperms form galactomannans in vitro that are more highly Gal substituted than those formed by controls under identical conditions. To our knowledge, this is the first report of structural manipulation of a plant cell wall polysaccharide in transgenic plants via a biosynthetic membrane-bound glycosyltransferase.

摘要

半乳甘露聚糖[(1→6)-α-D-半乳糖(Gal)取代的(1→4)-β-D-甘露聚糖]是一些种子胚乳中的主要细胞壁储存多糖,尤其是豆科植物。它们在发育中的豆科植物种子中的生物合成涉及两种膜结合糖基转移酶,甘露聚糖合酶(MS)和半乳甘露聚糖半乳糖基转移酶(GMGT)的功能相互作用。MS催化甘露聚糖主链的延长,而GMGT的作用决定了Gal取代的分布和数量。胡芦巴(Trigonella foenum-graecum)形成一种具有非常高Gal取代度(Man/Gal = 1.1)的半乳甘露聚糖,并且其GMGT已得到表征。我们现在报告,烟草(Nicotiana tabacum)种子的胚乳细胞壁富含一种具有非常低Gal取代度(Man/Gal约为20)的半乳甘露聚糖,并且其沉积时间进程与膜结合的MS和GMGT活性密切相关。此外,我们证明,来自在膜结合形式下组成性表达胡芦巴GMGT的转基因烟草品系的种子,其胚乳半乳甘露聚糖的平均Gal取代度增加(T1代种子中Man/Gal约为10,T2代种子中约为7.5)。来自转基因种子胚乳的膜结合酶系统在体外形成的半乳甘露聚糖比相同条件下对照形成的半乳甘露聚糖具有更高的Gal取代度。据我们所知,这是通过生物合成膜结合糖基转移酶对转基因植物中植物细胞壁多糖进行结构操纵的首次报道。

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