Co-ordinated synthesis of gentiobiitol and sorbitol, evidence of sorbitol glycosylation in transgenic sugarcane

被引:11
作者
Chong, Barrie Fong [1 ,4 ]
Abeydeera, W. P. P. [3 ,4 ]
Glassop, Donna [2 ,4 ]
Bonnett, Graham D. [2 ,4 ]
O'Shea, Michael G. [1 ,4 ]
Brumbley, Stevens M. [4 ,5 ]
机构
[1] BSES Ltd, David N Plant Res Ctr, Indooroopilly, Qld 4068, Australia
[2] CSIRO, Plant Ind, Queensland Biosci Precinct, St Lucia, Qld 4067, Australia
[3] Univ Queensland, Sch Chem Engn, St Lucia, Qld 4072, Australia
[4] Univ Queensland, Cooperat Res Ctr Sugar Ind Innovat Biotechnol, St Lucia, Qld 4072, Australia
[5] Univ Queensland, Australian Inst Bioengn & Nanotechnol, St Lucia, Qld 4072, Australia
关键词
Saccharum spp; Gramineae; 6-O-beta-D-glucopyranosyl-D-glucitol; Gentiobiitol; Sorbitol; Metabolite profiling; Sugar alcohol; ASSIGNMENT; ALCOHOLS; SIGNALS;
D O I
10.1016/j.phytochem.2010.01.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sugarcane (a Saccharum spp. interspecific hybrid) was previously engineered to synthesize sorbitol (designated as sorbitolcane). Motivated by the atypical development of the leaves in some sorbitolcane, the polar metabolite profiles in the leaves of those plants were compared against a group of control sugarcane plants. Eighty-six polar metabolites were detected in leaf extracts by GC-MS. Principal component analysis of the metabolites indicated that three compounds were strongly associated with sorbitolcane. Two were identified as sorbitol and gentiobiose and the third was unknown. Gentiobiose and the unknown compound were positively correlated with sorbitol accumulation. The unknown compound was only abundant in sorbitolcane. This compound was structurally characterized and found to be a sorbitol-glucose conjugate. C-13 NMR analysis indicated that the glucopyranose and glucitol moieties were 1,6-linked. Ligand exchange chromatography confirmed that the compound was a beta-anomer, thus identifying the compound as 6-O-beta-D-glucopyranosyl-D-glucitol, or gentiobiitol. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:736 / 741
页数:6
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