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1
Sink metabolism in tomato fruit : I. Developmental changes in carbohydrate metabolizing enzymes.番茄果实中的库代谢:I. 碳水化合物代谢酶的发育变化
Plant Physiol. 1988 Jul;87(3):727-30. doi: 10.1104/pp.87.3.727.
2
A novel sucrose synthase pathway for sucrose degradation in cultured sycamore cells.一种用于悬浮培养的梧桐细胞中蔗糖降解的新型蔗糖合酶途径。
Plant Physiol. 1986 Aug;81(4):1008-13. doi: 10.1104/pp.81.4.1008.
3
Amylopectin degradation in pea chloroplast extracts.豌豆叶绿体提取物中支链淀粉的降解。
Plant Physiol. 1978 Feb;61(2):218-20. doi: 10.1104/pp.61.2.218.
4
Concentration and metabolic turnover of UDP-glucose in developing cotton fibers.发育中棉纤维中UDP-葡萄糖的浓度与代谢周转
J Biol Chem. 1981 Jan 10;256(1):308-15.
5
Induction by growth factors of polysaccharide synthases in bean cell suspension cultures.生长因子对菜豆细胞悬浮培养物中多糖合酶的诱导作用。
Biochem J. 1983 Feb 15;210(2):509-15. doi: 10.1042/bj2100509.
6
Arabinan synthase and xylan synthase activities of Phaseolus vulgaris. Subcellular localization and possible mechanism of action.菜豆阿拉伯聚糖合酶和木聚糖合酶活性。亚细胞定位及可能的作用机制。
Biochem J. 1983 Feb 15;210(2):497-507. doi: 10.1042/bj2100497.
7
Cooperative action of beta-glucan synthetase and UDP-xylose xylosyl transferase of Golgi membranes in the synthesis of xyloglucan-like polysaccharide.高尔基体膜中β-葡聚糖合成酶与UDP-木糖木糖基转移酶在木葡聚糖样多糖合成中的协同作用。
Biochim Biophys Acta. 1980 May 22;629(3):431-44. doi: 10.1016/0304-4165(80)90149-x.
8
Metabolic changes in elicitor-treated bean cells. Enzymic responses associated with rapid changes in cell wall components.激发子处理的菜豆细胞中的代谢变化。与细胞壁成分快速变化相关的酶促反应。
Eur J Biochem. 1985 May 2;148(3):571-8. doi: 10.1111/j.1432-1033.1985.tb08878.x.
9
Elicitor- and wound-induced oxidative cross-linking of a proline-rich plant cell wall protein: a novel, rapid defense response.激发子和伤口诱导的富含脯氨酸的植物细胞壁蛋白的氧化交联:一种新型快速防御反应。
Cell. 1992 Jul 10;70(1):21-30. doi: 10.1016/0092-8674(92)90530-p.
10
Partial purification of Golgi-bound arabinosyltransferase and two isoforms of xylosyltransferase from French bean (Phaseolus vulgaris L.).从菜豆(Phaseolus vulgaris L.)中对高尔基体结合的阿拉伯糖基转移酶和木糖基转移酶的两种同工型进行部分纯化。
Biochem J. 1992 Dec 15;288 ( Pt 3)(Pt 3):817-22. doi: 10.1042/bj2880817.

菜豆(Phaseolus vulgaris L.)激发子胁迫细胞中细胞壁多糖的生物合成及相关代谢

Cell wall polysaccharide biosynthesis and related metabolism in elicitor-stressed cells of French bean (Phaseolus vulgaris L.).

作者信息

Robertson D, McCormack B A, Bolwell G P

机构信息

Department of Biochemistry, Royal Holloway and Bedford New College, University of London, Egham, Surrey, U.K.

出版信息

Biochem J. 1995 Mar 15;306 ( Pt 3)(Pt 3):745-50. doi: 10.1042/bj3060745.

DOI:10.1042/bj3060745
PMID:7702569
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1136584/
Abstract

Enzyme activities involved in quantitative and qualitative flux of sugars into cell wall polysaccharides were determined following elicitor treatment of suspension cultured cells of French bean (Phaseolus vulgaris L.). Two subsets of activities were examined: the first were involved in synthesis and metabolism of UDP-glucose and the provision of the pool of UDP-sugars, and the second a selection of membrane-bound glycosyltransferases involved in the synthesis of pectins, hemicelluloses and glucans of the primary cell wall. Of the first group, only UDP-glucose dehydrogenase (EC 1.1.1.22) showed any significant induction in response to elicitor treatment, sucrose synthase (EC 2.4.1.13), UDP-glucuronate decarboxylase (EC 4.1.1.35), UDP-glucose and UDP-xylose 4-epimerases (EC 5.1.3.2 and EC 5.1.3.5 respectively) did not change in activity significantly over the time course. In contrast, enzymes of the second group showed a more complex response. Callose synthase (glucan synthase II, EC 2.4.1.12) increased in activity, as has been shown in other systems, while arabinan synthase (EC 2.4.1.-), xylan synthase (EC 2.4.1.72), xyloglucan synthase (EC 2.4.1.72) and glucan synthase I (EC 2.4.1.12) activities were rapidly depleted from membranes within 3 h following elicitor action. This rapid turnover of activity was striking, indicating that the half-life of such enzymes can be short and that elicitor action causes substantial perturbation of some membrane activities. Glucan synthase I activity appears to increase in the later stages over the time period measured, indicating some recovery of this metabolism.

摘要

在用激发子处理菜豆(Phaseolus vulgaris L.)悬浮培养细胞后,测定了参与糖类定量和定性流入细胞壁多糖过程的酶活性。研究了两组酶活性:第一组参与UDP - 葡萄糖的合成与代谢以及UDP - 糖库的供应,第二组是参与初生细胞壁果胶、半纤维素和葡聚糖合成的一些膜结合糖基转移酶。在第一组中,只有UDP - 葡萄糖脱氢酶(EC 1.1.1.22)在激发子处理后表现出显著诱导,蔗糖合酶(EC 2.4.1.13)、UDP - 葡萄糖醛酸脱羧酶(EC 4.1.1.35)、UDP - 葡萄糖和UDP - 木糖4 - 表异构酶(分别为EC 5.1.3.2和EC 5.1.3.5)在整个时间进程中活性没有显著变化。相比之下,第二组酶表现出更复杂的反应。正如在其他系统中所显示的,胼胝质合酶(葡聚糖合酶II,EC 2.4.1.12)活性增加,而阿拉伯聚糖合酶(EC 2.4.1.-)、木聚糖合酶(EC 2.4.1.72)、木葡聚糖合酶(EC 2.4.1.72)和葡聚糖合酶I(EC 2.4.1.12)的活性在激发子作用后3小时内迅速从膜上消失。这种活性的快速转换很显著,表明这些酶的半衰期可能很短,并且激发子作用会对一些膜活性造成实质性干扰。在所测量的时间段后期,葡聚糖合酶I活性似乎增加,表明这种代谢有一定程度的恢复。