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吲哚-3-基乙酰基-肌醇半乳糖苷的酶促合成

Enzymic synthesis of indol-3-ylacetyl-myo-inositol galactoside.

作者信息

Corcuera L J, Michalczuk L, Bandurski R S

出版信息

Biochem J. 1982 Nov 1;207(2):283-90. doi: 10.1042/bj2070283.

DOI:10.1042/bj2070283
PMID:7159382
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1153858/
Abstract

Extracts of immature kernels of Zea mays catalysed the synthesis of indol-3-ylacetyl-myo-inositol galactoside from indol-3-ylacetyl-myo-inositol and UDP-galactose. Addition of 2-mercaptoethanol was required for stability of the catalytic activity during dialysis. The enzyme could be fractionated with (NH4)2SO4, and 55% of the activity was recovered in the 30-60%-saturation fraction. The product of the reaction contained radioactivity from UDP-[U-14C]galactose and was identified as indol-3-ylacetyl-myo-inositol galactoside by gas chromatography-mass spectrometry. Therefore a UDP-galactose:indol-3-ylacetyl-myo-inositol galactosyltransferase (indol-3-ylacetyl-myo-inositol galactoside synthase) is present in developing kernels of Zea mays. The description of this enzyme, together with the enzymes described in the accompanying paper [Michalczuk & Bandurski (1982) Biochem. J. 207, 273-281] for the synthesis of indol-3-ylacetylglucose and indol-3-ylacetyl-myo-inositol, now provides mechanisms for the biosynthesis of one-half of the low-molecular-weight esters of indol-3-ylacetic acid in Zea mays.

摘要

玉米未成熟籽粒的提取物催化了吲哚 - 3 - 基乙酰 - 肌醇半乳糖苷从吲哚 - 3 - 基乙酰 - 肌醇和UDP - 半乳糖的合成。透析过程中,为保持催化活性的稳定性需要添加2 - 巯基乙醇。该酶可用硫酸铵分级分离,55%的活性在饱和度为30% - 60%的级分中得以回收。反应产物含有来自UDP - [U - 14C]半乳糖的放射性,通过气相色谱 - 质谱法鉴定为吲哚 - 3 - 基乙酰 - 肌醇半乳糖苷。因此,在玉米发育中的籽粒中存在一种UDP - 半乳糖:吲哚 - 3 - 基乙酰 - 肌醇半乳糖基转移酶(吲哚 - 3 - 基乙酰 - 肌醇半乳糖苷合酶)。对该酶的描述,连同随附论文[Michalczuk & Bandurski (1982) Biochem. J. 207, 273 - 281]中描述的用于合成吲哚 - 3 - 基乙酰葡萄糖和吲哚 - 3 - 基乙酰 - 肌醇的酶,现在为玉米中吲哚 - 3 - 基乙酸低分子量酯一半的生物合成提供了机制。

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本文引用的文献

1
Myo-Inositol Esters of Indole-3-acetic Acid as Seed Auxin Precursors of Zea mays L.吲哚 - 3 - 乙酸的肌醇酯作为玉米的种子生长素前体
Plant Physiol. 1980 Mar;65(3):422-7. doi: 10.1104/pp.65.3.422.
2
Concentration and Metabolic Turnover of Indoles in Germinating Kernels of Zea mays L.玉米发芽种子中吲哚的浓度和代谢周转率
Plant Physiol. 1980 Mar;65(3):415-21. doi: 10.1104/pp.65.3.415.
3
Purification and Partial Characterization of a Glucan Containing Indole-3-acetic Acid.含吲哚-3-乙酸葡聚糖的纯化和部分特性分析。
Plant Physiol. 1972 Jul;50(1):176-82. doi: 10.1104/pp.50.1.176.
4
Gas-Liquid Chromatographic Analysis of Indole-3-acetic Acid Myoinositol Esters in Maize Kernels.玉米胚乳中吲哚-3-乙酸肌醇酯的气液色谱分析。
Plant Physiol. 1970 Nov;46(5):715-9. doi: 10.1104/pp.46.5.715.
5
Biosynthesis of Stachyose in Phaseolus vulgaris.菜豆中水苏糖的生物合成
Plant Physiol. 1966 Nov;41(9):1540-2. doi: 10.1104/pp.41.9.1540.
6
Synthesis of galactosylinositol by extracts from peas.豌豆提取物合成半乳糖基肌醇。
Biochem Biophys Res Commun. 1963 Jul 18;12:121-5. doi: 10.1016/0006-291x(63)90246-8.
7
Metabolic conversion of 14C-indole-3-acetic acid to 14C-oxindole-3-acetic acid.14C-吲哚-3-乙酸向14C-氧化吲哚-3-乙酸的代谢转化。
Biochem Biophys Res Commun. 1981 Nov 30;103(2):429-33. doi: 10.1016/0006-291x(81)90470-8.
8
UDP-glucose: indoleacetic acid glucosyl transferase and indoleacetyl-glucose: myo-inositol indoleacetyl transferase.UDP-葡萄糖:吲哚乙酸葡萄糖基转移酶和吲哚乙酰葡萄糖:肌醇吲哚乙酰转移酶
Biochem Biophys Res Commun. 1980 Mar 28;93(2):588-92. doi: 10.1016/0006-291x(80)91118-3.
9
Enzymic synthesis of 1-O-indol-3-ylacetyl-beta-D-glucose and indol-3-ylacetyl-myo-inositol.1-O-吲哚-3-基乙酰基-β-D-葡萄糖和吲哚-3-基乙酰基-肌醇的酶促合成
Biochem J. 1982 Nov 1;207(2):273-81. doi: 10.1042/bj2070273.
10
A partial characterization of indoleacetylinositols from ZEA mays.来自玉米的吲哚乙酰肌醇的部分特性分析。
Biochem Biophys Res Commun. 1965 Sep 8;20(5):641-6. doi: 10.1016/0006-291x(65)90448-1.