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Identification and Partial Characterization of the Pectin Methyltransferase Homogalacturonan-Methyltransferase from Membranes of Tobacco Cell Suspensions

机译:果胶的鉴定和部分表征 来自的甲基转移酶同型半乳糖醛酸-甲基转移酶 烟草悬浮液膜

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摘要

A membrane preparation from tobacco (Nicotiana tabacum L.) cells contains at least one enzyme that is capable of transferring the methyl group from S-adenosyl-methionine (SAM) to the C6 carboxyl of homogalacturonan present in the membranes. This enzyme is named homogalacturonan-methyltransferase (HGA-MT) to distinguish it from methyltransferases that catalyze methyletherification of the pectic polysaccharides rhamnogalacturonan I or rhamnogalacturonan II. A trichloroacetic acid precipitation assay was used to measure HGA-MT activity, because published procedures to recover pectic polysaccharides via ethanol or chloroform:methanol precipitation lead to high and variable background radioactivity in the product pellet. Attempts to reduce the incorporation of the 14C-methyl group from SAM into pectin by the addition of the alternative methyl donor 5-methyltetrahydrofolate were unsuccessful, supporting the role of SAM as the authentic methyl donor for HGA-MT. The pH optimum for HGA-MT in membranes was 7.8, the apparent Michaelis constant for SAM was 38 μm, and the maximum initial velocity was 0.81 pkat mg−1 protein. At least 59% of the radiolabeled product was judged to be methylesterified homogalacturonan, based on the release of radioactivity from the product after a mild base treatment and via enzymatic hydrolysis by a purified pectin methylesterase. The released radioactivity eluted with a retention time identical to that of methanol upon fractionation over an organic acid column. Cleavage of the radiolabeled product by endopolygalacturonase into fragments that migrated as small oligomers of HGA during thin-layer chromatography, and the fact that HGA-MT activity in the membranes is stimulated by uridine 5′-diphosphate galacturonic acid, a substrate for HGA synthesis, confirms that the bulk of the product recovered from tobacco membranes incubated with SAM is methylesterified HGA.
机译:来自烟草(Nicotiana tabacum L.)细胞的膜制剂包含至少一种酶,该酶能够将甲基从S-腺苷甲硫氨酸(SAM)转移至膜中存在的高半乳糖醛酸的C6羧基。该酶称为高半乳糖醛酸聚糖甲基转移酶(HGA-MT),以区别于催化果胶多糖鼠李糖半乳糖醛酸聚糖I或鼠李糖半乳糖醛酸聚糖II的甲基醚化的甲基转移酶。使用三氯乙酸沉淀测定法来测量HGA-MT活性,因为已公开的通过乙醇或氯仿:甲醇沉淀回收果胶多糖的程序会导致产品沉淀物中高且可变的背景放射性。尝试通过添加替代的甲基供体5-甲基四氢叶酸来减少SAM中的 14 C-甲基基团并入果胶的尝试未能成功,这支持了SAM作为HGA-的真正甲基供体的作用。公吨。膜中HGA-MT的最适pH为7.8,SAM的表观米氏常数 为38μm,最大初始速度为0.81 pkat mg -1 蛋白。至少有59%的放射性标记产品 被认为是甲基化的高半乳糖醛酸 轻度碱处理后产品释放出的放射性 并通过纯化的果胶甲基酯酶进行酶促水解。的 释放的放射性以与保留时间相同的保留时间洗脱 在有机酸柱上分馏得到甲醇。分裂 内聚半乳糖醛酸酶将放射性标记的产物转化为 薄层中迁移为HGA的小寡聚体的片段 层析,以及膜中HGA-MT活性是 受尿苷5'-二磷酸半乳糖醛酸(一种底物)刺激 HGA合成证实了从中回收的大部分产品 与SAM一起孵育的烟草膜是甲基酯化的HGA。

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