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短小芽孢杆菌聚半乳糖醛酸转消除酶产生的低聚寡糖醛酸的制备、分离及降解

Preparation, separation and degradation of oligouronides produced by the polygalacturonic acid transeliminase of Bacillus pumilus.

作者信息

Davé B A, Vaughn R H, Patel I B

出版信息

J Chromatogr. 1976 Jan 21;116(2):395-405. doi: 10.1016/s0021-9673(00)89909-4.

Abstract

Production of the end products of polygalacturonic acid degradation on a large scale was done by reacting free galacturonic acid with Bacillus pumilus polygalacturonic acid transeliminase (PATE, EC 4.2.2.2) to obtain a mixture of the barium salts of several oligouronides. Small amounts of the unsaturated oligouronides were separated by paper chromatography. Large quantities of unsaturated oligouronides were separated on a AG-1-X8 (formate) column by applying a sample of mixed oligouronides and stepwise elution was carried out with sodium formate buffer (pH 4.7). The unsaturated oligouronides were identified on the basis of chromatographic mobilities, Sephadex gel filtration data, COOH/CHO ratio, thiobarbituric acid-reacting material, bromine uptake, and chemical and enzymatic degradation data as unsaturated tri-, tetra-, and hexagalacturonic acids. The chemical degradation of these unsaturated oligouronides, done with 6 N HCl by heating at 100 degrees for 30 min, gave qualitatively identical products of hydrolysis. These products compared with authentic standards, were identified as galacturonic acid, formic acid, 5-formyl-2-furancarboxylic acid, and 2-furancarboxylic acid. Analysis of the enzymatic breakdown products of the higher unsaturated uronides showed that a minimum of four galacturonic acid units was required for the action of purified endo-PATE from B. pumilus. The unsaturated trimer was not attacked, thus accounting for its accumulation as the major end product of polygalacturonate degradation by this enzyme.

摘要

通过使游离半乳糖醛酸与短小芽孢杆菌聚半乳糖醛酸转消除酶(PATE,EC 4.2.2.2)反应,大规模生产聚半乳糖醛酸降解的终产物,以获得几种低聚半乳糖醛酸钡盐的混合物。少量不饱和低聚半乳糖醛酸通过纸色谱法分离。通过应用混合低聚半乳糖醛酸样品,在AG-1-X8(甲酸盐)柱上分离大量不饱和低聚半乳糖醛酸,并用甲酸钠缓冲液(pH 4.7)进行分步洗脱。根据色谱迁移率、葡聚糖凝胶过滤数据、COOH/CHO比值、硫代巴比妥酸反应物质、溴吸收以及化学和酶促降解数据,将不饱和低聚半乳糖醛酸鉴定为不饱和三、四和六聚半乳糖醛酸。这些不饱和低聚半乳糖醛酸用6 N HCl在100℃加热30分钟进行化学降解,得到定性相同的水解产物。与标准品相比,这些产物被鉴定为半乳糖醛酸、甲酸、5-甲酰基-2-呋喃羧酸和2-呋喃羧酸。对较高不饱和糖醛酸酯的酶促分解产物的分析表明,短小芽孢杆菌纯化的内切PATE发挥作用至少需要四个半乳糖醛酸单元。不饱和三聚体未被攻击,因此解释了其作为该酶降解聚半乳糖醛酸的主要终产物而积累的原因。

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