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软腐欧文氏菌属及从马铃薯块茎中分离出的其他果胶分解细菌在果胶酸解聚过程中的电导响应分析。

Analysis of conductance responses during depolymerization of pectate by soft rot Erwinia spp. and other pectolytic bacteria isolated from potato tubers.

作者信息

Fraaije B A, Bosveld M, Van den Bulk R W, Rombouts F M

机构信息

DLO-Centre for Plant Breeding and Reproduction Research (CPRO-DLO), Wageningen, The Netherlands.

出版信息

J Appl Microbiol. 1997 Jul;83(1):17-24. doi: 10.1046/j.1365-2672.1997.d01-396.x.

Abstract

Different bacteria isolated from potato tubers were screened for their pectolytic properties by examining pitting in polypectate agar, recording conductance responses in polypectate medium and performing potato tuber soft rot tests. For bacteria found positive in conductimetry, the role of polygalacturonase (PG) and pectate lyase (PL) in the generation of conductance changes in a polygalacturonic acid (PGA) medium was further analysed using enzyme activity staining after gel electrophoresis and high-performance anion exchange chromatography. The extent of the conductance changes during depolymerization of PGA was dependent on the amounts of galacturonate monomers and oligomers accumulated in the medium. In comparison with an unidentified saprophyte and a Klebsiella strain, both mainly having PL activity, soft rot Erwinia spp. rapidly produced larger conductance responses, due to a combined action of multiple forms of PG and PL. The responses of Erwinia spp. were initially associated with the accumulation of large amounts of monomers and saturated dimers to heptamers, due to PG activity. Subsequently, as well as monomers and saturated dimers, large amounts of unsaturated dimers were also detected, due to PL activity. The role of PG as an important conductimetric factor was also demonstrated for a pectinase preparation derived from Aspergillus niger. Besides detection, automated conductimetric assays in pectate media may also be useful for monitoring of pectolytic activity in pectinase preparations and for screening of pectolytic activity of microorganisms under different media and growth conditions.

摘要

通过检测在聚果胶酸盐琼脂中的蚀斑、记录在聚果胶酸盐培养基中的电导响应以及进行马铃薯块茎软腐试验,对从马铃薯块茎中分离出的不同细菌的果胶分解特性进行了筛选。对于在电导测定中呈阳性的细菌,使用凝胶电泳和高效阴离子交换色谱后的酶活性染色,进一步分析了聚半乳糖醛酸酶(PG)和果胶酸裂解酶(PL)在聚半乳糖醛酸(PGA)培养基中产生电导变化的作用。PGA解聚过程中电导变化的程度取决于培养基中积累的半乳糖醛酸单体和寡聚物的量。与一种未鉴定的腐生菌和一株主要具有PL活性的克雷伯氏菌菌株相比,软腐欧文氏菌属由于多种形式的PG和PL的联合作用,能迅速产生更大的电导响应。欧文氏菌属的响应最初与由于PG活性导致的大量单体以及饱和二聚体至七聚体的积累有关。随后,由于PL活性,除了单体和饱和二聚体外,还检测到大量不饱和二聚体。对于源自黑曲霉的果胶酶制剂,PG作为一个重要的电导因子的作用也得到了证明。除了检测之外,在果胶酸盐培养基中的自动电导测定对于监测果胶酶制剂中的果胶分解活性以及筛选不同培养基和生长条件下微生物的果胶分解活性也可能是有用的。

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