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在优化条件下,通过米曲霉固态培养从农业和农工业残渣中高效生产多聚半乳糖醛酸酶。

Efficient polygalacturonase production from agricultural and agro-industrial residues by solid-state culture of Aspergillus sojae under optimized conditions.

作者信息

Heerd Doreen, Diercks-Horn Sonja, Fernández-Lahore Marcelo

机构信息

Downstream Processing Laboratory, Jacobs University Bremen gGmbH, Campus Ring 1, 28759 Bremen, Germany.

出版信息

Springerplus. 2014 Dec 16;3:742. doi: 10.1186/2193-1801-3-742. eCollection 2014.

Abstract

Previously identified fungal pectinase producers of the species Aspergillus sojae were used for optimization of polygalacturonase production in solid-state fermentation applying Design of Experiment. The effects of media composition and several process parameters, like inoculum size, moisture level, incubation time and temperature on polygalacturonase activity were studied in screening and optimization investigations. Utilization of agricultural and agro-industrial by-products provided the establishment of a cost-efficient and sustainable process for enzyme production. Comparison of pectinase production by A. sojae ATCC 20235 and A. sojae CBS 100928 under optimized conditions yielded 6.9 times higher polygalacturonase activity by A. sojae ATCC 20235. Highest enzyme yield (909.5 ± 2.7 U/g) was obtained by A. sojae ATCC 20235 after 8 days at 30°C applying 30% sugar beet pulp as inducer substrate in combination with wheat bran as medium wetted at 160% with 0.2 M HCl. Furthermore, an overview of pectinolytic enzyme activities present in the extracts of both strains is provided. Protein profiles of both strains are given by SDS-PAGE electrophoresis, as well as zymograms for pectinolytic enzymes in comparison to commercial pectinase preparations.

摘要

以前鉴定出的酱油曲霉属真菌果胶酶产生菌被用于通过实验设计优化固态发酵中聚半乳糖醛酸酶的生产。在筛选和优化研究中,研究了培养基组成以及接种量、水分含量、培养时间和温度等几个工艺参数对聚半乳糖醛酸酶活性的影响。利用农业和农工业副产品建立了一种具有成本效益且可持续的酶生产工艺。在优化条件下比较酱油曲霉ATCC 20235和酱油曲霉CBS 100928的果胶酶生产情况,结果表明酱油曲霉ATCC 20235的聚半乳糖醛酸酶活性高6.9倍。酱油曲霉ATCC 20235在30℃下培养8天后,以30%的甜菜粕作为诱导底物,并与用0.2 M盐酸以160%湿度湿润的麦麸作为培养基,获得了最高酶产量(909.5±2.7 U/g)。此外,还提供了两种菌株提取物中存在的果胶分解酶活性的概述。通过SDS-PAGE电泳给出了两种菌株的蛋白质谱,以及与商业果胶酶制剂相比的果胶分解酶的酶谱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb27/4320240/fc5de266e0e1/40064_2014_Article_1501_Fig1_HTML.jpg

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