从橘子皮分解中分离的根霉聚半乳糖醛酸酶的生产、纯化和特性研究。

Q2 Biochemistry, Genetics and Molecular Biology
Enzyme Research Pub Date : 2012-01-01 Epub Date: 2012-10-17 DOI:10.1155/2012/138634
Mohd Asif Siddiqui, Veena Pande, Mohammad Arif
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引用次数: 42

摘要

通过对40株不同菌株的初步筛选,分离出一株产聚半乳糖醛酸酶的嗜热真菌。该真菌经印度昌迪加尔微生物类型培养集(MTCC)鉴定为pusilis根霉。采用Sephadex G-200和sepphacryl S-100两步色谱法纯化了一种胞外聚半乳糖醛酸酶(PGase)。纯化后的酶为单体,分子量为32 kDa。PGase在55℃、pH 5.0条件下活性最佳。在50°C、120 min的孵育条件下稳定,pH值在4.0 ~ 5.0之间。PGase的稳定性在60℃以上和pH 5.0以上迅速下降。表观K(m)和V(max)分别为0.22 mg/mL和4.34 U/mL。这是首次从该物种中分离到聚半乳糖醛酸酶。利用该菌株生产聚半乳糖醛酸酶是有价值的。该菌株的聚半乳糖醛酸酶可推荐用于商业生产,因为它的组成和较少的分解代谢抑制性质,热稳定性,广泛的pH范围和较低的K(m)性质。但是,为了更好地用于商业生产,需要进行规模研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Production, Purification, and Characterization of Polygalacturonase from Rhizomucor pusillus Isolated from Decomposting Orange Peels.

Production, Purification, and Characterization of Polygalacturonase from Rhizomucor pusillus Isolated from Decomposting Orange Peels.

Production, Purification, and Characterization of Polygalacturonase from Rhizomucor pusillus Isolated from Decomposting Orange Peels.

Production, Purification, and Characterization of Polygalacturonase from Rhizomucor pusillus Isolated from Decomposting Orange Peels.

A thermophilic fungal strain producing polygalacturonase was isolated after primary screening of 40 different isolates. The fungus was identified as Rhizomucor pusilis by Microbial Type Culture Collection (MTCC), Chandigarh, India. An extracellular polygalacturonase (PGase) from R. pusilis was purified to homogeneity by two chromatographic steps using Sephadex G-200 and Sephacryl S-100. The purified enzyme was a monomer with a molecular weight of 32 kDa. The PGase was optimally active at 55°C and at pH 5.0. It was stable up to 50°C for 120 min of incubation and pH condition between 4.0 and 5.0. The stability of PGase decreases rapidly above 60°C and above pH 5.0. The apparent K(m) and V(max) values were 0.22 mg/mL and 4.34 U/mL, respectively. It was the first time that a polygalacturonase enzyme was purified in this species. It would be worthwhile to exploit this strain for polygalacturonase production. Polygalacturonase from this strain can be recommended for the commercial production because of its constitutive and less catabolically repressive nature, thermostability, wide range of pH, and lower K(m) properties. However, scale-up studies are needed for the better output for commercial production.

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来源期刊
Enzyme Research
Enzyme Research Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
4.60
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