Yadav Sangeeta, Yadav Pramod Kumar, Yadav Dinesh, Yadav Kapil Deo Singh
Department of Chemistry, Deen Dayal Upadhyaya Gorakhpur University, Uttar Pradesh, India.
Appl Biochem Biotechnol. 2009 Oct;159(1):270-83. doi: 10.1007/s12010-008-8471-1. Epub 2008 Dec 17.
An indigenously isolated fungal strain identified as Aspergillus terricola with assigned fungal strain number MTCC 7588 has been used as source for pectin lyase production. The extracellular pectin lyase was purified to homogeneity from the culture filtrate of A. terricola by ion exchange and gel filtration chromatography. The determined molecular weight was 35 +/- 01 kDa. The K(m) and k(cat) (turnover) values of the purified enzyme at 37 degrees C using citrus pectin as the substrate were found to be 1.0 mg/ml and 110.0 s(-1), respectively. The pH and temperature optima of the enzyme were 8.0 and 50 degrees C, respectively. The retting ability of the purified pectin lyase for natural fibers viz. Cannabis sativa and Linum usitatissimum has been demonstrated for the first time.
一种本土分离的真菌菌株,被鉴定为土曲霉,菌株编号为MTCC 7588,已被用作生产果胶裂解酶的来源。通过离子交换和凝胶过滤色谱法从土曲霉的培养滤液中纯化细胞外果胶裂解酶至均一性。测定的分子量为35±01 kDa。以柑橘果胶为底物,在37℃下纯化酶的K(m)和k(cat)(周转)值分别为1.0 mg/ml和110.0 s(-1)。该酶的最适pH和温度分别为8.0和50℃。首次证明了纯化的果胶裂解酶对天然纤维(即大麻和亚麻)的脱胶能力。