Sinha Sujata, Chand Subhash, Tripathi Pushplata
Department of Biochemical Engineering and Biotechnology, Indian Institute of Technology, Delhi, 110016, India.
School of Sciences, Indira Gandhi National Open University, Maidan Garhi, New Delhi, 68, India.
3 Biotech. 2016 Jun;6(1):13. doi: 10.1007/s13205-015-0330-5. Epub 2016 Jan 6.
Exochitosanase secreting fungus (A. fumigatus IIT-004) was isolated from fish waste using 1 % (w/v) chitosan as sole carbon source after multistage screening. Chitosan-dependent exochitosanase enzyme production (6 IU ml) in log phase of growth (chitosan utilization rate 0.11 g g cell h) was observed for Aspergillus fumigatus in chitosan minimal salt medium and there was no enzyme production in glucose medium. Enzyme production was found to be extracellular and subjected to purification by a number of steps like acetone fractionation as well as column chromatography. 40 % yield and 26-fold of enzyme purification was achieved after all the steps. Purified enzyme was characterized for optimum temperature, pH, ionic strength and substrate specificity. The K and V for purified exochitosanase enzyme was calculated to be 8 mg ml and 5.2 × 10 mol mg min. Enzyme was immobilized on polyacrylonitrile nanofibres membrane matrix by adsorption as well as amidination. Enzymatic production of glucosamine was achieved using various chitosan substrates by free/immobilized exochitosanase and compared. Isolated and purified exochitosanase also showed transglycosylation activity.
通过多阶段筛选,以1%(w/v)壳聚糖作为唯一碳源,从鱼废料中分离出了分泌外切壳聚糖酶的真菌(烟曲霉IIT-004)。在壳聚糖基本盐培养基中,观察到烟曲霉在生长对数期产生依赖壳聚糖的外切壳聚糖酶(6 IU/ml)(壳聚糖利用率为0.11 g/g细胞·h),而在葡萄糖培养基中不产生酶。发现酶的产生是细胞外的,并通过丙酮分级分离以及柱色谱等多个步骤进行纯化。经过所有步骤后,获得了40%的产率和26倍的酶纯化倍数。对纯化后的酶进行了最佳温度、pH、离子强度和底物特异性的表征。纯化后的外切壳聚糖酶的Km和Vmax经计算分别为8 mg/ml和5.2×10⁻⁵ mol·mg⁻¹·min⁻¹。通过吸附以及酰胺化作用将酶固定在聚丙烯腈纳米纤维膜基质上。使用各种壳聚糖底物,通过游离/固定化外切壳聚糖酶实现了氨基葡萄糖的酶促生产,并进行了比较。分离和纯化的外切壳聚糖酶还表现出转糖基化活性。