Ashok Anup, Devarai Santhosh Kumar
Industrial Bioprocess and Bioprospecting Laboratory (IBBL), Department of Chemical Engineering, Indian Institute of Technology Hyderabad, Kandi, Sangareddy, Telangana 502285 India.
3 Biotech. 2019 Sep;9(9):349. doi: 10.1007/s13205-019-1883-5. Epub 2019 Aug 31.
The present work reports on the production of extracellular l-asparaginase from IBBL-2 using submerged fermentation (SmF) process free of glutaminase and urease activities. Primary studies done in shake flask showed that the highest l-asparaginase activity of 12.68 U mL was produced at 72 h with optimized fermentation parameters such as pH 6.0, 4 × 10 fungal cells mL, and agitation of 180 rpm at 30 °C using one-factor-at-a-time (OFAT). Different substrates, nitrogen sources, temperature, pH, the initial number of cells and metal ions were tested to determine the impact on enzyme production. l-Asparaginase activity of 17.68 U mL was produced after 48 h using immobilized calcium-alginate (Ca-alginate) cells. 4 × 10 cells mL was entrapped in 3% (W/V) of alginate bead of size 2 mm each at a temperature of 30 °C and pH of 6. The process was optimized using L9 (3) Taguchi Orthogonal Array (OA) technique with a regression coefficient ( ) value of 0.9709, value of 33.34 and value of 0.0025. Scale-up studies involving 200-mL and 1-L rotating bed reactor (RBR) using immobilized beads were done and the results obtained are 20.21 U mL and 19.13 U mL, respectively, the increased activity with immobilization accounts for reduced shear on cells due to increased stability as compared to the free-flowing cells.
本研究报道了利用深层发酵(SmF)工艺从IBBL-2生产无谷氨酰胺酶和脲酶活性的细胞外L-天冬酰胺酶。摇瓶中的初步研究表明,在优化的发酵参数(如pH 6.0、4×10个真菌细胞/mL、30℃下180 rpm的搅拌速度)下,采用一次单因素(OFAT)法,在72 h时产生的最高L-天冬酰胺酶活性为12.68 U/mL。测试了不同的底物、氮源、温度、pH、细胞初始数量和金属离子,以确定对酶生产的影响。使用固定化海藻酸钙(Ca-藻酸盐)细胞在48 h后产生了17.68 U/mL的L-天冬酰胺酶活性。在30℃和pH 6的条件下,将4×10个细胞/mL包埋在3%(W/V)的2 mm大小的藻酸盐珠中。使用L9(3)田口正交阵列(OA)技术对该工艺进行了优化,回归系数()值为0.9709,值为33.34,值为0.0025。进行了涉及200 mL和1 L旋转床反应器(RBR)的放大研究,使用固定化珠子,得到的结果分别为20.21 U/mL和19.13 U/mL,与自由流动的细胞相比,固定化导致的活性增加是由于细胞稳定性增加,剪切力降低。