BACTERIAL AMYLASE PRODUCTION BY THE L-LACTIC ACID-PRODUCING STRAIN USING CASSAVA STARCH SUPPLEMENTED WITH RICE BRAN

Rattaporn Sumalu, C. Songsiriritthigul, J. Yongsawatdigul, S. Rodtong
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Abstract

Amylase is a crucial starch-degrading enzyme, which is commercially available, prvides benefit to starchy industry to overcome viscosity problem that caused by using high starch concentration, and to supply sugar residues. This study aimed to investigate the production of amylase by the potential optical pure L-lactic acid-producing Lactococcus sp. SUT 513 for further development of the optical pure acid fermentation process from the cheap cassava starch. Rice bran, the main byproduct in the process of rice milling, was found to provide the maximum amylase production when supplemented with 4.0 g/L (w/v) to the medium containing cassava starch (20.0 g/L, w/v), compared to the cassava medium added either the expensive nitrogen source, tryptone (5.0 g/L) and yeast extract (3.0 g/L, w/v); or the cheap alternatives, soy ptotein (8.0 g/L) or urea (2.0 g/L) combined with yeast extract (3.0 g/L). The amylase activity obtained from the developed medium was approximately 3 times higher than the original medium. This bacterium gave the highest crude amylase activity of 4.848±0.237 U/mL in the suitable medium performed in a7.5-L bioreactor with 3.0-L working volume for the optimal cultivation time of only 18 h under a control pH of 7.0, temperature at 35°C, agitation at 150 rpm, and without aeration. The results reveal the high potential production of amylase by Lactococcus sp. SUT 513 using the cheap cassava starch medium supplemented with rice bran, providing an opportunity to develop both amylase and optically pure L-lactic acid production processes.
利用木薯淀粉和米糠生产乳酸菌淀粉酶
淀粉酶是一种重要的淀粉降解酶,可通过商业途径获得,有利于淀粉工业克服因使用高浓度淀粉而产生的粘度问题,并提供糖渣。本研究旨在调查潜在的光纯 L-乳酸生产乳球菌 SUT 513 生产淀粉酶的情况,以便进一步开发利用廉价木薯淀粉的光纯酸发酵工艺。米糠是碾米过程中的主要副产品,在含有木薯淀粉(20.0 g/L,w/v)的木薯培养基相比,前者添加了昂贵的氮源--胰蛋白胨(5.0 g/L)和酵母提取物(3.0 g/L,w/v);后者添加了廉价的氮源--大豆蛋白胨(8.0 g/L)或尿素(2.0 g/L)和酵母提取物(3.0 g/L)。从开发的培养基中获得的淀粉酶活性大约是原始培养基的 3 倍。在控制 pH 值为 7.0、温度为 35°C、搅拌转速为 150 rpm、不通气的条件下,在工作容积为 3.0 L、培养时间为 18 h 的 7.5 L 生物反应器中,该细菌在合适的培养基中获得了最高的粗淀粉酶活性(4.848±0.237 U/mL)。结果表明,使用廉价的木薯淀粉培养基并辅以米糠,乳球菌 SUT 513 生产淀粉酶的潜力很大,这为开发淀粉酶和光学纯 L-乳酸生产工艺提供了机会。
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