利用从木薯加工厂酵母菌株中分离出的外源粗淀粉酶和纤维素酶组合,优化高粱提取物的回收率

O.P. Nnaemeka , C.A. Nwachukwu , I.A. Ndubuisi , A.N. Moneke , R.C. Agu , B.N. Okolo , O.C. Amadi
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引用次数: 0

摘要

从木薯加工厂分离出来的酵母菌的粗酶提取物被用于优化高粱或发芽高粱的提取物回收。众所周知,微生物酶在工业流程中非常有益,因为它们具有各种优势。微生物的繁殖速度非常快,并在加工过程中产生多种酶。在许多自然环境中,这种具有生产工业粗酶潜力的微生物比比皆是。本研究考察了从木薯磨坊中分离出来的酵母菌株(SP40 和 SS12)的粗酶提取物(戊聚糖酶和淀粉酶)的性能。在谷物高粱和发芽高粱的糖化过程中,使用不同的酶组合提取粗酶,研究它们对麦汁比重(SG)、还原糖(RS)和游离氨基酸氮(FAN)质量的影响。倾析糖化过程保护了酶和胶化的高粱淀粉,对生产较高 SG、RS 和 FAN 产品的麦汁更为有效。对照酶(低剂量)产生的麦汁 SG 分别为 1.034(灌注糖化)和 1.056(倾析糖化)。试验酶(较低剂量)的麦汁 SG 值也很高,分别为 1.018(输液糖化)和 1.034(倾析糖化)。SP40 和 SS12 中的纤维素酶和淀粉酶活性相似,因为这两种微生物主要产生淀粉水解酶。从这项研究来看,粗酶与商业酶相比,使用较低剂量的粗酶提取物就能生产出较高 SG、RS 和 FAN 产品的麦汁,这将为工业节省成本。糖化制度也是一个需要考虑的重要因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optimizing extract recovery from sorghum using combinations of exogenous crude amylase and pullulanase isolated from yeast strains from cassava mill factory

Crude enzyme extracts of yeasts isolated from a cassava mill factory were utilized in optimizing extract recovery from sorghum or malted sorghum. Microbial enzymes are known to be very beneficial in industrial processes due to various advantages derived from them. Micro-organisms multiply very rapidly and produce diverse enzymes during the process. Such micro-organisms with potential to produce industrial crude enzymes abound in many natural environments. This study examined the performance of crude enzyme extracts (pullulanase and amylase) from yeasts strains (SP40 and SS12) isolated from a cassava mill factory. The crude enzyme extracts were used in mashing grain sorghum and malted sorghum using various enzyme combinations to study their effects on quality of wort specific gravity (SG), reducing sugars (RS) and free amino nitrogen (FAN). The decantation mashing process which protected the enzymes and gelatinized sorghum starch was more effective in producing wort of higher SG, RS and FAN products. Control enzyme (lower doses) gave wort SG of 1.034 (infusion mashing) and 1.056 (decantation mashing). Test enzymes (lower doses) also gave good wort SG of 1.018 (infusion mashing) and 1.034 (decantation mashing). The activities of pullulanase and amylase from SP40 and SS12 were similar because both microorganisms produced mainly starch hydrolysing enzymes. From this study, the crude enzymes compared well with commercial enzymes in using lower doses of the crude enzyme extract to produce wort of higher SG, RS and FAN products and this will save costs for the industry. The mashing regime is also an important factor to consider.

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