Pervez Sidra, Aman Afsheen, Iqbal Samina, Siddiqui Nadir Naveed, Ul Qader Shah Ali
The Karachi Institute of Biotechnology & Genetic Engineering (KIBGE), University of Karachi, Karachi -75270, Pakistan.
BMC Biotechnol. 2014 May 29;14:49. doi: 10.1186/1472-6750-14-49.
Cassava starch is considered as a potential source for the commercial production of bioethanol because of its availability and low market price. It can be used as a basic source to support large-scale biological production of bioethanol using microbial amylases. With the progression and advancement in enzymology, starch liquefying and saccharifying enzymes are preferred for the conversion of complex starch polymer into various valuable metabolites. These hydrolytic enzymes can selectively cleave the internal linkages of starch molecule to produce free glucose which can be utilized to produce bioethanol by microbial fermentation.
In the present study, several filamentous fungi were screened for production of amylases and among them Aspergillus fumigatus KIBGE-IB33 was selected based on maximum enzyme yield. Maximum α-amylase, amyloglucosidase and glucose formation was achieved after 03 days of fermentation using cassava starch. After salt precipitation, fold purification of α-amylase and amyloglucosidase increased up to 4.1 and 4.2 times with specific activity of 9.2 kUmg⁻¹ and 393 kUmg⁻¹, respectively. Concentrated amylolytic enzyme mixture was incorporated in cassava starch slurry to give maximum glucose formation (40.0 gL⁻¹), which was further fermented using Saccharomyces cerevisiae into bioethanol with 84.0% yield. The distillate originated after recovery of bioethanol gave 53.0% yield.
An improved and effective dual enzymatic starch degradation method is designed for the production of bioethanol using cassava starch. The technique developed is more profitable due to its fast liquefaction and saccharification approach that was employed for the formation of glucose and ultimately resulted in higher yields of alcohol production.
木薯淀粉因其可得性和低市场价格,被视为生物乙醇商业化生产的潜在原料。它可作为利用微生物淀粉酶大规模生物生产生物乙醇的基础原料。随着酶学的发展与进步,淀粉液化酶和糖化酶更适合将复杂的淀粉聚合物转化为各种有价值的代谢产物。这些水解酶能选择性地切断淀粉分子的内部连接键,产生游离葡萄糖,进而通过微生物发酵用于生产生物乙醇。
在本研究中,筛选了几种丝状真菌用于淀粉酶的生产,其中烟曲霉KIBGE - IB33基于最高酶产量被选中。使用木薯淀粉发酵03天后,α -淀粉酶、糖化酶和葡萄糖的产量达到最高。盐析后,α -淀粉酶和糖化酶的纯化倍数分别提高到4.1倍和4.2倍,比活性分别为9.2 kUmg⁻¹和393 kUmg⁻¹。将浓缩的淀粉酶混合物加入木薯淀粉浆中,可产生最大葡萄糖产量(40.0 gL⁻¹),进一步用酿酒酵母发酵成生物乙醇,产率为84.0%。生物乙醇回收后得到的馏出物产率为53.0%。
设计了一种改进且有效的双酶淀粉降解方法,用于以木薯淀粉生产生物乙醇。所开发的技术因其快速液化和糖化方法而更具盈利性,该方法用于形成葡萄糖,最终导致更高的酒精产量。