植物乳杆菌发酵过程中生物碱对可可豆荚壳产乳酸影响的进一步研究

Dodi Irwanto, Wiratni Wiratni, R. Rochmadi, S. Syamsiah
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引用次数: 2

摘要

可可豆荚壳(CPH)是可可工业消化过程后产生的生物质废弃物。它约占可可新鲜果实的70-75%。CPH含有生物碱的活性化合物,被认为是使用微生物的乳酸发酵过程的抑制剂。本研究旨在通过进一步研究生物碱对植物乳杆菌发酵过程的影响,以CPH为原料生产乳酸。利用植物乳杆菌在50℃的条件下,在培养摇床中以100 rpm搅拌48 h。通过对比底物(葡萄糖)的消耗、细胞的干重和乳酸的产生来分析添加生物碱的效果。根据为研究案例准备的动力学模型的参数值,对不同处理下微生物性能的差异进行了评估。动力学模型拟合结果表明,生物碱的存在使产物的生长模式从生长相关产物转变为混合生长模式,因为产物是在缓慢生长和固定阶段形成的。不同添加量下的最大生长速率(μm)和底物抑制常数(Ks)可能保持不变,分别为0.69 h-1和3.89 g/L,因为这些参数不受添加量的影响
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lactic Acid Production From Cocoa Pod Husk by Studying Further the Influence of Alkaloids on Fermentation Process using Lactobacillus Plantarum Bacteria
Cocoa Pod Husk (CPH) is the biomass waste from cocoa industry, generated after the digestion process. It accounts for about 70-75% of the cocoa fresh fruit. CPH contains active compounds of alkaloids that are thought to be the inhibitors of the lactic acid fermentation process using microorganisms. This study aims to produce Lactic Acid from CPH by studying further the influence of alkaloids on fermentation process using Lactobacillus plantarum bacteria. Fermentation using Lactobacillus plantarum bacteria was carried out at 50°C and with agitation at 100 rpm in incubator shaker for 48 h. This process was conducted to determine the effect of the addition of alkaloids by analyzing through the comparison between the consumption of substrate (glucose), dry weight of the cell, and the production of lactic acid. Evaluation of the differences in the performance of microorganisms at various treatments was performed based on the parameters values of the kinetic models prepared for the case studied. The kinetic model fitting results showed that the presence of alkaloids alters the growth patterns of products from growth-associated products into mixed patterns because the products were formed during slow growth and stationary phases. The maximum growth rate (μm) and substrate inhibition constant (Ks) obtained on each variation of inhibitor addition were likely to remain constant at the values of 0.69 h-1 and 3.89 g/L respectively, as these parameters were unaffected by the addition of inhibitor
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