Utilization of non-concentrated banana pseudostem sap waste for converting to bioethanol: In vitro and in silico evidence

Praveen Kumar Gupta , Soumya Basu , Vikas Rana , Shuank Malik , Amritendu Panchadhyayee
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Abstract

The abundantly available waste banana pseudostem fibers have attracted the paper and textile industries, however the stem-sap extracted during fiber processing remains underutilized. Although this sap comprising cellulosic sugars holds potential as a feedstock, its commercial viability in the renewable energy sector remains a challenge. Our study delves into this untapped resource by mechanically extracting sap from banana pseudostems and enhancing its reducing sugar content to approximately 35.5 g/L through acid hydrolysis and detoxification without concentrating the sap. Using separate batch fermentations with pentose and hexose fermenting strains such as Pichia stipitis NCIM 3499 and Saccharomyces cerevisiae ATCC 2601, we achieved bioethanol production efficiencies of 67.5 % and 70.03 %, respectively. Yield and cost analyses confirmed the feasibility of this approach for industrial application in low-economy settings. Furthermore, gene-interaction network and functional enrichment analysis identified 63 key genes involved in carbohydrate metabolism and ethanol conversion pathways within the fermenting organisms. Among these, the PGK1 gene and its direct interactors emerged as promising targets for future biotechnological enhancements aimed at boosting bioethanol production. This study not only underscores the renewable energy potential of unconcentrated banana pseudostem sap but also paves the way for innovative genetic interventions to optimize bioethanol yields.

利用非浓缩香蕉假茎汁液废料转化为生物乙醇:体外和硅学证据
大量的香蕉假茎废纤维吸引了造纸和纺织行业,但在纤维加工过程中提取的茎汁仍未得到充分利用。虽然这种含有纤维素糖的汁液具有作为原料的潜力,但其在可再生能源领域的商业可行性仍是一个挑战。我们的研究通过机械方法从香蕉假茎中提取汁液,并在不浓缩汁液的情况下通过酸水解和解毒将还原糖含量提高到约 35.5 克/升,从而深入研究了这一尚未开发的资源。通过使用戊糖和己糖发酵菌株(如 Pichia stipitis NCIM 3499 和 Saccharomyces cerevisiae ATCC 2601)进行独立批量发酵,我们的生物乙醇生产效率分别达到了 67.5 % 和 70.03 %。产量和成本分析证实了这种方法在低经济环境下工业应用的可行性。此外,基因相互作用网络和功能富集分析确定了发酵生物体内参与碳水化合物代谢和乙醇转化途径的 63 个关键基因。在这些基因中,PGK1 基因及其直接相互作用因子成为未来生物技术改进的有望目标,旨在提高生物乙醇产量。这项研究不仅强调了未浓缩香蕉假茎汁液的可再生能源潜力,还为优化生物乙醇产量的创新基因干预铺平了道路。
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