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利用玉米芯作为木聚糖分解酵母菌株的固定化基质

Utilization of Corncob as an Immobilization Matrix for a Xylanolytic Yeast Strain.

作者信息

Aftab Maham, Ejaz Uroosa, Pashameah Rami Adel, Fatima Aimen, Syed Jaweria, Ansari Immad, Sohail Muhammad, AlSubhi Samah A, Alzahrani Eman, El-Bahy Zeinhom M

机构信息

Department of Biosciences, Faculty of Life Sciences, Shaheed Zulfikar Ali Bhutto Institute of Science and Technology (SZABIST), Karachi 75600, Pakistan.

Department of Chemistry, Faculty of Applied Science, Umm Al-Qura University, Makkah 24230, Saudi Arabia.

出版信息

Polymers (Basel). 2023 Jan 29;15(3):683. doi: 10.3390/polym15030683.

Abstract

Immobilization of microbial cells for the production of industrially important enzymes has been reported to offer the advantages of recyclability, higher yields and cost effectiveness. The search for an appropriate matrix that is affordable and easy to prepare is a significant topic in microbial biotechnology. Here, an abundant type of agro-industrial waste-corncob-was utilized as an immobilization matrix for the production of xylanase from an indigenous yeast strain, MK-157. This is the first report describing xylanase production from immobilized . To render the corncob matrix more porous, alkaline pretreatment was undertaken and yeast cells were immobilized on the matrix by cultivating at 30 °C for 48 h in Sabouraud dextrose broth. After incubation, the immobilized matrix was transferred to mineral salt medium containing 1% xylan and incubated at 30 °C for 24 h. Xylanase production was determined in cell-free culture supernatant and the matrix was recycled for up to seven cycles. Moreover, xylanase-mediated saccharification was carried out using sugarcane bagasse as a substrate and the release of reducing sugars was monitored. The results showed that the immobilized yeast produced 4.97 IU mL xylanase in the first production cycle, indicating a >tenfold increase compared to the free cells. Xylanase production further increased to its maximum levels (9.23 IU mL) in the fourth production cycle. Nonetheless, the cells retained 100% productivity for up to seven cycles. The volumetric and specific productivity of xylanase were also the highest in the fourth cycle. Scanning electron microscopy images revealed the rough surface of the untreated corncob, which became more porous after alkaline pretreatment. Immobilized yeast cells were also visible on the corncob pieces. The saccharification of a natural resource-sugarcane bagasse-using xylanase preparation yielded 26 mg L of reducing sugars. Therefore, it can be concluded that yeast strains can yield sufficient quantities of xylanase, allowing possible biotechnological applications. Moreover, corncob can serve as a cost-effective matrix for industrially important yeast strains.

摘要

据报道,固定化微生物细胞用于生产具有重要工业价值的酶具有可回收、产量高和成本效益高的优点。寻找一种价格合理且易于制备的合适基质是微生物生物技术中的一个重要课题。在此,一种丰富的农业工业废料——玉米芯——被用作固定化基质,用于从本地酵母菌株MK - 157生产木聚糖酶。这是第一份描述固定化细胞生产木聚糖酶的报告。为了使玉米芯基质更具多孔性,进行了碱性预处理,并通过在沙氏葡萄糖肉汤中于30°C培养48小时将酵母细胞固定在基质上。培养后,将固定化基质转移到含有1%木聚糖的矿物盐培养基中,并于30°C培养24小时。在无细胞培养上清液中测定木聚糖酶的产量,并将基质循环使用多达七个周期。此外,以甘蔗渣为底物进行木聚糖酶介导的糖化反应,并监测还原糖的释放。结果表明,固定化酵母在第一个生产周期产生4.97 IU/mL木聚糖酶,与游离细胞相比增加了十倍以上。木聚糖酶产量在第四个生产周期进一步增加到最高水平(9.23 IU/mL)。尽管如此,细胞在多达七个周期内保持100%的生产力。木聚糖酶的体积生产力和比生产力在第四个周期也最高。扫描电子显微镜图像显示未处理玉米芯的表面粗糙,碱性预处理后变得更具多孔性。在玉米芯碎片上也可见固定化的酵母细胞。使用木聚糖酶制剂对自然资源甘蔗渣进行糖化反应产生了26 mg/L的还原糖。因此,可以得出结论,酵母菌株可以产生足够数量的木聚糖酶,从而实现可能的生物技术应用。此外,玉米芯可以作为具有重要工业价值的酵母菌株的经济有效的基质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4996/9920909/5b10787d262a/polymers-15-00683-g001.jpg

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