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通过随机诱变和优化发酵条件提高野生型蛋白含量。

Enhancing Protein Content in Wild-Type via Random Mutagenesis and Optimized Fermentation Conditions.

机构信息

Department of Food Science and Biotechnology, Chung-Ang University, Anseong 17546, Republic of Korea.

GreenTech-based Food Safety Research Group, BK21 Four, Chung-Ang University, Anseong 17546, Republic of Korea.

出版信息

J Microbiol Biotechnol. 2024 Sep 28;34(9):1912-1918. doi: 10.4014/jmb.2405.05027. Epub 2024 Jul 31.

Abstract

Single-cell protein (SCP) derived from microorganisms is widely recognized as a viable alternative protein source for the future. Nevertheless, the commercialization of yeast-based SCP is hampered by its relatively low protein content. Therefore, this study aimed to enhance the protein content of via random mutagenesis. To achieve this, KCCM 51811, which exhibited the highest protein concentration among 20 edible strains, was selected as a chassis strain. Subsequently, a KCCM 51811 mutant library was constructed (through UV irradiation) and screened to isolate mutants exhibiting high protein content and/or concentration. Among the 174 mutant strains studied, the #126 mutant exhibited a remarkable 43% and 36% higher protein content and concentration, respectively, compared to the parental strain. Finally, the #126 mutant was cultured in a fed-batch system using molasses and corn-steep liquor, resulting in a protein concentration of 21.6 g/l in 100 h, which was 18% higher than that produced by the parental strain. These findings underscore the potential of our approach for the cost-effective production of food-grade SCP.

摘要

单细胞蛋白(SCP)来源于微生物,被广泛认为是未来可行的替代蛋白质来源。然而,基于酵母的 SCP 的商业化受到其相对较低的蛋白质含量的阻碍。因此,本研究旨在通过随机诱变来提高 的蛋白质含量。为了实现这一目标,选择了 KCCM 51811 作为底盘菌株,该菌株在 20 种可食用 菌株中表现出最高的蛋白质浓度。随后,构建了 KCCM 51811 突变体文库(通过紫外线照射)并进行筛选,以分离出具有高蛋白含量和/或浓度的突变体。在研究的 174 株突变株中,#126 突变株的蛋白质含量和浓度分别比亲本菌株高出 43%和 36%。最后,#126 突变株在分批补料系统中使用糖蜜和玉米浆进行培养,在 100 小时内产生了 21.6 g/l 的蛋白质浓度,比亲本菌株高出 18%。这些发现强调了我们的方法在经济高效地生产食品级 SCP 方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af4d/11485558/f0e09a13e077/jmb-34-9-1912-f1.jpg

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