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原位萃取发酵增加细胞膜通透性,提高樟芝 S-29 中antroquinonol 的产量。

An increase in cell membrane permeability in the in situ extractive fermentation improves the production of antroquinonol from Antrodia camphorata S-29.

机构信息

Shanghai Engineering Research Center of Food Microbiology, School of Medical Instrument and Food Engineering, University of Shanghai for Science and Technology, Shanghai, 200093, People's Republic of China.

Institute of Bast Fiber Crops, Chinese Academy of Agricultural Sciences, Changsha, 410205, People's Republic of China.

出版信息

J Ind Microbiol Biotechnol. 2020 Feb;47(2):197-207. doi: 10.1007/s10295-020-02258-8. Epub 2020 Jan 14.

Abstract

The goals of this study were to increase the production of antroquinonol (AQ) and to elucidate the response mechanism of the cell membrane during the in situ extractive fermentation (ISEF) of Antrodia camphorata S-29. Through ISEF, the concentration of AQ reached a maximum of 146.1 ± 2.8 mg/L, which was approximately (7.4 ± 0.1)-fold that of the control (coenzyme Q-induced fermentation). Transcriptome sequencing showed that four genes (FAD2, fabG, SCD, and FAS1) related to fatty acid biosynthesis were upregulated. FAD2 and SCD may regulate the increase in oleic acid (C18:1) and linoleic acid (C18:2) in the cell membrane of A. camphorata S-29, resulting in an increase in cell membrane permeability. AQ was successfully transferred to the n-tetradecane phase through the cell membrane, reducing product feedback inhibition and improving the production of AQ from A. camphorata S-29.

摘要

本研究旨在提高樟芝(Antrodia camphorata S-29)中antroquinonol(AQ)的产量,并阐明细胞膜在原位萃取发酵(ISEF)过程中的响应机制。通过 ISEF,AQ 的浓度最高达到 146.1 ± 2.8 mg/L,约为对照(辅酶 Q 诱导发酵)的 7.4 ± 0.1 倍。转录组测序表明,与脂肪酸生物合成相关的四个基因(FAD2、fabG、SCD 和 FAS1)上调。FAD2 和 SCD 可能调节樟芝细胞膜中油酸(C18:1)和亚油酸(C18:2)的增加,导致细胞膜通透性增加。AQ 通过细胞膜成功转移到正十四烷相中,减少了产物反馈抑制,提高了樟芝 S-29 中 AQ 的产量。

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