Enhanced polysaccharide production through quorum sensing system in Cordyceps militaris

IF 3.5 4区 生物学 Q2 MICROBIOLOGY Journal of Basic Microbiology Pub Date : 2024-05-21 DOI:10.1002/jobm.202400103
Huang Qiao, Jianshu Chen, Shengli Yang
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Abstract

This study aimed to enhance extracellular polysaccharide (EPS) production in Cordyceps militaris by constructing a quorum sensing (QS) system to regulate the expression of biosynthetic enzyme genes, including phosphoglucomutase, hexokinase, phosphomannomutase, polysaccharide synthase, and UDP-glucose 4-epimerase genes. The study found higher EPS concentrations in seven recombinant strains compared to the wild-type C. militaris, indicating that the overexpression of key enzyme genes increased EPS production. Among them, the CM-pgm-2 strain exhibited the highest EPS production, reaching a concentration of 3.82 ± 0.26 g/L, which was 1.52 times higher than the amount produced by the wild C. militaris strain. Additionally, the regulatory effects of aromatic amino acids on the QS system of the CM-pgm-2 strain were investigated. Under the influence of 45 mg/L tryptophan, the EPS production in CM-pgm-2 reached 4.75 ± 0.20 g/L, representing a 1.90-fold increase compared to wild C. militaris strains. This study provided an effective method for the large-scale production of EPSs in C. militaris, and opened up new avenues for research into fungal QS mechanisms.

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冬虫夏草通过法定人数感应系统提高多糖产量
本研究旨在通过构建一个法定量感应(QS)系统来调控冬虫夏草生物合成酶基因的表达,包括磷酸葡萄糖转氨酶、己糖激酶、磷酸甘露转氨酶、多糖合成酶和 UDP-葡萄糖 4-表聚酶基因,从而提高冬虫夏草细胞外多糖(EPS)的产量。研究发现,与野生型米氏杆菌相比,7 个重组菌株的 EPS 浓度更高,这表明关键酶基因的过度表达增加了 EPS 的产量。其中,CM-pgm-2 菌株的 EPS 产量最高,达到 3.82 ± 0.26 克/升,是野生型 C. militaris 菌株产量的 1.52 倍。此外,还研究了芳香族氨基酸对 CM-pgm-2 菌株 QS 系统的调节作用。在 45 mg/L 色氨酸的影响下,CM-pgm-2 的 EPS 产量达到 4.75 ± 0.20 g/L,是野生 C. militaris 菌株产量的 1.90 倍。该研究为军事菌大规模生产 EPS 提供了有效方法,为真菌 QS 机制的研究开辟了新途径。
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来源期刊
Journal of Basic Microbiology
Journal of Basic Microbiology 生物-微生物学
CiteScore
6.10
自引率
0.00%
发文量
134
审稿时长
1.8 months
期刊介绍: The Journal of Basic Microbiology (JBM) publishes primary research papers on both procaryotic and eucaryotic microorganisms, including bacteria, archaea, fungi, algae, protozoans, phages, viruses, viroids and prions. Papers published deal with: microbial interactions (pathogenic, mutualistic, environmental), ecology, physiology, genetics and cell biology/development, new methodologies, i.e., new imaging technologies (e.g. video-fluorescence microscopy, modern TEM applications) novel molecular biology methods (e.g. PCR-based gene targeting or cassettes for cloning of GFP constructs).
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