{"title":"冬虫夏草通过法定人数感应系统提高多糖产量","authors":"Huang Qiao, Jianshu Chen, Shengli Yang","doi":"10.1002/jobm.202400103","DOIUrl":null,"url":null,"abstract":"<p>This study aimed to enhance extracellular polysaccharide (EPS) production in <i>Cordyceps militaris</i> by constructing a quorum sensing (QS) system to regulate the expression of biosynthetic enzyme genes, including <i>phosphoglucomutase</i>, <i>hexokinase</i>, <i>phosphomannomutase</i>, <i>polysaccharide synthase</i>, and <i>UDP-glucose 4-epimerase</i> genes. The study found higher EPS concentrations in seven recombinant strains compared to the wild-type <i>C. militaris</i>, indicating that the overexpression of key enzyme genes increased EPS production. Among them, the CM-<i>pgm</i>-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 <i>C. militaris</i> strain. Additionally, the regulatory effects of aromatic amino acids on the QS system of the CM-<i>pgm</i>-2 strain were investigated. Under the influence of 45 mg/L tryptophan, the EPS production in CM-<i>pgm</i>-2 reached 4.75 ± 0.20 g/L, representing a 1.90-fold increase compared to wild <i>C. militaris</i> strains. This study provided an effective method for the large-scale production of EPSs in <i>C. militaris</i>, and opened up new avenues for research into fungal QS mechanisms.</p>","PeriodicalId":15101,"journal":{"name":"Journal of Basic Microbiology","volume":"64 7","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2024-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Enhanced polysaccharide production through quorum sensing system in Cordyceps militaris\",\"authors\":\"Huang Qiao, Jianshu Chen, Shengli Yang\",\"doi\":\"10.1002/jobm.202400103\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>This study aimed to enhance extracellular polysaccharide (EPS) production in <i>Cordyceps militaris</i> by constructing a quorum sensing (QS) system to regulate the expression of biosynthetic enzyme genes, including <i>phosphoglucomutase</i>, <i>hexokinase</i>, <i>phosphomannomutase</i>, <i>polysaccharide synthase</i>, and <i>UDP-glucose 4-epimerase</i> genes. The study found higher EPS concentrations in seven recombinant strains compared to the wild-type <i>C. militaris</i>, indicating that the overexpression of key enzyme genes increased EPS production. Among them, the CM-<i>pgm</i>-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 <i>C. militaris</i> strain. Additionally, the regulatory effects of aromatic amino acids on the QS system of the CM-<i>pgm</i>-2 strain were investigated. Under the influence of 45 mg/L tryptophan, the EPS production in CM-<i>pgm</i>-2 reached 4.75 ± 0.20 g/L, representing a 1.90-fold increase compared to wild <i>C. militaris</i> strains. This study provided an effective method for the large-scale production of EPSs in <i>C. militaris</i>, and opened up new avenues for research into fungal QS mechanisms.</p>\",\"PeriodicalId\":15101,\"journal\":{\"name\":\"Journal of Basic Microbiology\",\"volume\":\"64 7\",\"pages\":\"\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2024-05-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Basic Microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/jobm.202400103\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Basic Microbiology","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jobm.202400103","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Enhanced polysaccharide production through quorum sensing system in Cordyceps militaris
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.
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).