Xiaona Chen, Ning Zhu, Guangrui Yang, Xiaopeng Guo, Shangchen Sun, Feifan Leng, Yonggang Wang
{"title":"cspA 对用氯化钙法制备大肠杆菌合格细胞的作用","authors":"Xiaona Chen, Ning Zhu, Guangrui Yang, Xiaopeng Guo, Shangchen Sun, Feifan Leng, Yonggang Wang","doi":"10.1002/jobm.202400113","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>One of the fundamental techniques in genetic engineering is the creation of <i>Escherichia coli</i> competent cells using the CaCl<sub>2</sub> method. However, little is known about the mechanism of <i>E. coli</i> competence formation. We have previously found that the <i>cspA</i> gene may play an indispensable role in the preparation of <i>E. coli</i> DH5α competent cells through multiomics analysis. In the present study, the cellular localization, physicochemical properties, and function of the protein expressed by the <i>cspA</i> gene were analyzed. To investigate the role of the <i>cspA</i> gene in <i>E. coli</i> transformation, <i>cspA-</i>deficient mutant was constructed by red homologous recombination. The growth, transformation efficiency, and cell morphology of the <i>cspA-</i>deficient strain and <i>E. coli</i> were compared. It was found that there were no noticeable differences in growth and morphology between <i>E. coli</i> and the <i>cspA-</i>deficient strain cultured at 37°C, but the mutant exhibited increased transformation efficiencies compared to <i>E. coli</i> DH5α for plasmids pUC19, pET-32a, and p1304, with enhancements of 2.23, 2.24, and 3.46 times, respectively. It was proved that <i>cspA</i> gene is an important negative regulatory gene in the CaCl<sub>2</sub> preparation of competent cells.</p></div>","PeriodicalId":15101,"journal":{"name":"Journal of Basic Microbiology","volume":"64 8","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jobm.202400113","citationCount":"0","resultStr":"{\"title\":\"Role of cspA on the Preparation of Escherichia coli Competent Cells by Calcium Chloride Method\",\"authors\":\"Xiaona Chen, Ning Zhu, Guangrui Yang, Xiaopeng Guo, Shangchen Sun, Feifan Leng, Yonggang Wang\",\"doi\":\"10.1002/jobm.202400113\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>One of the fundamental techniques in genetic engineering is the creation of <i>Escherichia coli</i> competent cells using the CaCl<sub>2</sub> method. However, little is known about the mechanism of <i>E. coli</i> competence formation. We have previously found that the <i>cspA</i> gene may play an indispensable role in the preparation of <i>E. coli</i> DH5α competent cells through multiomics analysis. In the present study, the cellular localization, physicochemical properties, and function of the protein expressed by the <i>cspA</i> gene were analyzed. To investigate the role of the <i>cspA</i> gene in <i>E. coli</i> transformation, <i>cspA-</i>deficient mutant was constructed by red homologous recombination. The growth, transformation efficiency, and cell morphology of the <i>cspA-</i>deficient strain and <i>E. coli</i> were compared. It was found that there were no noticeable differences in growth and morphology between <i>E. coli</i> and the <i>cspA-</i>deficient strain cultured at 37°C, but the mutant exhibited increased transformation efficiencies compared to <i>E. coli</i> DH5α for plasmids pUC19, pET-32a, and p1304, with enhancements of 2.23, 2.24, and 3.46 times, respectively. It was proved that <i>cspA</i> gene is an important negative regulatory gene in the CaCl<sub>2</sub> preparation of competent cells.</p></div>\",\"PeriodicalId\":15101,\"journal\":{\"name\":\"Journal of Basic Microbiology\",\"volume\":\"64 8\",\"pages\":\"\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2024-06-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jobm.202400113\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Basic Microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/jobm.202400113\",\"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.202400113","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Role of cspA on the Preparation of Escherichia coli Competent Cells by Calcium Chloride Method
One of the fundamental techniques in genetic engineering is the creation of Escherichia coli competent cells using the CaCl2 method. However, little is known about the mechanism of E. coli competence formation. We have previously found that the cspA gene may play an indispensable role in the preparation of E. coli DH5α competent cells through multiomics analysis. In the present study, the cellular localization, physicochemical properties, and function of the protein expressed by the cspA gene were analyzed. To investigate the role of the cspA gene in E. coli transformation, cspA-deficient mutant was constructed by red homologous recombination. The growth, transformation efficiency, and cell morphology of the cspA-deficient strain and E. coli were compared. It was found that there were no noticeable differences in growth and morphology between E. coli and the cspA-deficient strain cultured at 37°C, but the mutant exhibited increased transformation efficiencies compared to E. coli DH5α for plasmids pUC19, pET-32a, and p1304, with enhancements of 2.23, 2.24, and 3.46 times, respectively. It was proved that cspA gene is an important negative regulatory gene in the CaCl2 preparation of competent cells.
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).