{"title":"携带衣藻异源电子供体铁氧体 1 的小球藻 DT 突变体的制氢能力","authors":"Yen-Ju Lin , Lee-Feng Chien","doi":"10.1016/j.ejbt.2024.03.001","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Ferredoxin 1 (Fd1) is the main electron donor to hydrogenase (HydA) for generating molecular hydrogen (H<sub>2</sub>) in green microalgae. In order to obtain an increased H<sub>2</sub> production, the Fd1 of <em>Chlamydomonas reinhardtii</em> (CrFd1, encoded by <em>crfd1</em>) was therefore overexpressed in <em>Chlorella</em> sp<em>.</em> DT (DT) in this study.</p></div><div><h3>Results</h3><p>The coding region of <em>crfd1</em> was constructed into the p121-crfd1 plasmid, which was also constructed with a resistance gene to the antibiotic geneticin (G418) as a selection marker. The p121-crfd1 plasmid was transformed into DT cells by electroporation. Observation of the <em>crfd1</em> gene fragment in the genomic DNA of DT-crfd1 mutants by PCR indicated that the transgene was successfully transformed. Using western blotting, the overexpressed CrFd1 protein, with a molecular weight of about 14 kDa, was found in DT-crfd1 mutants of DT-crfd1-4, DT-crfd1-22, and DT-crfd1-23. Using an <em>in vitro</em> assay, the H<sub>2</sub> production of DT-crfd1-4, DT-crfd1-22, and DT-crfd1-23 mutants was about 4.4-, 5.0-, and 3.8-fold higher, respectively, than the DT wild type (DT-WT). Using an <em>in vivo</em> assay, the H<sub>2</sub> production of DT-crfd1-4, DT-crfd1-22, and DT-crfd1-23 mutants was about 1.3-, 1.4-, and 1.2-fold higher, respectively, than the DT-WT.</p></div><div><h3>Conclusions</h3><p>The results suggested that heterologous overexpression of CrFd1 could enhance H<sub>2</sub> production in DT-crfd1 mutants even though <em>in vitro</em> H<sub>2</sub> production of DT-crfd1-22 mutant was up to 5-fold higher than the DT-WT.</p><p><strong>How to cite:</strong> Lin YJ, Chien LF. Hydrogen production in the <em>Chlorella</em> sp. DT mutants carrying heterologous electron donor ferredoxin 1 of <em>Chlamydomonas reinhardtii</em>. Electron J Biotechnol 2024;69. <span>https://doi.org/10.1016/j.ejbt.2024.03.001</span><svg><path></path></svg>.</p></div>","PeriodicalId":11529,"journal":{"name":"Electronic Journal of Biotechnology","volume":"69 ","pages":"Pages 11-20"},"PeriodicalIF":2.3000,"publicationDate":"2024-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0717345824000071/pdfft?md5=fc545c05fd113f1b9023ee7699c9f5ab&pid=1-s2.0-S0717345824000071-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Hydrogen production in the Chlorella sp. DT mutants carrying heterologous electron donor ferredoxin 1 of Chlamydomonas reinhardtii\",\"authors\":\"Yen-Ju Lin , Lee-Feng Chien\",\"doi\":\"10.1016/j.ejbt.2024.03.001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Ferredoxin 1 (Fd1) is the main electron donor to hydrogenase (HydA) for generating molecular hydrogen (H<sub>2</sub>) in green microalgae. In order to obtain an increased H<sub>2</sub> production, the Fd1 of <em>Chlamydomonas reinhardtii</em> (CrFd1, encoded by <em>crfd1</em>) was therefore overexpressed in <em>Chlorella</em> sp<em>.</em> DT (DT) in this study.</p></div><div><h3>Results</h3><p>The coding region of <em>crfd1</em> was constructed into the p121-crfd1 plasmid, which was also constructed with a resistance gene to the antibiotic geneticin (G418) as a selection marker. The p121-crfd1 plasmid was transformed into DT cells by electroporation. Observation of the <em>crfd1</em> gene fragment in the genomic DNA of DT-crfd1 mutants by PCR indicated that the transgene was successfully transformed. Using western blotting, the overexpressed CrFd1 protein, with a molecular weight of about 14 kDa, was found in DT-crfd1 mutants of DT-crfd1-4, DT-crfd1-22, and DT-crfd1-23. Using an <em>in vitro</em> assay, the H<sub>2</sub> production of DT-crfd1-4, DT-crfd1-22, and DT-crfd1-23 mutants was about 4.4-, 5.0-, and 3.8-fold higher, respectively, than the DT wild type (DT-WT). Using an <em>in vivo</em> assay, the H<sub>2</sub> production of DT-crfd1-4, DT-crfd1-22, and DT-crfd1-23 mutants was about 1.3-, 1.4-, and 1.2-fold higher, respectively, than the DT-WT.</p></div><div><h3>Conclusions</h3><p>The results suggested that heterologous overexpression of CrFd1 could enhance H<sub>2</sub> production in DT-crfd1 mutants even though <em>in vitro</em> H<sub>2</sub> production of DT-crfd1-22 mutant was up to 5-fold higher than the DT-WT.</p><p><strong>How to cite:</strong> Lin YJ, Chien LF. Hydrogen production in the <em>Chlorella</em> sp. DT mutants carrying heterologous electron donor ferredoxin 1 of <em>Chlamydomonas reinhardtii</em>. Electron J Biotechnol 2024;69. <span>https://doi.org/10.1016/j.ejbt.2024.03.001</span><svg><path></path></svg>.</p></div>\",\"PeriodicalId\":11529,\"journal\":{\"name\":\"Electronic Journal of Biotechnology\",\"volume\":\"69 \",\"pages\":\"Pages 11-20\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2024-04-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S0717345824000071/pdfft?md5=fc545c05fd113f1b9023ee7699c9f5ab&pid=1-s2.0-S0717345824000071-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Electronic Journal of Biotechnology\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0717345824000071\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electronic Journal of Biotechnology","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0717345824000071","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
Hydrogen production in the Chlorella sp. DT mutants carrying heterologous electron donor ferredoxin 1 of Chlamydomonas reinhardtii
Background
Ferredoxin 1 (Fd1) is the main electron donor to hydrogenase (HydA) for generating molecular hydrogen (H2) in green microalgae. In order to obtain an increased H2 production, the Fd1 of Chlamydomonas reinhardtii (CrFd1, encoded by crfd1) was therefore overexpressed in Chlorella sp. DT (DT) in this study.
Results
The coding region of crfd1 was constructed into the p121-crfd1 plasmid, which was also constructed with a resistance gene to the antibiotic geneticin (G418) as a selection marker. The p121-crfd1 plasmid was transformed into DT cells by electroporation. Observation of the crfd1 gene fragment in the genomic DNA of DT-crfd1 mutants by PCR indicated that the transgene was successfully transformed. Using western blotting, the overexpressed CrFd1 protein, with a molecular weight of about 14 kDa, was found in DT-crfd1 mutants of DT-crfd1-4, DT-crfd1-22, and DT-crfd1-23. Using an in vitro assay, the H2 production of DT-crfd1-4, DT-crfd1-22, and DT-crfd1-23 mutants was about 4.4-, 5.0-, and 3.8-fold higher, respectively, than the DT wild type (DT-WT). Using an in vivo assay, the H2 production of DT-crfd1-4, DT-crfd1-22, and DT-crfd1-23 mutants was about 1.3-, 1.4-, and 1.2-fold higher, respectively, than the DT-WT.
Conclusions
The results suggested that heterologous overexpression of CrFd1 could enhance H2 production in DT-crfd1 mutants even though in vitro H2 production of DT-crfd1-22 mutant was up to 5-fold higher than the DT-WT.
How to cite: Lin YJ, Chien LF. Hydrogen production in the Chlorella sp. DT mutants carrying heterologous electron donor ferredoxin 1 of Chlamydomonas reinhardtii. Electron J Biotechnol 2024;69. https://doi.org/10.1016/j.ejbt.2024.03.001.
期刊介绍:
Electronic Journal of Biotechnology is an international scientific electronic journal, which publishes papers from all areas related to Biotechnology. It covers from molecular biology and the chemistry of biological processes to aquatic and earth environmental aspects, computational applications, policy and ethical issues directly related to Biotechnology.
The journal provides an effective way to publish research and review articles and short communications, video material, animation sequences and 3D are also accepted to support and enhance articles. The articles will be examined by a scientific committee and anonymous evaluators and published every two months in HTML and PDF formats (January 15th , March 15th, May 15th, July 15th, September 15th, November 15th).
The following areas are covered in the Journal:
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