Hydrogen production in the Chlorella sp. DT mutants carrying heterologous electron donor ferredoxin 1 of Chlamydomonas reinhardtii

IF 2.3 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yen-Ju Lin , Lee-Feng Chien
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引用次数: 0

Abstract

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.

Abstract Image

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
背景Ferredoxin 1(Fd1)是绿色微藻中氢化酶(HydA)的主要电子供体,用于产生分子氢(H2)。为了提高 H2 的产量,本研究在小球藻 DT(DT)中过量表达了衣藻的 Fd1(CrFd1,由 crfd1 编码)。结果将 crfd1 的编码区构建到 p121-crfd1 质粒中,同时构建了抗生素基因素(G418)的抗性基因作为选择标记。通过电穿孔将 p121-crfd1 质粒转化到 DT 细胞中。通过 PCR 在 DT-crfd1 突变体的基因组 DNA 中观察到 crfd1 基因片段,表明转基因已成功转化。通过 Western 印迹法,在 DT-crfd1-4、DT-crfd1-22 和 DT-crfd1-23 突变体中发现了过表达的 CrFd1 蛋白,分子量约为 14 kDa。通过体外检测,DT-crfd1-4、DT-crfd1-22 和 DT-crfd1-23 突变体的 H2 产量分别比 DT 野生型(DT-WT)高出约 4.4、5.0 和 3.8 倍。通过体内检测,DT-crfd1-4、DT-crfd1-22和DT-crfd1-23突变体的H2产生量分别比DT-WT高出约1.3倍、1.4倍和1.2倍。结论结果表明,异源过表达CrFd1可提高DT-crfd1突变体的H2产生量,尽管DT-crfd1-22突变体的体外H2产生量比DT-WT高出达5倍:Lin YJ, Chien LF.携带衣藻异源电子供体铁氧体1的小球藻DT突变体的产氢量。Electron J Biotechnol 2024;69. https://doi.org/10.1016/j.ejbt.2024.03.001.
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来源期刊
Electronic Journal of Biotechnology
Electronic Journal of Biotechnology 工程技术-生物工程与应用微生物
CiteScore
5.60
自引率
0.00%
发文量
50
审稿时长
2 months
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: • Animal Biotechnology • Biofilms • Bioinformatics • Biomedicine • Biopolicies of International Cooperation • Biosafety • Biotechnology Industry • Biotechnology of Human Disorders • Chemical Engineering • Environmental Biotechnology • Food Biotechnology • Marine Biotechnology • Microbial Biotechnology • Molecular Biology and Genetics •Nanobiotechnology • Omics • Plant Biotechnology • Process Biotechnology • Process Chemistry and Technology • Tissue Engineering
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