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在莱茵衣藻叶绿体中表达 hemH 和 lba 基因提高了氢气的产量。

Improved hydrogen production with expression of hemH and lba genes in chloroplast of Chlamydomonas reinhardtii.

机构信息

Department of Biology, College of Life and Environmental Science, Shanghai Normal University, Guilin Road 100, Shanghai City 200234, China.

出版信息

J Biotechnol. 2010 Apr 1;146(3):120-5. doi: 10.1016/j.jbiotec.2010.01.023. Epub 2010 Feb 6.

Abstract

The coding region of both the ferrochelatase gene, hemH, from Bradyrhizobium japonicum, and the leghemoglobin gene, lba, from Glycine max, were transferred into chloroplast of Chlamydomonas reinhardtii. As a result, transgenic C. reinhardtii cultures more rapidly consumed O(2) and increased H(2) output compared with controls in both sulfur-free and sulfur-containing medium. H(2) production of the transgenic algal cultures in sulfur-free medium was 4-fold greater than that of control cultures, approximately 3.3mlbottle(-1). Maximum expression of the hemH-lba fusion protein on day 5 coincided with the lowest levels of O(2) content and the highest H(2) evolution rate detected over 7 days of anaerobic induction in sulfur-free medium. When the concentration of sulfate in the growth medium was restored to 12.5 or 50microM, O(2) consumption and H(2) yield decreased more slowly in the transgenic algal cultures than in the control cultures. These results demonstrate that expression of the hemH-lba fusion protein in chloroplast of C. reinhardtii improved their H(2) yield by decreasing O(2) content in the medium, thereby representing the potential for H(2) production in green algae to be improved.

摘要

亚铁螯合酶基因(hemH)来自日本根瘤菌和大豆血红蛋白基因(lba)均被转入莱茵衣藻的叶绿体中。结果,与对照相比,在无硫和含硫培养基中,转铁螯合酶基因莱茵衣藻培养物消耗 O(2)并增加 H(2)产量的速度更快。无硫培养基中转基因藻类培养物的 H(2)产量比对照高 4 倍,约为 3.3ml/瓶。在无硫培养基中厌氧诱导 7 天期间,hemH-lba 融合蛋白的最大表达量与检测到的 O(2)含量最低和 H(2)演化率最高的时间相对应。当生长培养基中硫酸盐的浓度恢复到 12.5 或 50μM 时,与对照相比,转基因为 algal 培养物中 O(2)的消耗和 H(2)的产量下降速度更慢。这些结果表明,hemH-lba 融合蛋白在莱茵衣藻叶绿体中的表达通过降低培养基中的 O(2)含量提高了它们的 H(2)产量,从而提高了绿藻产氢的潜力。

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