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肽介导的海洋紫色光合细菌的基因转移。

Peptide-Mediated Gene Transfer into Marine Purple Photosynthetic Bacteria.

机构信息

Biomacromolecules Research Team, RIKEN Center for Sustainable Resource Science, 2-1, Hirosawa, Wako-shi, Saitama 351-0198, Japan.

Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyoto-Daigaku-Katsura, Nishikyo-ku, Kyoto 615-8510, Japan.

出版信息

Int J Mol Sci. 2020 Nov 16;21(22):8625. doi: 10.3390/ijms21228625.

Abstract

Use of photosynthetic organisms is one of the sustainable ways to produce high-value products. Marine purple photosynthetic bacteria are one of the research focuses as microbial production hosts. Genetic transformation is indispensable as a biotechnology technique. However, only conjugation has been determined to be an applicable method for the transformation of marine purple photosynthetic bacteria so far. In this study, for the first time, a dual peptide-based transformation method combining cell penetrating peptide (CPP), cationic peptide and Tat-derived peptide (dTat-Sar-EED) (containing D-amino acids of Tat and endosomal escape domain (EED) connected by sarcosine linkers) successfully delivered plasmid DNA into a marine purple photosynthetic bacterium. The plasmid delivery efficiency was greatly improved by dTat-Sar-EED. The concentrations of dTat-Sar-EED, cell growth stage and recovery duration affected the efficiency of plasmid DNA delivery. The delivery was inhibited at 4 °C and by A22, which is an inhibitor of the actin homolog MreB. This suggests that the plasmid DNA delivery occurred via MreB-mediated energy dependent process. Additionally, this peptide-mediated delivery method was also applicable for cells. Thus, a wide range of bacteria could be genetically transformed by using this novel peptide-based transformation method.

摘要

利用光合生物是生产高价值产品的可持续方法之一。海洋紫色光合细菌是微生物生产宿主的研究重点之一。遗传转化是生物技术中不可或缺的一项技术。然而,到目前为止,只有接合被确定为海洋紫色光合细菌转化的一种适用方法。在这项研究中,首次结合细胞穿透肽(CPP)、阳离子肽和 Tat 衍生肽(dTat-Sar-EED)(含有 Tat 的 D-氨基酸和通过肌氨酸接头连接的内体逃逸结构域(EED))的双肽基转化方法成功地将质粒 DNA 递送至海洋紫色光合细菌中。dTat-Sar-EED 大大提高了质粒的递送效率。dTat-Sar-EED 的浓度、细胞生长阶段和恢复时间都会影响质粒 DNA 的递送效率。在 4°C 和 A22(肌动蛋白同源物 MreB 的抑制剂)存在下,递送被抑制。这表明质粒 DNA 的递送是通过 MreB 介导的能量依赖过程发生的。此外,这种肽介导的递送方法也适用于 细胞。因此,这种新型的肽基转化方法可用于广泛的细菌的遗传转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83c2/7697693/040b85718219/ijms-21-08625-g001.jpg

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