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利用重组微藻生产木糖醇。

Production of xylitol by recombinant microalgae.

机构信息

Department of Chemical Engineering, The University of Tulsa, 800 S. Tucker Drive, Tulsa, OK 74104, USA.

出版信息

J Biotechnol. 2013 Jun 10;165(3-4):178-83. doi: 10.1016/j.jbiotec.2013.04.002. Epub 2013 Apr 15.

Abstract

Microalgae have received significant attention recently as a potential low-cost host for the production of next-generation biofuels and natural products. Here we show that the chloroplast genome of the eukaryotic green microalga Chlamydomonas reinhardtii can be genetically engineered to produce xylitol through the introduction of a gene encoding a xylose reductase (XR) from the fungi Neurospora crassa. Increased levels of heterologous protein accumulation and xylitol production were achieved by synthesizing the XR gene in the chloroplast codon bias and by driving expression of the codon-optimized XR gene using a 16S/atpA promoter/5'-UTR fusion. These results demonstrate the feasibility of engineering microalgae to produce xylitol, and show the importance of codon optimizing the XR gene and using the 16S/atpA promoter/5'-UTR fusion to express XR in the chloroplast of C. reinhardtii.

摘要

最近,微藻作为生产下一代生物燃料和天然产物的潜在低成本宿主受到了广泛关注。在这里,我们展示了可以通过引入来自真菌粗糙脉孢菌的木糖还原酶(XR)基因,对真核绿藻莱茵衣藻的叶绿体基因组进行基因工程改造,以生产木糖醇。通过在叶绿体密码子偏好性中合成 XR 基因,并使用 16S/atpA 启动子/5'-UTR 融合驱动密码子优化的 XR 基因表达,实现了异源蛋白积累和木糖醇产量的增加。这些结果证明了对微藻进行工程改造以生产木糖醇的可行性,并表明了对 XR 基因进行密码子优化以及在 C. reinhardtii 的叶绿体中使用 16S/atpA 启动子/5'-UTR 融合来表达 XR 的重要性。

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