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通过共表达葡聚糖酶和β-葡萄糖苷酶构建纤维素代谢的 Komagataella phaffii(巴斯德毕赤酵母)。

Construction of a cellulose-metabolizing Komagataella phaffii (Pichia pastoris) by co-expressing glucanases and β-glucosidase.

机构信息

Agency for Sciences, Technology and Research (A*STAR), Institute of Chemical and Engineering Sciences, 1 Pesek Road, Jurong Island, 627833, Singapore.

Institute of Molecular Biotechnology, Graz University of Technology, Petersgasse 14, 8010, Graz, Austria.

出版信息

Appl Microbiol Biotechnol. 2018 Feb;102(3):1297-1306. doi: 10.1007/s00253-017-8656-z. Epub 2017 Dec 4.

Abstract

Cellulose is a highly available and renewable carbon source in nature. However, it cannot be directly metabolized by most microbes including Komagataella phaffii (formerly Pichia pastoris), which is a frequently employed host for heterologous protein expression and production of high-value compounds. A K. phaffii strain was engineered that constitutively co-expresses an endoglucanase and a β-glucosidase both from Aspergillus niger and an exoglucanase from Trichoderma reesei under the control of bidirectional promoters. This engineered strain was able to grow on cellobiose and carboxymethyl cellulose (CMC) but not on Avicel. However, the detected release of cellobiose from Avicel by using the produced mixture of endoglucanase and exoglucanase as well as the released glucose from Avicel by using the produced mixture of all three cellulases at 50 °C indicated the production of exoglucanase under the liquid culture conditions. The successful expression of three cellulases in K. phaffii demonstrated the feasibility to enable K. phaffii to directly use cellulose as a carbon source for producing recombinant proteins or other high-value compounds.

摘要

纤维素是自然界中一种高可用性和可再生的碳源。然而,它不能被大多数微生物直接代谢,包括 Komagataella phaffii(以前称为 Pichia pastoris),它是用于异源蛋白表达和生产高价值化合物的常用宿主。构建了一株毕赤酵母工程菌株,该菌株组成型共表达来自黑曲霉的内切葡聚糖酶和β-葡萄糖苷酶,以及里氏木霉的外切葡聚糖酶,受双向启动子的控制。该工程菌株能够在纤维二糖和羧甲基纤维素(CMC)上生长,但不能在微晶纤维素(Avicel)上生长。然而,使用所产生的内切葡聚糖酶和外切葡聚糖酶混合物从微晶纤维素中检测到的纤维二糖的释放,以及使用三种纤维素酶的混合物在 50°C 下从微晶纤维素中释放的葡萄糖表明,外切葡聚糖酶是在液体培养条件下产生的。在毕赤酵母中成功表达三种纤维素酶表明,使毕赤酵母能够直接将纤维素用作生产重组蛋白或其他高价值化合物的碳源是可行的。

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