用工程学方法生产海洋拟南芥二萜化合物

mLife Pub Date : 2023-12-26 DOI:10.1002/mlf2.12097
Zhi‐Yan Du, Wajid W. Bhat, Eric Poliner, Sean Johnson, Conor Bertucci, Eva Farre, B. Hamberger
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引用次数: 0

摘要

光合微藻(如拟南芥)作为可持续的光驱动生物工厂,在生产高价值天然产品(如萜类化合物)方面具有巨大潜力。Nannochloropsis oceanica 是一种特别强健的宿主,拥有广泛的基因组和转基因资源。它能够在废水、咸水和海水中生长,再加上微藻代谢工程、基因组编辑和合成生物学的进步,为其提供了一个绝佳的机会。在本研究中,我们展示了如何设计海洋藻来生产二萜类化合物 Casbene--药用大环二萜生物合成过程中的一种重要中间体。将来自 Daphne genkwa(DgTPS1)的腰果烯合成酶稳定表达并靶向到藻类叶绿体后,腰果烯得以积累。改造后的菌株可产生滴度高达 0.12 mg g-1 的总干细胞重量(DCW)的 Casbene。2-C-甲基-d-赤藓糖醇-4-磷酸途径中的两个上游限速酶--Coleus forskohlii 1-deoxy-d-xylulose-5-phosphate合酶和geranylgeranyl diphosphate合酶基因的异源过表达和叶绿体靶向,进一步提高了 casbene 的产量,滴度高达 1.80 mg g-1 DCW。本文介绍的结果为进一步在微藻中开发和生产复杂的植物二萜奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Engineering Nannochloropsis oceanica for the production of diterpenoid compounds
Photosynthetic microalgae like Nannochloropsis hold enormous potential as sustainable, light‐driven biofactories for the production of high‐value natural products such as terpenoids. Nannochloropsis oceanica is distinguished as a particularly robust host with extensive genomic and transgenic resources available. Its capacity to grow in wastewater, brackish, and sea waters, coupled with advances in microalgal metabolic engineering, genome editing, and synthetic biology, provides an excellent opportunity. In the present work, we demonstrate how N. oceanica can be engineered to produce the diterpene casbene—an important intermediate in the biosynthesis of pharmacologically relevant macrocyclic diterpenoids. Casbene accumulated after stably expressing and targeting the casbene synthase from Daphne genkwa (DgTPS1) to the algal chloroplast. The engineered strains yielded production titers of up to 0.12 mg g−1 total dry cell weight (DCW) casbene. Heterologous overexpression and chloroplast targeting of two upstream rate‐limiting enzymes in the 2‐C‐methyl‐d‐erythritol 4‐phosphate pathway, Coleus forskohlii 1‐deoxy‐d‐xylulose‐5‐phosphate synthase and geranylgeranyl diphosphate synthase genes, further enhanced the yield of casbene to a titer up to 1.80 mg g−1 DCW. The results presented here form a basis for further development and production of complex plant diterpenoids in microalgae.
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