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通过木糖生产柠檬烯的棉阿舒囊霉代谢工程。

Metabolic engineering of Ashbya gossypii for limonene production from xylose.

作者信息

Muñoz-Fernández Gloria, Martínez-Buey Rubén, Revuelta José Luis, Jiménez Alberto

机构信息

Metabolic Engineering Group, Department of Microbiology and Genetics, Universidad de Salamanca, Campus Miguel de Unamuno, 37007, Salamanca, Spain.

出版信息

Biotechnol Biofuels Bioprod. 2022 Jul 15;15(1):79. doi: 10.1186/s13068-022-02176-0.

Abstract

BACKGROUND

Limonene is a cyclic monoterpene that has applications in the food, cosmetic, and pharmaceutical industries. The industrial production of limonene and its derivatives through plant extraction presents important drawbacks such as seasonal and climate issues, feedstock limitations, low efficiency and environmental concerns. Consequently, the implementation of efficient and eco-friendly bioprocesses for the production of limonene and other terpenes constitutes an attractive goal for microbial biotechnology. In this context, novel biocatalysts with the ability to produce limonene from alternative carbon sources will help to meet the industrial demands of limonene.

RESULTS

Engineered strains of the industrial fungus Ashbya gossypii have been developed to produce limonene from xylose. The limonene synthase (LS) from Citrus limon was initially overexpressed together with the native HMG1 gene (coding for HMG-CoA reductase) to establish a limonene-producing platform from a xylose-utilizing A. gossypii strain. In addition, several strategies were designed to increase the production of limonene. Hence, the effect of mutant alleles of ERG20 (erg20 and erg20) were evaluated together with a synthetic orthogonal pathway using a heterologous neryl diphosphate synthase. The lethality of the A. gossypii double mutant erg20 highlights the indispensability of farnesyl diphosphate for the synthesis of essential sterols. In addition, the utilization of the orthogonal pathway, bypassing the Erg20 activity through neryl diphosphate, triggered a substantial increase in limonene titer (33.6 mg/L), without critically altering the fitness of the engineered strain. Finally, the overexpression of the native ERG12 gene further enhanced limonene production, which reached 336.4 mg/L after 96 h in flask cultures using xylose as the carbon source.

CONCLUSIONS

The microbial production of limonene can be carried out using engineered strains of A. gossypii from xylose-based carbon sources. The utilization of a synthetic orthogonal pathway together with the overexpression of ERG12 is a highly beneficial strategy for the production of limonene in A. gossypii. The strains presented in this work constitute a proof of principle for the production of limonene and other terpenes from agro-industrial wastes such as xylose-rich hydrolysates in A. gossypii.

摘要

背景

柠檬烯是一种环状单萜,在食品、化妆品和制药行业有应用。通过植物提取进行柠檬烯及其衍生物的工业生产存在重要缺陷,如季节性和气候问题、原料限制、效率低下以及环境问题。因此,实施高效且环保的生物工艺来生产柠檬烯和其他萜类化合物是微生物生物技术的一个有吸引力的目标。在这种背景下,具有从替代碳源生产柠檬烯能力的新型生物催化剂将有助于满足柠檬烯的工业需求。

结果

已开发出工业真菌棉阿舒囊霉的工程菌株,用于从木糖生产柠檬烯。最初将来自柠檬的柠檬烯合酶(LS)与天然HMG1基因(编码HMG-CoA还原酶)一起过表达,以建立一个利用木糖的棉阿舒囊霉菌株生产柠檬烯的平台。此外,还设计了几种策略来提高柠檬烯的产量。因此,评估了ERG20突变等位基因(erg20和erg20)的效果,并使用异源香叶基二磷酸合酶构建了一条合成正交途径。棉阿舒囊霉双突变体erg20的致死性突出了法呢基二磷酸对于必需甾醇合成的不可或缺性。此外,利用正交途径,通过香叶基二磷酸绕过Erg20活性,引发了柠檬烯产量的大幅增加(33.6 mg/L),而没有严重改变工程菌株的适应性。最后,天然ERG12基因的过表达进一步提高了柠檬烯产量,在以木糖为碳源的摇瓶培养中培养96小时后,产量达到336.4 mg/L。

结论

可以使用棉阿舒囊霉的工程菌株从基于木糖的碳源进行柠檬烯的微生物生产。利用合成正交途径以及ERG12的过表达是在棉阿舒囊霉中生产柠檬烯的一种非常有益的策略。这项工作中展示的菌株构成了利用棉阿舒囊霉从富含木糖的水解产物等农业工业废物生产柠檬烯和其他萜类化合物的原理证明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77de/9284773/bc8b49521426/13068_2022_2176_Fig1_HTML.jpg

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