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通过蓝藻酰基-ACP/CoA还原酶和醛脱甲酰基加氧酶基因的异源表达,黑曲霉ITEM 5010合成烷烃

Alkane biosynthesis by Aspergillus carbonarius ITEM 5010 through heterologous expression of Synechococcus elongatus acyl-ACP/CoA reductase and aldehyde deformylating oxygenase genes.

作者信息

Sinha Malavika, Weyda István, Sørensen Annette, Bruno Kenneth S, Ahring Birgitte K

机构信息

Bioproducts, Sciences and Engineering Laboratory, Washington State University, 2710 Crimson Way, Richland, WA, 99354, USA.

Section for Sustainable Biotechnology, Aalborg University Copenhagen, AC Meyers Vaenge 15, 2450, Copenhagen SV, Denmark.

出版信息

AMB Express. 2017 Dec;7(1):18. doi: 10.1186/s13568-016-0321-x. Epub 2017 Jan 5.

Abstract

In this study we describe the heterologous expression of the recently identified cyanobacterial pathway for long chain alkane biosynthesis, involving the reduction of fatty acyl-ACP to fatty aldehyde and the subsequent conversion of this into alkanes, in the filamentous fungus Aspergillus carbonarius ITEM 5010. Genes originating from Synechococcus elongatus strain PCC7942, encoding acyl-ACP/CoA reductase and aldehyde deformylating oxygenase enzymes, were successfully expressed in A. carbonarius, which lead to the production of pentadecane and heptadecane, alkanes that have not been previously produced by this fungus. Titers of 0.2, 0.5 and 2.7 mg/l pentadecane and 0.8, 1.6 and 10.2 mg/l heptadecane were achieved using glucose, Yeast malt and oatmeal media, respectively. Besides producing alkanes, we found elevated levels of internal free fatty acids and triglycerides in the alkane producing transformant. These findings can indicate that a yet unidentified, native fatty aldehyde dehydrogenase channels back the fatty aldehydes into the fatty acid metabolism, thus competing for substrate with the heterologously expressed fatty aldehyde deformylating oxygenase. These findings will potentially facilitate the future application of robust, fungal cell factories for the production of advanced biofuels from various substrates.

摘要

在本研究中,我们描述了丝状真菌黑曲霉ITEM 5010中最近鉴定出的蓝藻长链烷烃生物合成途径的异源表达,该途径涉及将脂肪酰基-ACP还原为脂肪醛,并随后将其转化为烷烃。源自聚球藻菌株PCC7942的编码酰基-ACP/CoA还原酶和醛脱甲酰基加氧酶的基因在黑曲霉中成功表达,这导致了十五烷和十七烷的产生,这两种烷烃此前未曾由该真菌产生过。分别使用葡萄糖、酵母麦芽和燕麦培养基时,十五烷的产量达到了0.2、0.5和2.7毫克/升,十七烷的产量达到了0.8、1.6和10.2毫克/升。除了产生烷烃外,我们还发现产烷烃转化体中内部游离脂肪酸和甘油三酯的水平升高。这些发现可能表明,一种尚未鉴定的天然脂肪醛脱氢酶将脂肪醛重新导向脂肪酸代谢,从而与异源表达的醛脱甲酰基加氧酶争夺底物。这些发现可能会促进未来利用强大的真菌细胞工厂从各种底物生产先进生物燃料的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94f2/5216010/d50d2efb0c19/13568_2016_321_Fig1_HTML.jpg

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