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利用工程化蓝细菌直接从 CO2 光合生产 3-羟基丁酸。

Engineering cyanobacteria for photosynthetic production of 3-hydroxybutyrate directly from CO2.

机构信息

Center for Biosignatures Discovery Automation, The Biodesign Institute, Arizona State University, Tempe, AZ 85287-6501, USA.

出版信息

Metab Eng. 2013 Mar;16:68-77. doi: 10.1016/j.ymben.2013.01.001. Epub 2013 Jan 16.

Abstract

(S)- and (R)-3-hydroxybutyrate (3HB) are precursors to synthesize the biodegradable plastics polyhydroxyalkanoates (PHAs) and many fine chemicals. To date, however, their production has been restricted to petroleum-based chemical industry and sugar-based microbial fermentation, limiting its sustainability and economical feasibility. With the ability to fix CO2 photosynthetically, cyanobacteria have attracted increasing interest as a biosynthesis platform to produce fuels and chemicals from alternative renewable resources. To this end, synthesis metabolic pathways have been constructed and optimized in cyanobacterium Synechocystis sp. PCC 6803 to photosynthetically produce (S)- and (R)-3HB directly from CO2. Both types of 3HB molecules were produced and readily secreted from Synechocystis cells without over-expression of transporters. Additional inactivation of the competing pathway by deleting slr1829 and slr1830 (encoding PHB polymerase) from the Synechocystis genome further promoted the 3HB production. Up to 533.4mg/L 3HB has been produced after photosynthetic cultivation of the engineered cyanobacterium Synechocystis TABd for 21 days. Further analysis indicated that the phosphate consumption during the photoautrophic growth and the concomitant elevated acetyl-CoA pool acted as a key driving force for 3HB biosynthesis in Synechocystis. For the first time, the study has demonstrated the feasibility of photosynthetic production of (S)- and (R)-3HB directly from sunlight and CO2.

摘要

(S)-和(R)-3-羟基丁酸(3HB)是合成可生物降解塑料聚羟基烷酸酯(PHAs)和许多精细化学品的前体。然而,迄今为止,它们的生产一直局限于基于石油的化学工业和基于糖的微生物发酵,限制了其可持续性和经济可行性。由于具有固定 CO2 的光合作用能力,蓝藻作为生物合成平台,从替代可再生资源生产燃料和化学品,引起了越来越多的兴趣。为此,已在集胞藻 PCC 6803 中构建和优化了合成代谢途径,以从 CO2 光合成直接生产(S)-和(R)-3HB。这两种 3HB 分子都在没有过度表达转运蛋白的情况下在集胞藻细胞中产生并容易分泌。通过从集胞藻基因组中删除 slr1829 和 slr1830(编码 PHB 聚合酶)进一步抑制竞争途径,进一步促进了 3HB 的生产。经过工程化集胞藻 Synechocystis TABd 光合作用培养 21 天后,可生产出 533.4mg/L 的 3HB。进一步分析表明,在光自养生长过程中消耗的磷酸盐和同时升高的乙酰辅酶 A 池是集胞藻 3HB 生物合成的关键驱动力。该研究首次证明了从阳光和 CO2 直接光合成生产(S)-和(R)-3HB 的可行性。

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