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利用光和表达酶mFMO的重组聚球藻属PCC6803菌株实现靛蓝生产的绿色化

Greening the Production of Indigo Blue Exploiting Light and a Recombinant Synechocystis sp. PCC6803 Strain Expressing the Enzyme mFMO.

作者信息

Loprete Giovanni, Rubert David, Bellusci Francesco, Lončar Nikola, Fraaije Marco W, Bergantino Elisabetta

机构信息

Synthetic Biology and Biotechnology Unit, Department of Biology, University of Padova, Padova, Italy.

Gecco Biotech, Groningen, the Netherlands.

出版信息

Microb Biotechnol. 2025 May;18(5):e70146. doi: 10.1111/1751-7915.70146.

Abstract

Cyanobacteria are emerging as interesting cell factories, offering the significant advantage of their in-built photosynthetic machinery, which generates NADPH to support redox biocatalysis. In this study, we assessed the potential of the cyanobacterium Synechocystis sp. PCC6803 in producing the dye indigo by light-driven whole-cell biotransformation using indole as a starting compound. A stable transgenic strain expressing a flavin-containing monooxygenase from Methylophaga aminisulfidivorans (mFMO) was engineered, enabling light-dependent indigo production. Upon optimising conditions, effective biotransformations could be performed, resulting in 112 mg/L indigo (86% conversion of the furnished indole). Additionally, we present a method for the recovery of the secreted dye directly from the growth medium through solid-phase absorption on polyamide nets. Overall, the effectiveness and sustainability of the biotransformation in Synechocystis sp. PCC6803 performed at the laboratory scale provide a strong basis for further exploring the applicability of the process.

摘要

蓝藻正成为引人关注的细胞工厂,其内置的光合机制具有显著优势,能产生NADPH以支持氧化还原生物催化。在本研究中,我们评估了聚球藻属蓝藻PCC6803以吲哚为起始化合物通过光驱动全细胞生物转化生产染料靛蓝的潜力。构建了一种稳定的转基因菌株,该菌株表达来自嗜氨基硫化甲基菌的含黄素单加氧酶(mFMO),从而实现了依赖光的靛蓝生产。在优化条件后,可以进行有效的生物转化,产生112毫克/升的靛蓝(所提供吲哚的转化率为86%)。此外,我们还提出了一种通过聚酰胺网固相吸附直接从生长培养基中回收分泌染料的方法。总体而言,在实验室规模下聚球藻属蓝藻PCC6803中生物转化的有效性和可持续性为进一步探索该工艺的适用性提供了有力依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/526e/12035870/6d3695e18e29/MBT2-18-e70146-g004.jpg

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