Sustainable bioproduction of the blue pigment indigoidine: Expanding the range of heterologous products in R. toruloides to include non-ribosomal peptides†

IF 9.3 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Green Chemistry Pub Date : 2019-05-28 DOI:10.1039/C9GC00920E
Maren Wehrs, John M. Gladden, Yuzhong Liu, Lukas Platz, Jan-Philip Prahl, Jadie Moon, Gabriella Papa, Eric Sundstrom, Gina M. Geiselman, Deepti Tanjore, Jay D. Keasling, Todd R. Pray, Blake A. Simmons and Aindrila Mukhopadhyay
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引用次数: 42

Abstract

Non-ribosomal peptides (NRPs) constitute a diverse class of valuable secondary metabolites, with potential industrial applications including use as pharmaceuticals, polymers and dyes. Current industrial production of dyes is predominantly achieved via chemical synthesis, which can involve toxic precursors and generate hazardous byproducts. Thus, alternative routes of dye production are highly desirable to enhance both workplace safety and environmental sustainability. Correspondingly, biological synthesis of dyes from renewable carbon would serve an ideal green chemistry paradigm. Therefore, we engineered the fungal host Rhodosporidium toruloides to produce the blue pigment indigoidine, an NRP with potential applications in the dye industry, using various low-cost carbon and nitrogen sources. To demonstrate production from renewable carbon sources and assess process scalability we produced indigoidine in 2 L bioreactors, reaching titers of 2.9 ± 0.8 g L?1 using a sorghum lignocellulosic hydrolysate in a batch process and 86.3 ± 7.4 g L?1 using glucose in a high-gravity fed-batch process. This study represents the first heterologous production of an NRP in R. toruloides, thus extending the range of microbial hosts that can be used for sustainable, heterologous production of NRPs. In addition, this is the first demonstration of producing an NRP using lignocellulose. These results highlight the potential of R. toruloides for the sustainable, and scalable production of NRPs, with the highest reported titer of indigoidine or any heterologously produced NRP to date.

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蓝色素靛蓝素的可持续生物生产:扩大红胸草属异源产物的范围,包括非核糖体肽†
非核糖体肽(nrp)是一类有价值的次级代谢物,具有潜在的工业应用,包括用作药物、聚合物和染料。目前染料的工业生产主要是通过化学合成来实现的,这可能涉及有毒的前体并产生有害的副产品。因此,染料生产的替代路线是非常可取的,以提高工作场所的安全和环境的可持续性。相应地,从可再生碳中生物合成染料将成为理想的绿色化学范例。因此,我们利用各种低成本的碳和氮源,对真菌宿主红孢子虫(Rhodosporidium toruloides)进行改造,以生产蓝色色素靛蓝素,这是一种在染料工业中具有潜在应用前景的NRP。为了演示可再生碳源的生产并评估工艺可扩展性,我们在2l生物反应器中生产靛蓝,滴度达到2.9±0.8 g L?1 .采用高粱木质纤维素水解物间歇式工艺,86.3±7.4 g L?在高重力间歇进料过程中使用葡萄糖。该研究首次在圆叶蝉中实现了NRP的异源生产,从而扩大了微生物宿主的范围,可用于可持续的、异源生产NRP。此外,这是第一次使用木质纤维素生产NRP的演示。这些结果突出了圆尾圆尾圆霉在可持续和规模化生产NRP方面的潜力,迄今为止报道的靛蓝素或任何异种生产的NRP滴度最高。
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来源期刊
Green Chemistry
Green Chemistry 化学-化学综合
CiteScore
16.10
自引率
7.10%
发文量
677
审稿时长
1.4 months
期刊介绍: Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.
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Back cover Back cover Electrochemical dehydrogenative annulation for the synthesis of 4-oxo-oxazolines† Retraction: Copper catalyzed direct C–H double methylation of aromatic aldehydes employing methanol as an alkylating agent Decatungstate-photocatalyzed tandem acylation/cyclization/self-hydrogenation of isocyanides with aldehydes to hydroxyalkylated N-heteroarenes via multiple hydrogen atom transfer†
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