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Heterologous production of the widely used natural food colorant carminic acid in Aspergillus nidulans

机译:在构巢曲霉中异源生产广泛使用的天然食用色素胭脂红酸

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摘要

The natural red food colorants carmine (E120) and carminic acid are currently produced from scale insects. The access to raw material is limited and current production is sensitive to fluctuation in weather conditions. A cheaper and more stable supply is therefore desirable. Here we present the first proof-of-concept of heterologous microbial production of carminic acid in Aspergillus nidulans by developing a semi-natural biosynthetic pathway. Formation of the tricyclic core of carminic acid is achieved via a two-step process wherein a plant type III polyketide synthase (PKS) forms a non-reduced linear octaketide, which subsequently is folded into the desired flavokermesic acid anthrone (FKA) structure by a cyclase and a aromatase from a bacterial type II PKS system. The formed FKA is oxidized to flavokermesic acid and kermesic acid, catalyzed by endogenous A. nidulans monooxygenases, and further converted to dcII and carminic acid by the Dactylopius coccus C-glucosyltransferase DcUGT2. The establishment of a functional biosynthetic carminic acid pathway in A. nidulans serves as an important step towards industrial-scale production of carminic acid via liquid-state fermentation using a microbial cell factory.
机译:天然红色食用色素胭脂红(E120)和胭脂红酸目前是由鳞片昆虫生产的。原材料的获取受到限制,当前的生产对天气状况的波动非常敏感。因此,需要更便宜和更稳定的供应。在这里,我们通过开发半自然的生物合成途径,提出了构巢曲霉中氨基甲酸异源微生物生产的第一个概念证明。氨基甲酸的三环核心的形成是通过两步过程实现的,其中植物III型聚酮化合物合酶(PKS)形成非还原的线性octaketide,随后将其折叠成所需的黄酮甲酸酯蒽酮(FKA)结构。细菌II型PKS系统的环化酶和芳香酶。形成的FKA被内源性构巢曲霉单加氧酶催化氧化为黄酮酸和角酮酸,并通过球菌球菌C-葡萄糖基转移酶DcUGT2进一步转化为dcII和胭脂酸。在构巢曲霉中建立功能性生物合成胭脂红酸途径是迈向通过微生物细胞工厂通过液态发酵工业规模生产胭脂红的重要步骤。

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