Key Laboratory of Food Nutrition and Safety (Tianjin University of Science & Technology), Ministry of Education, Tianjin, 300457, China.
Beijing Advanced Innovation Center for Food Nutrition and Human Health, Beijing Technology & Business University (BTBU), Beijing, 100048, China.
Appl Microbiol Biotechnol. 2017 Oct;101(19):7281-7292. doi: 10.1007/s00253-017-8462-7. Epub 2017 Aug 22.
As traditional edible fungi, Monascus spp. have been widely used as folk medicine, food colorants, and fermentation starters in East Asian countries for more than a thousand years. However, the presence of citrinin, which has nephrotoxic, hepatotoxic, and carcinogenic activities, raises suspicions about the safety of Monascus products. Citrinin biosynthesis in Monascus is known to occur via a polyketide pathway and a citrinin biosynthesis gene cluster, which include the characterized polyketide synthetase pksCT. A gene, orf6, encodes a protein that shows significant similarity to glyoxalase and is located between ctnE and orf1. This study analyzed orf6 function, and successfully obtained an orf6 disruption strain (Δorf6). Citrinin production was significantly greater (3.6-fold) in the Δorf6 strain than in the wild-type Monascus purpureus YY-1, and RT-PCR analysis further revealed increased expression of numerous genes of the citrinin biosynthesis gene cluster in Δorf6. Therefore, orf6 proved to be a major inhibitor, directly involved in citrinin biosynthesis. Moreover, pigment production in Δorf6 was reduced by approximately 30%, while the transcription levels of many genes involved in Monascus pigments (MPs) biosynthesis had increased. This dichotomy indicated that MPs and citrinin yields may be improved simultaneously; however, a portion of the pigments was consumed to protect the cells from oxidative damage in the Δorf6 strain. An Δorf6 revertant restored the citrinin and pigment yields to normal levels. This study makes a contribution to explore the citrinin biosynthesis pathway and provides some theoretical guidance to improving the safety of Monascus-related products.
作为传统的食用真菌,红曲菌已在东亚国家被广泛用作民间药物、食品着色剂和发酵剂,使用历史已超过千年。然而,桔霉素的存在引起了人们对红曲产品安全性的怀疑,因为桔霉素具有肾毒性、肝毒性和致癌性。桔霉素在红曲中的生物合成途径是众所周知的,它涉及聚酮化合物途径和桔霉素生物合成基因簇,其中包括特征性的聚酮合酶 pksCT。一个基因 orf6 编码的蛋白质与乙醛酸酶有显著的相似性,位于 ctnE 和 orf1 之间。本研究分析了 orf6 的功能,并成功获得了一个 orf6 缺失菌株(Δorf6)。Δorf6 菌株的桔霉素产量比野生型 Monascus purpureus YY-1 显著增加(3.6 倍),RT-PCR 分析进一步显示,Δorf6 中桔霉素生物合成基因簇的许多基因表达水平增加。因此,orf6 被证明是桔霉素生物合成的主要抑制剂,直接参与桔霉素的生物合成。此外,Δorf6 中色素的产量降低了约 30%,而参与红曲色素(MPs)生物合成的许多基因的转录水平增加。这种二分法表明,MPs 和桔霉素的产量可能同时提高;然而,一部分色素被消耗,以保护细胞免受 Δorf6 菌株的氧化损伤。Δorf6 的回复突变体将桔霉素和色素的产量恢复到正常水平。本研究为探索桔霉素生物合成途径做出了贡献,并为提高与红曲相关产品的安全性提供了一些理论指导。