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Published on: September 12, 2018
Identification and role analysis of an intermediate produced by a polygenic mutant of Monascus pigments cluster in
Jiao Liu1, Youxiang Zhou2, Tao Yi1
1College of Food Science and Technology, Huazhong Agricultural University, Wuhan, 430070, China.
Abstract:
Monascus pigments (Mps) are a group of azaphilonic secondary metabolites produced by Monascus spp. via a polyketide pathway. A mutant deleted an about 30 kb region of Mps gene cluster from Monascus ruber M7 was isolated previously, which produces a high amount of a light yellow pigment. The current study revealed that the mutant named ΔMpigJ-R lost proximate eight genes of the Mps gene cluster in M. ruber M7 through genetic analysis at DNA and RNA levels. The produced light yellow material was identified as a benzaldehyde derivative named as 6-(4-hydroxy-2-oxopentyl)-3-methyl-2, 4-dioxocyclohexane carb-aldehyde (M7PKS-1) by FT-IR, NMR, and MS. The sodium acetate-1-(13)C feeding experiment indicated that M7PKS-1 was a product produced from polyketide pathway. Finally, the feeding of M7PKS-1 helped to induce and regain Mps production of the mutants (ΔMpigA and ΔMpigE) which were previously unable to biosynthesize Mps and proved that M7PKS-1 was an initial intermediate of Mps. The results in this study provide a line of action to unveil Monascus pigments biosynthesis pathway.
Insights
Researchers identified a new intermediate, M7PKS-1, in the biosynthesis of Monascus pigments (Mps). This discovery provides a pathway to understanding the complex Monascus pigments production process.
Area of Science:
- Microbiology
- Biochemistry
- Metabolic Engineering
Background:
- Monascus pigments (Mps) are valuable azaphilone metabolites produced by Monascus fungi.
- Understanding the Mps biosynthesis pathway is crucial for optimizing pigment production.
Purpose of the Study:
- To identify the light yellow pigment produced by a Monascus ruber M7 mutant (ΔMpigJ-R).
- To elucidate the role of this pigment as an intermediate in Monascus pigment biosynthesis.
Main Methods:
- Genetic analysis (DNA and RNA) of the Mps gene cluster in M. ruber M7.
- Spectroscopic identification (FT-IR, NMR, MS) of the pigment.
- Metabolic feeding experiments using sodium acetate-(13)C and the identified pigment.
Main Results:
- The mutant ΔMpigJ-R lost eight genes from the Mps gene cluster.
- The light yellow pigment was identified as 6-(4-hydroxy-2-oxopentyl)-3-methyl-2, 4-dioxocyclohexane carb-aldehyde (M7PKS-1).
- M7PKS-1 is a polyketide pathway product and an initial intermediate that can restore Mps production in other mutants.
Conclusions:
- M7PKS-1 is a key initial intermediate in Monascus pigment biosynthesis.
- This finding offers a strategy for further unraveling the Monascus pigment pathway.
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