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Genetic manipulation of the bifunctional gene, carRA, to enhance lycopene content in Blakeslea trispora

Author:
Wang, Yanlong, Pang, Jing, Zheng, Yingmei, Jiang, Pingping, Gong, Wenfang, Chen, Xiwen, Chen, Defu
Source:
Biochemical engineering journal 2017 v.119 pp. 27-33
ISSN:
1369-703X
Subject:
Blakeslea trispora, beta-carotene, ergosterol, fermentation, gene expression regulation, gene overexpression, genes, genetic engineering, lycopene, phytoene synthase, quantitative polymerase chain reaction, reverse transcriptase polymerase chain reaction
Abstract:
Blakeslea trispora is an ideal natural source of lycopene. Here, we genetically manipulated the bifunctional protein gene, carRA, encoding a phytoene synthase and lycopene cyclase, to enhance lycopene production. carR- and carRA-knockout and carA overexpressing strains were obtained after several rounds of selection. Following combinational fermentation for 6 d, the lycopene content in carR-knockout strains increased from 0.47 to 1.40mg/gDW, while the total carotenoid content decreased from 17.05 to 3.52mg/gDW compared to the wild type. No carotenoid was produced in carRA-knockout strains. In carA overexpressing strains, lycopene content, β-carotene, and total carotenoid content increased 2.26-, 1.98-, and 2.02-fold, resepectively, with proportions similar to wild type. Dry weight increased 1.89–1.98-fold in carR- and carRA-knockout strains compared to the wild type, but not in carA overexpressing strains. qRT-PCR analysis revealed that disruption of CarR and CarRA down-regulated carotenoid synthesis genes, especially the isopentenyl pyrophosphate isomerase gene, whereas overexpression of carA up-regulated all examined genes, except the ergosterol synthase and the 4-hydroxybenzoate polyprenyl transferase genes. Tripropylamine was shown to target the R domain, rather than the A domain, of CarRA. Furthermore, the possibility of using a carR-knockout to obtain high-lycopene B. trispora strains for industrial production was explored.
Agid:
5628805