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Flavonoid Synthesis by Deinococcus sp. 43 Isolated from the Ginkgo Rhizosphere

Flavonoids are crucial in physiological and pharmaceutical processes, especially the treatment of cancer and the prevention of cardiovascular and cerebrovascular diseases. Flavonoid-producing plants and fungi have been extensively reported, but bacteria have been much less investigated as a source o...

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Autores principales: Zhou, Jin, Zou, Kai, Fu, Shaodong, Duan, Zhenchun, Zhang, Guoqing, Wu, Xinhong, Huang, Jingwen, Li, Shihui, Liu, Xueduan, Zhang, Shuangfei, Liang, Yili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10386165/
https://www.ncbi.nlm.nih.gov/pubmed/37513020
http://dx.doi.org/10.3390/microorganisms11071848
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author Zhou, Jin
Zou, Kai
Fu, Shaodong
Duan, Zhenchun
Zhang, Guoqing
Wu, Xinhong
Huang, Jingwen
Li, Shihui
Liu, Xueduan
Zhang, Shuangfei
Liang, Yili
author_facet Zhou, Jin
Zou, Kai
Fu, Shaodong
Duan, Zhenchun
Zhang, Guoqing
Wu, Xinhong
Huang, Jingwen
Li, Shihui
Liu, Xueduan
Zhang, Shuangfei
Liang, Yili
author_sort Zhou, Jin
collection PubMed
description Flavonoids are crucial in physiological and pharmaceutical processes, especially the treatment of cancer and the prevention of cardiovascular and cerebrovascular diseases. Flavonoid-producing plants and fungi have been extensively reported, but bacteria have been much less investigated as a source of flavonoid production. Deinococcus sp. 43, a spherical flavonoid-producing bacteria from the Ginkgo rhizosphere, was reported in this study. First, the whole genome of Deinococcus sp. 43 was sequenced and a series of flavonoid anabolic genes were annotated. Simultaneously, High Performance Liquid Chromatography (HPLC) results showed that Deinococcus sp. 43 was capable of producing flavonoids, with a maximum quercetin output of 2.9 mg/L. Moreover, the relative expression of key genes involved in flavonoid synthesis was determined to test the completeness of the flavonoid anabolic pathway. The results of LC-MS analysis demonstrated that the flavonoids produced by Deinococcus sp. 43 were significantly different between intracellular and extracellular environments. The concentration of multiple glycosylated flavonoids was substantially higher in extracellular than intracellular environments, while the majority of flavonoids obtained in intracellular environments were hydroxylated multiple times. Lastly, the flavonoid biosynthetic pathway of Deinococcus sp. 43 was constructed based on the genomic analysis and the detected flavonoids. In conclusion, this study represents the first comprehensive characterization of the flavonoid-producing pathway of Deinococcus. The findings demonstrate that the strain has excellent potential as a genetically engineered strain for the industrial production of flavonoids.
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spelling pubmed-103861652023-07-30 Flavonoid Synthesis by Deinococcus sp. 43 Isolated from the Ginkgo Rhizosphere Zhou, Jin Zou, Kai Fu, Shaodong Duan, Zhenchun Zhang, Guoqing Wu, Xinhong Huang, Jingwen Li, Shihui Liu, Xueduan Zhang, Shuangfei Liang, Yili Microorganisms Article Flavonoids are crucial in physiological and pharmaceutical processes, especially the treatment of cancer and the prevention of cardiovascular and cerebrovascular diseases. Flavonoid-producing plants and fungi have been extensively reported, but bacteria have been much less investigated as a source of flavonoid production. Deinococcus sp. 43, a spherical flavonoid-producing bacteria from the Ginkgo rhizosphere, was reported in this study. First, the whole genome of Deinococcus sp. 43 was sequenced and a series of flavonoid anabolic genes were annotated. Simultaneously, High Performance Liquid Chromatography (HPLC) results showed that Deinococcus sp. 43 was capable of producing flavonoids, with a maximum quercetin output of 2.9 mg/L. Moreover, the relative expression of key genes involved in flavonoid synthesis was determined to test the completeness of the flavonoid anabolic pathway. The results of LC-MS analysis demonstrated that the flavonoids produced by Deinococcus sp. 43 were significantly different between intracellular and extracellular environments. The concentration of multiple glycosylated flavonoids was substantially higher in extracellular than intracellular environments, while the majority of flavonoids obtained in intracellular environments were hydroxylated multiple times. Lastly, the flavonoid biosynthetic pathway of Deinococcus sp. 43 was constructed based on the genomic analysis and the detected flavonoids. In conclusion, this study represents the first comprehensive characterization of the flavonoid-producing pathway of Deinococcus. The findings demonstrate that the strain has excellent potential as a genetically engineered strain for the industrial production of flavonoids. MDPI 2023-07-21 /pmc/articles/PMC10386165/ /pubmed/37513020 http://dx.doi.org/10.3390/microorganisms11071848 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhou, Jin
Zou, Kai
Fu, Shaodong
Duan, Zhenchun
Zhang, Guoqing
Wu, Xinhong
Huang, Jingwen
Li, Shihui
Liu, Xueduan
Zhang, Shuangfei
Liang, Yili
Flavonoid Synthesis by Deinococcus sp. 43 Isolated from the Ginkgo Rhizosphere
title Flavonoid Synthesis by Deinococcus sp. 43 Isolated from the Ginkgo Rhizosphere
title_full Flavonoid Synthesis by Deinococcus sp. 43 Isolated from the Ginkgo Rhizosphere
title_fullStr Flavonoid Synthesis by Deinococcus sp. 43 Isolated from the Ginkgo Rhizosphere
title_full_unstemmed Flavonoid Synthesis by Deinococcus sp. 43 Isolated from the Ginkgo Rhizosphere
title_short Flavonoid Synthesis by Deinococcus sp. 43 Isolated from the Ginkgo Rhizosphere
title_sort flavonoid synthesis by deinococcus sp. 43 isolated from the ginkgo rhizosphere
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10386165/
https://www.ncbi.nlm.nih.gov/pubmed/37513020
http://dx.doi.org/10.3390/microorganisms11071848
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