Literature DB >> 21732240

Metabolic engineering of flavonoids in plants and microorganisms.

Yechun Wang1, Steven Chen, Oliver Yu.   

Abstract

Over 9,000 flavonoid compounds have been found in various plants, comprising one of the largest families of natural products. Flavonoids are an essential factor in plant interactions with the environment, often serving as the first line of defense against UV irradiation and pathogen attacks. Flavonoids are also major nutritional compounds in foods and beverages, with demonstrated health benefits. Some flavonoids are potent antioxidants, and specific flavonoid compounds are beneficial in many physiological and pharmacological processes. Therefore, engineering of flavonoid biosynthesis in plants or in microorganisms has significant scientific and economical importance. Construction of biosynthetic pathways in heterologous systems offers promising results for large-scale flavonoid production by fermentation or bioconversion. Genomics and metabolomics now offer unprecedented tools for detailed understanding of the engineered transgenic organism and for developing novel technologies to further increase flavonoid production yields. We summarize some of the recent metabolic engineering strategies in plants and microorganisms, with a focus on applications of metabolic flux analysis. We are confident that these engineering approaches will lead to successful industrial flavonoid production in the near future.

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Year:  2011        PMID: 21732240     DOI: 10.1007/s00253-011-3449-2

Source DB:  PubMed          Journal:  Appl Microbiol Biotechnol        ISSN: 0175-7598            Impact factor:   4.813


  59 in total

Review 1.  The re-emergence of natural products for drug discovery in the genomics era.

Authors:  Alan L Harvey; RuAngelie Edrada-Ebel; Ronald J Quinn
Journal:  Nat Rev Drug Discov       Date:  2015-01-23       Impact factor: 84.694

2.  Asymmetric Methods for the Synthesis of Flavanones, Chromanones, and Azaflavanones.

Authors:  Antoinette E Nibbs; Karl A Scheidt
Journal:  European J Org Chem       Date:  2011-12-09

3.  Pyramiding of tea Dihydroflavonol reductase and Anthocyanidin reductase increases flavan-3-ols and improves protective ability under stress conditions in tobacco.

Authors:  Vinay Kumar; Sudesh Kumar Yadav
Journal:  3 Biotech       Date:  2017-06-29       Impact factor: 2.406

4.  Efficient synthesis of eriodictyol from L-tyrosine in Escherichia coli.

Authors:  Saijie Zhu; Junjun Wu; Guocheng Du; Jingwen Zhou; Jian Chen
Journal:  Appl Environ Microbiol       Date:  2014-03-07       Impact factor: 4.792

5.  Development of an autonomous and bifunctional quorum-sensing circuit for metabolic flux control in engineered Escherichia coli.

Authors:  Christina V Dinh; Kristala L J Prather
Journal:  Proc Natl Acad Sci U S A       Date:  2019-12-03       Impact factor: 11.205

6.  Putting bugs to the blush: metabolic engineering for phenylpropanoid-derived products in microorganisms.

Authors:  Philana V van Summeren-Wesenhagen; Jan Marienhagen
Journal:  Bioengineered       Date:  2013-11-18       Impact factor: 3.269

7.  The disruption of the MAPKK gene triggering the synthesis of flavonoids in endophytic fungus Phomopsis liquidambaris.

Authors:  Qian Yang; Mei Wu; Ya-Li Zhu; Ya-Qiong Yang; Yan-Zhen Mei; Chuan-Chao Dai
Journal:  Biotechnol Lett       Date:  2020-10-31       Impact factor: 2.461

8.  Improved pinocembrin production in Escherichia coli by engineering fatty acid synthesis.

Authors:  Weijia Cao; Weichao Ma; Bowen Zhang; Xin Wang; Kequan Chen; Yan Li; Pingkai Ouyang
Journal:  J Ind Microbiol Biotechnol       Date:  2016-01-05       Impact factor: 3.346

Review 9.  The role of flavonoids in the establishment of plant roots endosymbioses with arbuscular mycorrhiza fungi, rhizobia and Frankia bacteria.

Authors:  Khalid Abdel-Lateif; Didier Bogusz; Valérie Hocher
Journal:  Plant Signal Behav       Date:  2012-05-14

10.  The roles of a flavone-6-hydroxylase and 7-O-demethylation in the flavone biosynthetic network of sweet basil.

Authors:  Anna Berim; David R Gang
Journal:  J Biol Chem       Date:  2012-11-26       Impact factor: 5.157

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