2021
DOI: 10.1016/j.funbio.2020.10.010
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Functional analysis of a chaetoglobosin A biosynthetic regulator in Chaetomium globosum

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Cited by 12 publications
(20 citation statements)
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“…4 ), indicated that CgVeA played an important regulatory role in the biosynthesis of cheA by controlling the transcription levels of the core enzymes in the gene cluster. Furthermore, the results showed that effectively enhanced expression of CgVeA had a positive impact on the expression levels of LaeA and cheR , which were identified to be positively correlated with cheA biosynthesis [ 13 ], especially under light condition. In contrast, both LaeA and cheR were obviously reduced in PS ( Fig.…”
Section: Resultsmentioning
confidence: 99%
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“…4 ), indicated that CgVeA played an important regulatory role in the biosynthesis of cheA by controlling the transcription levels of the core enzymes in the gene cluster. Furthermore, the results showed that effectively enhanced expression of CgVeA had a positive impact on the expression levels of LaeA and cheR , which were identified to be positively correlated with cheA biosynthesis [ 13 ], especially under light condition. In contrast, both LaeA and cheR were obviously reduced in PS ( Fig.…”
Section: Resultsmentioning
confidence: 99%
“…In the past 5 years, our research group has progressively explored the factors influencing cheA production. CgLaeA and CgcheR, the Zn(II) 2 Cys 6 structural and pathway-specific transcription factors, respectively, have been identified in C. globosum , and have been found to exert positive effects (especially, CgcheR ) on target compounds synthesis [ 13 , 33 ]. Furthermore, EMSA results have revealed that CgcheR shared a relatively strong shift signal to PKS gene, which has been reported to be associated with polymerization of monomeric substance to form the carbon backbone [ 12 ].…”
Section: Discussionmentioning
confidence: 99%
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“…After a spontaneous intramolecular condensation and a Diels-Alder reaction, the key intermediate prochaetoglobosin is generated, which can be furnished into ChA after a set of oxidative modifications. Through gene disruption, homologs of CheA (CgcheA with a gene locus CHGG_01239) and CheB (CgcheB with a gene locus CHGG_01238) as well as the enzymes CheD (CgcheE with a gene locus CHGG_01242-1), CheE (CgcheF with a gene locus CHGG_01242-2), and CheG (CgcheG with a gene locus CHGG_01243), involved in the final oxidative transformations, are identified and characterized in C. globosum [17,18]. Nonetheless, we previously observed in C. globosum NK102 that a putative pigment polyketide synthase gene, pks-1/alb1, was also required for ChA biosynthesis [19].…”
Section: Introductionmentioning
confidence: 99%