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Article: Functional Characterization of Long-Chain Acyl-CoA Synthetase Gene Family from the Oleaginous Alga Chromochloris zofingiensis

TitleFunctional Characterization of Long-Chain Acyl-CoA Synthetase Gene Family from the Oleaginous Alga Chromochloris zofingiensis
Authors
KeywordsChromochloris zofingiensis
functional characterization
long-chain acyl-CoA synthetase
trait improvement
transcription factor
triacylglycerol
Issue Date2020
Citation
Journal of Agricultural and Food Chemistry, 2020, v. 68, n. 15, p. 4473-4484 How to Cite?
AbstractLong-chain acyl-coenzyme A (CoA) synthetase (LACS) catalyzes the formation of acyl-CoAs from free fatty acids, which is pivotal for lipid metabolism. Here, we confirmed the presence of six CzLACS genes in Chromochloris zofingiensis. Functional complementation and in vitro enzymatic assay indicated that CzLACS2 through CzLACS5 rather than CzLACS1 or CzLACS6 are bona fide LACS enzymes and they have overlapping yet distinct substrate preference. The results of the subcellular colocalization experiment and different expression patterns under three triacylglycerol (TAG)-inducing conditions showed that CzLACS2 through CzLACS4 reside at endoplasmic reticulum (ER) and are involved in TAG biosynthesis, while CzLACS5 resides in peroxisome and participates in fatty acid β-oxidation. The yeast one-hybrid assay using a library of 50 transcription factors (TFs) constructed in our study identified 12 TFs potentially involved in regulating the expression of CzLACSs. Moreover, heterologous expression of CzLACSs demonstrated their engineering potential for modulating TAG synthesis in yeast and algal cells.
Persistent Identifierhttp://hdl.handle.net/10722/329621
ISSN
2021 Impact Factor: 5.895
2020 SCImago Journal Rankings: 1.203

 

DC FieldValueLanguage
dc.contributor.authorWu, Tao-
dc.contributor.authorFu, Yunlei-
dc.contributor.authorShi, Ying-
dc.contributor.authorLi, Yuelian-
dc.contributor.authorKou, Yaping-
dc.contributor.authorMao, Xuemei-
dc.contributor.authorLiu, Jin-
dc.date.accessioned2023-08-09T03:34:06Z-
dc.date.available2023-08-09T03:34:06Z-
dc.date.issued2020-
dc.identifier.citationJournal of Agricultural and Food Chemistry, 2020, v. 68, n. 15, p. 4473-4484-
dc.identifier.issn0021-8561-
dc.identifier.urihttp://hdl.handle.net/10722/329621-
dc.description.abstractLong-chain acyl-coenzyme A (CoA) synthetase (LACS) catalyzes the formation of acyl-CoAs from free fatty acids, which is pivotal for lipid metabolism. Here, we confirmed the presence of six CzLACS genes in Chromochloris zofingiensis. Functional complementation and in vitro enzymatic assay indicated that CzLACS2 through CzLACS5 rather than CzLACS1 or CzLACS6 are bona fide LACS enzymes and they have overlapping yet distinct substrate preference. The results of the subcellular colocalization experiment and different expression patterns under three triacylglycerol (TAG)-inducing conditions showed that CzLACS2 through CzLACS4 reside at endoplasmic reticulum (ER) and are involved in TAG biosynthesis, while CzLACS5 resides in peroxisome and participates in fatty acid β-oxidation. The yeast one-hybrid assay using a library of 50 transcription factors (TFs) constructed in our study identified 12 TFs potentially involved in regulating the expression of CzLACSs. Moreover, heterologous expression of CzLACSs demonstrated their engineering potential for modulating TAG synthesis in yeast and algal cells.-
dc.languageeng-
dc.relation.ispartofJournal of Agricultural and Food Chemistry-
dc.subjectChromochloris zofingiensis-
dc.subjectfunctional characterization-
dc.subjectlong-chain acyl-CoA synthetase-
dc.subjecttrait improvement-
dc.subjecttranscription factor-
dc.subjecttriacylglycerol-
dc.titleFunctional Characterization of Long-Chain Acyl-CoA Synthetase Gene Family from the Oleaginous Alga Chromochloris zofingiensis-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/acs.jafc.0c01284-
dc.identifier.pmid32208653-
dc.identifier.scopuseid_2-s2.0-85084392160-
dc.identifier.volume68-
dc.identifier.issue15-
dc.identifier.spage4473-
dc.identifier.epage4484-
dc.identifier.eissn1520-5118-

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