Evidence map›Paper›PMID 26378232›Full record

ArticleThe Journal of biological chemistry2015

Identification of Middle Chain Fatty Acyl-CoA Ligase Responsible for the Biosynthesis of 2-Alkylmalonyl-CoAs for Polyketide Extender Unit.

Takeshi Miyazawa, Shunji Takahashi, Akihiro Kawata, Suresh Panthee, Teruo Hayashi, Takeshi Shimizu, Toshihiko Nogawa, Hiroyuki Osada

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 20 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Takeshi MiyazawaRIKEN Center for Sustainable Resource Science, Chemical Biology Research Group, Saitama 351-0198 and; the Graduate School of Science and Engineering, Saitama University, Saitama 338-8570, Japan.
Shunji TakahashiRIKEN Center for Sustainable Resource Science, Chemical Biology Research Group, Saitama 351-0198 and.
Akihiro Kawatathe Graduate School of Science and Engineering, Saitama University, Saitama 338-8570, Japan.
Suresh PantheeRIKEN Center for Sustainable Resource Science, Chemical Biology Research Group, Saitama 351-0198 and.
Teruo HayashiRIKEN Center for Sustainable Resource Science, Chemical Biology Research Group, Saitama 351-0198 and.
Takeshi ShimizuRIKEN Center for Sustainable Resource Science, Chemical Biology Research Group, Saitama 351-0198 and.
Toshihiko NogawaRIKEN Center for Sustainable Resource Science, Chemical Biology Research Group, Saitama 351-0198 and.
Hiroyuki OsadaRIKEN Center for Sustainable Resource Science, Chemical Biology Research Group, Saitama 351-0198 and; the Graduate School of Science and Engineering, Saitama University, Saitama 338-8570, Japan. Electronic address: shunjitaka@riken.jp.
RIKEN Center for Sustainable Resource Science · JPSaitama University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding the biosynthetic mechanism of the atypical polyketide extender unit is important for the development of bioactive natural products. Reveromycin (RM) derivatives produced by Streptomyces sp. SN-593 possess several aliphatic extender units. Here, we studied the molecular basis of 2-alkylmalonyl-CoA formation by analyzing the revR and revS genes, which form a transcriptional unit with the revT gene, a crotonyl-CoA carboxylase/reductase homolog. We mainly focused on the uncharacterized adenylate-forming enzyme (RevS). revS gene disruption resulted in the reduction of all RM derivatives, whereas reintroduction of the gene restored the yield of RMs. Although RevS was classified in the fatty acyl-AMP ligase clade based on phylogenetic analysis, biochemical characterization revealed that the enzyme catalyzed the middle chain fatty acyl-CoA ligase (FACL) but not the fatty acyl-AMP ligase activity, suggesting the molecular evolution for acyl-CoA biosynthesis. Moreover, we examined the in vitro conversion of fatty acid into 2-alkylmalonyl-CoA using purified RevS and RevT. The coupling reaction showed efficient conversion of hexenoic acid into butylmalonyl-CoA. RevS efficiently catalyzed C8-C10 middle chain FACL activity; therefore, we speculated that the acyl-CoA precursor was truncated via β-oxidation and converted into (E)-2-enoyl-CoA, a RevT substrate. To determine whether the β-oxidation process is involved between the RevS and RevT reaction, we performed the feeding experiment using [1,2,3,4-(13)C]octanoic acid. (13)C NMR analysis clearly demonstrated incorporation of the [3,4-(13)C]octanoic acid moiety into the structure of RM-A. Our results provide insight into the role of uncharacterized RevS homologs that may catalyze middle chain FACL to produce a unique polyketide extender unit.

Indexed as

Amino Acid SequenceBacterial ProteinsCoenzyme A LigasesGenes, BacterialMalonyl Coenzyme AMolecular Sequence DataMolecular StructurePhylogenyPolyketidesPyransRecombinant ProteinsSequence Homology, Amino AcidSpiro CompoundsStreptomycesSubstrate SpecificityBacterial ProteinsCoenzyme A LigasesMalonyl Coenzyme APolyketidesPyransRecombinant Proteinsreveromycin ASpiro Compoundsacyl-CoA ligasealkylmalonyl-CoAbiosynthesisenzyme catalysisnatural productpolyketidereveromycinsecondary metabolismStreptomyces

Identifiers

PMID26378232
PMCPMC4646404
OpenAlexW2149624053

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.