Evidence map›Paper›PMID 27586788›Full record

ArticleScientific reports2016

Enhanced pinocembrin production in Escherichia coli by regulating cinnamic acid metabolism.

Weijia Cao, Weichao Ma, Xin Wang, Bowen Zhang, Xun Cao, Kequan Chen, Yan Li, Pingkai Ouyang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Optimization of Pinocembrin Biosynthesis inACS synthetic biology · 2023
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. EngineeringSynthetic biology (Oxford, England) · 2020
    Article
  9. Review
  10. Article
  11. Article
  12. Article
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.

Weijia CaoState Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing 211816, P.R. China.
Weichao MaState Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing 211816, P.R. China.
Xin WangState Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing 211816, P.R. China.
Bowen ZhangState Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing 211816, P.R. China.
Xun CaoState Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing 211816, P.R. China.
Kequan ChenState Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing 211816, P.R. China.
Yan LiState Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing 211816, P.R. China.
Pingkai OuyangState Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing 211816, P.R. China.
Nanjing Tech University · CNState Key Laboratory of Materials-Oriented Chemical Engineering

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microbial biosynthesis of pinocembrin is of great interest in the area of drug research and human healthcare. Here we found that the accumulation of the pathway intermediate cinnamic acid adversely affected pinocembrin production. Hence, a stepwise metabolic engineering strategy was carried out aimed at eliminating this pathway bottleneck and increasing pinocembrin production. The screening of gene source and the optimization of gene expression was first employed to regulate the synthetic pathway of cinnamic acid, which showed a 3.53-fold increase in pinocembrin production (7.76 mg/L) occurred with the alleviation of cinnamic acid accumulation in the engineered E. coli. Then, the downstream pathway that consuming cinnamic acid was optimized by the site-directed mutagenesis of chalcone synthase and cofactor engineering. S165M mutant of chalcone synthase could efficiently improve the pinocembrin production, and allowed the product titer of pinocembrin increased to 40.05 mg/L coupled with the malonyl-CoA engineering. With a two-phase pH fermentation strategy, the cultivation of the optimized strain resulted in a final pinocembrin titer of 67.81 mg/L. The results and engineering strategies demonstrated here would hold promise for the titer improvement of other flavonoids.

Indexed as

AcyltransferasesBatch Cell Culture TechniquesBiomassCinnamatesEscherichia coliFermentationFlavanonesGene DosageGene ExpressionGlucoseHydrogen-Ion ConcentrationMalonyl Coenzyme AMetabolic EngineeringMutagenesis, Site-DirectedPhenylalaninePlasmidsAcyltransferasesCinnamatescinnamic acidFlavanonesflavanone synthetaseGlucoseMalonyl Coenzyme APhenylalaninepinocembrin

Identifiers

PMID27586788
PMCPMC5009306
OpenAlexW2508854755

What OpenQuestion holds

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LicenceCC BY
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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.