Evidence map›Paper›PMID 36658293›Full record

ArticleMolecular biotechnology2023

Engineering a Novel Metabolic Pathway for Improving Cellular Malonyl-CoA Levels in Escherichia coli.

Mohammad Hossein Moteallehi-Ardakani, Sedigheh Asad, Sayed-Amir Marashi, Afrooz Moghaddasi, Parisa Zarparvar

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Article in Molecular biotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 7 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

5 authors at 1 institution in 1 country.

Mohammad Hossein Moteallehi-ArdakaniDepartment of Biotechnology, College of Science, University of Tehran, Tehran, Iran.
Sedigheh AsadDepartment of Biotechnology, College of Science, University of Tehran, Tehran, Iran. asad@ut.ac.ir.ORCID http://orcid.org/0000-0003-0185-3817
Sayed-Amir MarashiDepartment of Biotechnology, College of Science, University of Tehran, Tehran, Iran.
Afrooz MoghaddasiDepartment of Biotechnology, College of Science, University of Tehran, Tehran, Iran.
Parisa ZarparvarDepartment of Biotechnology, College of Science, University of Tehran, Tehran, Iran.
University of Tehran · IR

Funding

Iran National Science Foundation 94017574
6 · The paper itself

Abstract

Cellular pool of malonyl-CoA in Escherichia coli is small, which impedes its utility for overproduction of natural products such as phenylpropanoids, polyketides, and flavonoids. In this study, we report the use of a new metabolic pathway to increase the malonyl-CoA concentration as a limiting metabolite in E. coli. For this purpose, the malonate/sodium symporter from Malonomonas rubra, and malonyl-CoA synthetase (MCS) from Bradyrhizobium japonicum were co-expressed in E. coli. This new pathway allows the cell to actively import malonate from the culture medium and to convert malonate and CoA to malonyl-CoA via an ATP-dependent ligation reaction. HPLC analysis confirmed elevated levels of malonyl-CoA and (2S)-naringenin as a malonyl-CoA-dependent metabolite, in E. coli. A 6.8-fold and more than 3.5-fold increase in (2S)-naringenin production were achieved in the engineered host in comparison with non-engineered E. coli and previously reported passive transport MatBMatC pathway, respectively. This observation suggests that using active transporters of malonate not only improves malonyl-CoA-dependent production but also makes it possible to harness low concentrations of malonate in culture media.

Indexed as

Escherichia coliMalonyl Coenzyme AFlavonoidsMalonatesMetabolic EngineeringMetabolic Networks and PathwaysFlavonoidsMalonatesMalonyl Coenzyme A(2S)-naringeninActive transportMalonyl-CoAMetabolic engineeringMicrobial chassis platform

Identifiers

PMID36658293
OpenAlexW4317494552

What OpenQuestion holds

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Registered trials

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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.