Evidence map›Paper›PMID 37217979›Full record

ArticleMicrobial cell factories2023

Involvement of a flavoprotein, acetohydroxyacid synthase, in growth and riboflavin production in riboflavin-overproducing Ashbya gossypii mutant.

Tatsuya Kato, Mai Kano, Ami Yokomori, Junya Azegami, Hesham A El Enshasy, Enoch Y Park

Open access · goldAbstract read
In one paragraph

Article in Microbial cell factories, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Review
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

6 authors at 2 institutions in 3 countries.

Tatsuya KatoMolecular and Biological Function Research Core, Research Institute of Green Science and Technology, Shizuoka University, Ohya 836, Suruga-Ku, Shizuoka, Japan. kato.tatsuya@shizuoka.ac.jp.
Mai KanoDepartment of Agriculture, Graduate School of Integrated Science and Technology, Shizuoka University, Ohya 836, Suruga-Ku, Shizuoka, Japan.
Ami YokomoriDepartment of Agriculture, Graduate School of Integrated Science and Technology, Shizuoka University, Ohya 836, Suruga-Ku, Shizuoka, Japan.
Junya AzegamiDepartment of Agriculture, Graduate School of Integrated Science and Technology, Shizuoka University, Ohya 836, Suruga-Ku, Shizuoka, Japan.
Hesham A El EnshasyInstitute of Bioproduct Development (IBD), Universiti Teknologi Malaysia (UTM), 81310 UTM, Johor Bahru, Malaysia.
Enoch Y ParkMolecular and Biological Function Research Core, Research Institute of Green Science and Technology, Shizuoka University, Ohya 836, Suruga-Ku, Shizuoka, Japan.
Shizuoka University · JPUniversity of Technology Malaysia · MY

Funding

Grant-in-Aid for Scientific Research (C) JP21K05390
6 · The paper itself

Abstract

backgroundPreviously, we isolated a riboflavin-overproducing Ashbya gossypii mutant (MT strain) and discovered some mutations in genes encoding flavoproteins. Here, we analyzed the riboflavin production in the MT strain, in view of flavoproteins, which are localized in the mitochondria.

resultsIn the MT strain, mitochondrial membrane potential was decreased compared with that in the wild type (WT) strain, resulting in increased reactive oxygen species. Additionally, diphenyleneiodonium (DPI), a universal flavoprotein inhibitor, inhibited riboflavin production in the WT and MT strains at 50 µM, indicating that some flavoproteins may be involved in riboflavin production. The specific activities of NADH and succinate dehydrogenases were significantly reduced in the MT strain, but those of glutathione reductase and acetohydroxyacid synthase were increased by 4.9- and 25-fold, respectively. By contrast, the expression of AgGLR1 gene encoding glutathione reductase was increased by 32-fold in the MT strain. However, that of AgILV2 gene encoding the catalytic subunit of acetohydroxyacid synthase was increased by only 2.1-fold. These results suggest that in the MT strain, acetohydroxyacid synthase, which catalyzes the first reaction of branched-chain amino acid biosynthesis, is vital for riboflavin production. The addition of valine, which is a feedback inhibitor of acetohydroxyacid synthase, to a minimal medium inhibited the growth of the MT strain and its riboflavin production. In addition, the addition of branched-chain amino acids enhanced the growth and riboflavin production in the MT strain.

conclusionThe significance of branched-chain amino acids for riboflavin production in A. gossypii is reported and this study opens a novel approach for the effective production of riboflavin in A. gossypii.

Indexed as

Acetolactate SynthaseEremotheciumFlavoproteinsMutationRiboflavinAmino Acids, Branched-ChainMitochondriaMitochondrial ProteinsReactive Oxygen SpeciesAcetolactate SynthaseAmino Acids, Branched-ChainFlavoproteinsMitochondrial ProteinsReactive Oxygen SpeciesRiboflavinAcetohydroxyacid synthaseAshbya gossypiiFlavoproteinRiboflavin

Identifiers

PMID37217979
PMCPMC10201721
OpenAlexW4377291770

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.