Evidence map›Paper›PMID 26753612›Full record

ArticleScientific reports2016

Mechanism of 2,3-butanediol stereoisomers formation in a newly isolated Serratia sp. T241.

Liaoyuan Zhang, Zewang Guo, Jiebo Chen, Quanming Xu, Hui Lin, Kaihui Hu, Xiong Guan, Yaling Shen

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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Microbial 2-butanol production withBiotechnology for biofuels · 2019
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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.

Liaoyuan ZhangKey Laboratory of Biopesticide and Chemical Biology, Ministry of Education, College of Life Science, Fujian Agriculture and Forestry University, FuZhou, Fujian province, 350002, PR China.
Zewang GuoKey Laboratory of Biopesticide and Chemical Biology, Ministry of Education, College of Life Science, Fujian Agriculture and Forestry University, FuZhou, Fujian province, 350002, PR China.
Jiebo ChenKey Laboratory of Biopesticide and Chemical Biology, Ministry of Education, College of Life Science, Fujian Agriculture and Forestry University, FuZhou, Fujian province, 350002, PR China.
Quanming XuKey Laboratory of Biopesticide and Chemical Biology, Ministry of Education, College of Life Science, Fujian Agriculture and Forestry University, FuZhou, Fujian province, 350002, PR China.
Hui LinKey Laboratory of Biopesticide and Chemical Biology, Ministry of Education, College of Life Science, Fujian Agriculture and Forestry University, FuZhou, Fujian province, 350002, PR China.
Kaihui HuKey Laboratory of Biopesticide and Chemical Biology, Ministry of Education, College of Life Science, Fujian Agriculture and Forestry University, FuZhou, Fujian province, 350002, PR China.
Xiong GuanKey Laboratory of Biopesticide and Chemical Biology, Ministry of Education, College of Life Science, Fujian Agriculture and Forestry University, FuZhou, Fujian province, 350002, PR China.
Yaling ShenState Key Laboratory of Bioreactor Engineering, New World Institute of Biotechnology, East China University of Science and Technology, Shanghai, 200237, PR China.
Fujian Agriculture and Forestry University · CNEast China University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Serratia sp. T241, a newly isolated xylose-utilizing strain, produced three 2,3-butanediol (2,3-BD) stereoisomers. In this study, three 2,3-butanediol dehydrogenases (BDH1-3) and one glycerol dehydrogenase (GDH) involved in 2,3-BD isomers formation by Serratia sp. T241 were identified. In vitro conversion showed BDH1 and BDH2 could catalyzed (3S)-acetoin and (3R)-acetoin into (2S,3S)-2,3-BD and meso-2,3-BD, while BDH3 and GDH exhibited the activities from (3S)-acetoin and (3R)-acetoin to meso-2,3-BD and (2R,3R)-2,3-BD. Four encoding genes were assembled into E. coli with budA (acetolactate decarboxylase) and budB (acetolactate synthase), responsible for converting pyruvate into acetoin. E. coli expressing budAB-bdh1/2 produced meso-2,3-BD and (2S,3S)-2,3-BD. Correspondingly, (2R,3R)-2,3-BD and meso-2,3-BD were obtained by E. coli expressing budAB-bdh3/gdh. These results suggested four enzymes might contribute to 2,3-BD isomers formation. Mutants of four genes were developed in Serratia sp. T241. Δbdh1 led to reduced concentration of meso-2,3-BD and (2S,3S)-2,3-BD by 97.7% and 87.9%. (2R,3R)-2,3-BD with a loss of 73.3% was produced by Δbdh3. Enzyme activity assays showed the decrease of 98.4% and 22.4% by Δbdh1 and Δbdh3 compared with the wild strain. It suggested BDH1 and BDH3 played important roles in 2,3-BD formation, BDH2 and GDH have small effects on 2,3-BD production by Serratia sp. T241.

Indexed as

Butylene GlycolsCatalysisEnzyme ActivationEscherichia coliFermentationGene OrderHydroxybutyrate DehydrogenaseKineticsOperonPlasmidsSequence DeletionSerratiaStereoisomerismSugar Alcohol Dehydrogenases2,3-butylene glycolButylene Glycolsgalactitol 2-dehydrogenaseHydroxybutyrate DehydrogenaseSugar Alcohol Dehydrogenases

Identifiers

PMID26753612
PMCPMC4709696
OpenAlexW2404844590

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.