Evidence map›Paper›PMID 27369765›Full record

ArticleJournal of industrial microbiology & biotechnology2016

Evolving the L-lysine high-producing strain of Escherichia coli using a newly developed high-throughput screening method.

Yan Wang, Qinggang Li, Ping Zheng, Yanmei Guo, Lixian Wang, Tongcun Zhang, Jibin Sun, Yanhe Ma

Abstract read
In one paragraph

Article in Journal of industrial microbiology & biotechnology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. OptimizingFrontiers in microbiology · 2024
    Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. High-yield production of L-serine from glycerol by engineered Escherichia coli.Journal of industrial microbiology & biotechnology · 2019
    Article
  14. Deep scanning lysine metabolism inMolecular systems biology · 2018
    Article
  15. In vivo biosensors: mechanisms, development, and applications.Journal of industrial microbiology & biotechnology · 2018
    Article
  16. 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.

Yan WangCollege of Biotechnology, Tianjin University of Science and Technology, Tianjin, People's Republic of China.
Qinggang LiKey Laboratory of Systems Microbial Biotechnology, Chinese Academy of Sciences, Tianjin, People's Republic of China.
Ping ZhengKey Laboratory of Systems Microbial Biotechnology, Chinese Academy of Sciences, Tianjin, People's Republic of China. zheng_p@tib.cas.cn.
Yanmei GuoTianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, People's Republic of China.
Lixian WangTianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, People's Republic of China.
Tongcun ZhangCollege of Biotechnology, Tianjin University of Science and Technology, Tianjin, People's Republic of China.
Jibin SunKey Laboratory of Systems Microbial Biotechnology, Chinese Academy of Sciences, Tianjin, People's Republic of China. sun_jb@tib.cas.cn.
Yanhe MaTianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, People's Republic of China.

Funding

NIAAA NIH HHS L40 AA023402
6 · The paper itself

Abstract

This study provided a new method which applied a selected L-lysine-inducible promoter for evolving lysine industrial strains of E. coli. According to the intracellular levels of the enhanced green fluorescent protein (EGFP) whose expression was controlled by the promoter, 186 strains were preliminarily selected using fluorescence-activated cell sorting from a 10-million-mutant library generated from a L-lysine high-producing E. coli strain. By subsequent multiple parameter evaluation of the 186 selected strains according to the concentration and the yield of lysine, the productivity per unit of cell in 96-deep-well blocks, two mutants MU-1 and MU-2 were obtained. They produced 136.51 ± 1.55 and 133.2 9 ± 1.42 g/L of lysine, respectively, in 5-L jars. Compared with the lysine concentration and the yield of the original strain, those of strain MU-1 improved by 21.00 and 9.05 %, respectively, and those of strain MU-2 improved by 18.14 and 10.41 %, respectively. The mutant selection and evaluation system newly established in our study should be useful for continuous improvement of the current E. coli strains in the lysine industry.

Indexed as

Biosensing TechniquesCell SeparationDirected Molecular EvolutionEscherichia coliFlow CytometryGene LibraryGreen Fluorescent ProteinsHigh-Throughput Screening AssaysIndustrial MicrobiologyLysinePromoter Regions, Geneticenhanced green fluorescent proteinGreen Fluorescent ProteinsLysineEscherichia coliHigh-throughput screeningLysine biosensorLysine productionStrain evolution

Identifiers

PMID27369765
PMCPMC4983297

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.