Evidence map›Paper›PMID 32103318›Full record

ArticleApplied microbiology and biotechnology2020

Development of a highly efficient and specific L-theanine synthase.

Jun Yao, Jing Li, Dandan Xiong, Yuanyuan Qiu, Guizhi Shi, Jian-Ming Jin, Yong Tao, Shuang-Yan Tang

Abstract read
PubMed Publisher
In one paragraph

Article in Applied microbiology and biotechnology, 2020. 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
1.3field-weighted citation impact, top 21% 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, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Pathway engineering ofMetabolic engineering communications · 2020
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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

8 authors at 5 institutions in 1 country.

Jun Yao *CAS Key Laboratory of Microbial Physiological and Metabolic Engineering, State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.
Jing Li *CAS Key Laboratory of Microbial Physiological and Metabolic Engineering, State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.
Dandan XiongCAS Key Laboratory of Microbial Physiological and Metabolic Engineering, State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.
Yuanyuan QiuCAS Key Laboratory of Microbial Physiological and Metabolic Engineering, State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.
Guizhi ShiUniversity of Chinese Academy of Sciences, Beijing, China.
Jian-Ming JinBeijing Key Laboratory of Plant Resources Research and Development, Beijing Technology and Business University, Beijing, China. jinjianming@btbu.edu.cn.
Yong TaoCAS Key Laboratory of Microbial Physiological and Metabolic Engineering, State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China. taoyong@im.ac.cn.
Shuang-Yan TangCAS Key Laboratory of Microbial Physiological and Metabolic Engineering, State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China. tangsy@im.ac.cn.
Microbiology Institute of Shaanxi · CNInstitute of Microbiology · CNBeijing Technology and Business University · CNChinese Academy of Sciences · CNUniversity of Chinese Academy of Sciences · CN

Funding

National Key Research and Development Program of China Grant 2018YFA0900701National Natural Science Foundation of China 31961133016National Natural Science Foundation of China 31971337National Natural Science Foundation of China 31971382
6 · The paper itself

Abstract

γ-Glutamylcysteine synthetase (γ-GCS) from Escherichia coli, which catalyzes the formation of L-glutamylcysteine from L-glutamic acid and L-cysteine, was engineered into an L-theanine synthase using L-glutamic acid and ethylamine as substrates. A high-throughput screening method using a 96-well plate was developed to evaluate the L-theanine synthesis reaction. Both site-saturation mutagenesis and random mutagenesis were applied. After three rounds of directed evolution, 13B6, the best-performing mutant enzyme, exhibited 14.6- and 17.0-fold improvements in L-theanine production and catalytic efficiency for ethylamine, respectively, compared with the wild-type enzyme. In addition, the specific activity of 13B6 for the original substrate, L-cysteine, decreased to approximately 14.6% of that of the wild-type enzyme. Thus, the γ-GCS enzyme was successfully switched to a specific L-theanine synthase by directed evolution. Furthermore, an ATP-regeneration system was introduced based on polyphosphate kinases catalyzing the transfer of phosphates from polyphosphate to ADP, thus lowering the level of ATP consumption and the cost of L-theanine synthesis. The final L-theanine production by mutant 13B6 reached 30.4 ± 0.3 g/L in 2 h, with a conversion rate of 87.1%, which has great potential for industrial applications.

Indexed as

Adenosine TriphosphateAmide SynthasesCatalysisDirected Molecular EvolutionEscherichia coliEthylaminesGlutamate-Cysteine LigaseGlutamatesGlutamic AcidHigh-Throughput Screening AssaysIndustrial MicrobiologyProtein EngineeringAdenosine TriphosphateAmide SynthasesethylamineEthylaminesGlutamate-Cysteine LigaseGlutamatesGlutamic AcidtheanineATP regenerationDirected evolutionHigh-throughput screeningL-Theanine synthaseγ-Glutamylcysteine synthetase (γ-GCS)

Identifiers

PMID32103318
OpenAlexW3008134699

What OpenQuestion holds

Textmetadata
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.