Evidence map›Paper›PMID 24406456›Full record

ArticleBioengineered

Whole cell biotransformation for reductive amination reactions.

Stephanie Klatte, Elisabeth Lorenz, Volker F Wendisch

Abstract readComment
In one paragraph

Article in Bioengineered. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Efficient synthesis of enantiopure amines from alcohols using restingGreen chemistry : an international journal and green chemistry resource : GC · 2019
    Article
  5. Article
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Stephanie KlatteChair of Genetics of Prokaryotes; Faculty of Biology & CeBiTec; Bielefeld University; Bielefeld, Germany.
Elisabeth LorenzChair of Genetics of Prokaryotes; Faculty of Biology & CeBiTec; Bielefeld University; Bielefeld, Germany.
Volker F WendischChair of Genetics of Prokaryotes; Faculty of Biology & CeBiTec; Bielefeld University; Bielefeld, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Whole cell biotransformation systems with enzyme cascading increasingly find application in biocatalysis to complement or replace established chemical synthetic routes for production of, e.g., fine chemicals. Recently, we established an Escherichia coli whole cell biotransformation system for reductive amination by coupling a transaminase and an amino acid dehydrogenase with glucose catabolism for cofactor recycling. Transformation of 2-keto-3-methylvalerate to l-isoleucine by E. coli cells was improved by genetic engineering of glucose metabolism for improved cofactor regeneration. Here, we compare this system with different strategies for cofactor regeneration such as cascading with alcohol dehydrogenases, with alternative production hosts such as Pseudomonas species or Corynebacterium glutamicum, and with improving whole cell biotransformation systems by metabolic engineering of NADPH regeneration.

Indexed as

Alanine DehydrogenaseBacillus subtilisEscherichia coliIsoleucineKeto AcidsTransaminasesAlanine DehydrogenaseIsoleucineKeto AcidsTransaminasesalanine dehydrogenasealcohol dehydrogenasecofactor recyclingCorynebacterium glutamicumE. coliformate dehydrogenaseglucose dehydrogenasePseudomonastransaminasewhole cell biotransformation

Identifiers

PMID24406456
PMCPMC4008469

What OpenQuestion holds

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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.