Evidence map›Paper›PMID 27610105›Full record

ArticleFrontiers in microbiology2016

Sequence-Based Screening for Rare Enzymes: New Insights into the World of AMDases Reveal a Conserved Motif and 58 Novel Enzymes Clustering in Eight Distinct Families.

Janine Maimanakos, Jennifer Chow, Sarah K Gaßmeyer, Simon Güllert, Florian Busch, Robert Kourist, Wolfgang R Streit

Open access · goldAbstract read
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Article in Frontiers in microbiology, 2016. 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
1.0field-weighted citation impact, top 22% 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

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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, 15 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Janine MaimanakosDepartment of Microbiology and Biotechnology, Biocenter Klein Flottbek, University of Hamburg Hamburg, Germany.
Jennifer ChowDepartment of Microbiology and Biotechnology, Biocenter Klein Flottbek, University of Hamburg Hamburg, Germany.
Sarah K GaßmeyerJunior Research Group for Microbial Biotechnology, Ruhr-University Bochum Bochum, Germany.
Simon GüllertDepartment of Microbiology and Biotechnology, Biocenter Klein Flottbek, University of Hamburg Hamburg, Germany.
Florian BuschJunior Research Group for Microbial Biotechnology, Ruhr-University Bochum Bochum, Germany.
Robert KouristJunior Research Group for Microbial Biotechnology, Ruhr-University Bochum Bochum, Germany.
Wolfgang R StreitDepartment of Microbiology and Biotechnology, Biocenter Klein Flottbek, University of Hamburg Hamburg, Germany.
Universität Hamburg · DERuhr University Bochum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Arylmalonate Decarboxylases (AMDases, EC 4.1.1.76) are very rare and mostly underexplored enzymes. Currently only four known and biochemically characterized representatives exist. However, their ability to decarboxylate α-disubstituted malonic acid derivatives to optically pure products without cofactors makes them attractive and promising candidates for the use as biocatalysts in industrial processes. Until now, AMDases could not be separated from other members of the aspartate/glutamate racemase superfamily based on their gene sequences. Within this work, a search algorithm was developed that enables a reliable prediction of AMDase activity for potential candidates. Based on specific sequence patterns and screening methods 58 novel AMDase candidate genes could be identified in this work. Thereby, AMDases with the conserved sequence pattern of Bordetella bronchiseptica's prototype appeared to be limited to the classes of Alpha-, Beta-, and Gamma-proteobacteria. Amino acid homologies and comparison of gene surrounding sequences enabled the classification of eight enzyme clusters. Particularly striking is the accumulation of genes coding for different transporters of the tripartite tricarboxylate transporters family, TRAP transporters and ABC transporters as well as genes coding for mandelate racemases/muconate lactonizing enzymes that might be involved in substrate uptake or degradation of AMDase products. Further, three novel AMDases were characterized which showed a high enantiomeric excess (>99%) of the (R)-enantiomer of flurbiprofen. These are the recombinant AmdA and AmdV from Variovorax sp. strains HH01 and HH02, originated from soil, and AmdP from Polymorphum gilvum found by a data base search. Altogether our findings give new insights into the class of AMDases and reveal many previously unknown enzyme candidates with high potential for bioindustrial processes.

Indexed as

arylmalonate decarboxylase (AMDase)decarboxylationflurbiprofenHidden Markov ModelsPolymorphum gilvumracemasesequence-based screeningVariovorax sp.

Identifiers

PMID27610105
PMCPMC4996985
OpenAlexW2513873200

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