Evidence map›Paper›PMID 27796931›Full record

ArticleJournal of microbiology (Seoul, Korea)2016

A computationally simplistic poly-phasic approach to explore microbial communities from the Yucatan aquifer as a potential sources of novel natural products.

Miguel David Marfil-Santana, Aileen O'Connor-Sánchez, Jorge Humberto Ramírez-Prado, Cesar De Los Santos-Briones, Lluvia Korynthia López-Aguiar, Rafael Rojas-Herrera, Asunción Lago-Lestón, Alejandra Prieto-Davó

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In one paragraph

Article in Journal of microbiology (Seoul, Korea), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Miguel David Marfil-SantanaCenter for Scientific Investigation of Yucatan (CICY), Calle 43 No. 130, Colonia Chuburná de Hidalgo, Mérida, Yucatán, C.P. 97200, Mexico.
Aileen O'Connor-SánchezCenter for Scientific Investigation of Yucatan (CICY), Calle 43 No. 130, Colonia Chuburná de Hidalgo, Mérida, Yucatán, C.P. 97200, Mexico.
Jorge Humberto Ramírez-PradoCenter for Scientific Investigation of Yucatan (CICY), Calle 43 No. 130, Colonia Chuburná de Hidalgo, Mérida, Yucatán, C.P. 97200, Mexico.
Cesar De Los Santos-BrionesCenter for Scientific Investigation of Yucatan (CICY), Calle 43 No. 130, Colonia Chuburná de Hidalgo, Mérida, Yucatán, C.P. 97200, Mexico.
Lluvia Korynthia López-AguiarSchool of Chemistry, National Autonomous University of Mexico (UNAM), Campus Sisal, Puerto de Abrigo s/n Municipio de Hunucmá, Sisal, Yucatan, C.P. 97356, Mexico.
Rafael Rojas-HerreraSchool of Chemical Engeneering, Autonomous University of Yucatan (UADY), Periférico Norte Kilometro 33.5, Chuburná de Hidalgo Inn, Mérida, Yucatán, C.P. 97203, Mexico.
Asunción Lago-LestónPost Graduate Studies and Research Center of Ensenada (CICESE), Ensenada, Baja California, C.P. 22860, Mexico.
Alejandra Prieto-DavóSchool of Chemistry, National Autonomous University of Mexico (UNAM), Campus Sisal, Puerto de Abrigo s/n Municipio de Hunucmá, Sisal, Yucatan, C.P. 97356, Mexico. apdavo@unam.mx.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The need for new antibiotics has sparked a search for the microbes that might potentially produce them. Current sequencing technologies allow us to explore the biotechnological potential of microbial communities in diverse environments without the need for cultivation, benefitting natural product discovery in diverse ways. A relatively recent method to search for the possible production of novel compounds includes studying the diverse genes belonging to polyketide synthase pathways (PKS), as these complex enzymes are an important source of novel therapeutics. In order to explore the biotechnological potential of the microbial community from the largest underground aquifer in the world located in the Yucatan, we used a polyphasic approach in which a simple, non-computationally intensive method was coupled with direct amplification of environmental DNA to assess the diversity and novelty of PKS type I ketosynthase (KS) domains. Our results suggest that the bioinformatic method proposed can indeed be used to assess the novelty of KS enzymes; nevertheless, this in silico study did not identify some of the KS diversity due to primer bias and stringency criteria outlined by the metagenomics pipeline. Therefore, additionally implementing a method involving the direct cloning of KS domains enhanced our results. Compared to other freshwater environments, the aquifer was characterized by considerably less diversity in relation to known ketosynthase domains; however, the metagenome included a family of KS type I domains phylogenetically related, but not identical, to those found in the curamycin pathway, as well as an outstanding number of thiolases. Over all, this first look into the microbial community found in this large Yucatan aquifer and other fresh water free living microbial communities highlights the potential of these previously overlooked environments as a source of novel natural products.

Indexed as

GroundwaterMetagenomicsBiological ProductsComputational BiologyDrug DiscoveryFresh WaterGenetic VariationMetagenomeMicrobial ConsortiaPhylogenyPolyketide SynthasesSecondary MetabolismBiological ProductsPolyketide Synthasesmicrobial metagenomicsnatural product discoverypolyketide synthasesecondary metabolitesYucatan aquifer

Identifiers

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Registered trials

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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.