Screening of polyketide genes from Brazilian Atlantic Forest soil / Evaluación de genes biosintéticos de policétidos provenientes de suelo de la selva atlántica brasileñae / Avaliação de genes biossintéticos de policetídeos provenientes do solo da Mata Atlântica Brasileira

Abstract Soil is a large source of microorganisms with potential to produce bioactive compounds. Since most of them cannot be cultured, metagenomics has become a useful tool in order to evaluate this potential. The aim of this study was to screen biosynthetic polyketide genes (PKS) present in a metagenomic library constructed from a soil sample isolated from the Brazilian Atlantic Forest. The library comprises 5000 clones with DNA inserts between 40 and 50 Kb. The characterization of the biosynthetic gene clusters of these molecules is a promising alternative to elucidate the biotechnological potential of bioactive compounds in microbial communities. The PKS genes were screened using degenerated primers. The positive clones for PKS systems were isolated, and their nucleotide sequences analysed with bioinformatics tools. The screening yielded two positive clones for PKS II genes. Furthermore, variations in the sequences of the PKS II genes from the metagenomic library were observed when compared with sequences of ketosynthases' databases. With these findings we gain insight into the possible relation between new biosynthetic genes and the production of new secondary metabolites.

Resumen El suelo es una fuente importante de microrganismos con potencial para producir compuestos bioactivos. Dado que la gran mayoría de estos microorganismos no puede cultivarse, la metagenómica se ha convertido en una herramienta útil para evaluar dicho potencial. El objetivo del presente estudio fue evaluar los genes biosintéticos de policétidos (PKS) presentes en una biblioteca metagenómica construida a partir de una muestra de suelo aislada de la selva atlántica brasileña. La biblioteca comprende 5000 clones con insertos de DNA entre 40 y 50 Kb. La caracterización de clústeres de genes biosintéticos de estas moléculas es una alternativa promisoria para elucidar el potencial biotecnológico de los compuestos bioactivos en comunidades microbianas. Los genes biosintéticos de PKS se evaluaron usando cebadores degenerados. Se aislaron los clones positivos para sistemas PKS y sus secuencias de nucleótidos se analizaron con herramientas bioinformáticas. La evaluación arrojó dos clones positivos para genes de PKS II. Además, se observaron variaciones en las secuencias de genes de PKS II de la biblioteca metagenómica cuando se compararon con las secuencias de las bases de datos de cetosintasas. Estos hallazgos proporcionan nueva información sobre la posible relación entre nuevos genes biosintéticos y la producción de nuevos metabolitos secundarios.

Resumo O solo é uma fonte de importante de microrganismos com potencial para produzir compostos bioativos. Considerando que a maioria destes microrganismos não se pode cultivar, a metagenômica tem se convertido em uma ferramenta útil para avaliar este potencial. O objetivo deste estudo foi avaliar os genes biossintéticos de policetídeos (PKS) presentes em uma biblioteca metagenômica construída a partir de uma amostra de solo isolada da Mata Atlântica brasileira. A biblioteca compreende 5000 clones com insertos de DNA entre 40 e 50 Kb. A caracterização de clusters de genes biossintéticos destas moléculas é uma alternativa promissora para elucidar o potencial biotecnológico de compostos bioativos em comunidades microbianas. Os genes PKS foram avaliados usando primers degenerados. Os clones positivos para sistemas PKS foram isolados e suas sequências de nucleotídeos foram analisadas com ferramentas de bioinformática. A avaliação forneceu dois clones positivos para genes PKS II. Além disso, variações nas sequências dos genes PKS II da biblioteca metagenômica foram observadas quando comparadas com sequências da base de dados de cetosintases. Com estas descobertas obtivemos uma visão sobre uma possível relação entre novos genes biossintéticos e a produção de novos metabólitos secundários.

Bioprospección de la actividad antimicrobiana de los extractos de los hongos endófitos de Bauhinia guianensis / Bioprospecting of antimicrobial activity of extracts of endophytic fungi from Bauhinia guianensis

Antibiotic resistance results in higher medical costs, prolonged hospital stays and increased mortality and is rising to dangerously high levels in all parts of the world. Therefore, this study aims to search for new antimicrobial agents through bioprospecting of extracts of endophytic fungi from Bauhinia guianensis, a typical Amazonian plant used in combating infections. Seventeen (17) fungi were isolated and as result the methanolic extract of the fungus Exserohilum rostratum showed good activity against the bacteria tested. The polyketide monocerin was isolated by the chromatographic technique, identified by NMR and MS, showing broad antimicrobial spectrum.

La resistencia a los antibióticos conduce a mayores costos médicos, hospitalizaciones prolongadas e incremento de la mortalidad, y está aumentando a niveles peligrosamente altos en todas partes del mundo. Este estudio tuvo como objetivo la búsqueda de nuevos agentes antimicrobianos a través de la bioprospección de extractos de hongos endófitos de Bauhinia guianensis, una planta amazónica típica, utilizada en la lucha contra problemas infecciosos. Fueron aislados 17 hongos; el extracto metanólico del hongo Exserohilum rostratum mostró buena actividad contra las bacterias probadas. Se aisló monocerina policétido por la técnica de cromatografía; este compuesto fue identificado por RM y EM, y mostró un amplio espectro antimicrobiano.

Biotechnology of polyketides: new breath of life for the novel antibiotic genetic pathways discovery through metagenomics

The discovery of secondary metabolites produced by microorganisms (e.g., penicillin in 1928) and the beginning of their industrial application (1940) opened new doors to what has been the main medication source for the treatment of infectious diseases and tumors. In fact, approximately 80 years after the discovery of the first antibiotic compound, and despite all of the warnings about the failure of the "goose that laid the golden egg," the potential of this wealth is still inexorable: simply adjust the focus from "micro" to "nano", that means changing the look from microorganisms to nanograms of DNA. Then, the search for new drugs, driven by genetic engineering combined with metagenomic strategies, shows us a way to bypass the barriers imposed by methodologies limited to isolation and culturing. However, we are far from solving the problem of supplying new molecules that are effective against the plasticity of multi- or pan-drug-resistant pathogens. Although the first advances in genetic engineering date back to 1990, there is still a lack of high-throughput methods to speed up the screening of new genes and design new molecules by recombination of pathways. In addition, it is necessary an increase in the variety of heterologous hosts and improvements throughout the full drug discovery pipeline. Among numerous studies focused on this subject, those on polyketide antibiotics stand out for the large technical-scientific efforts that established novel solutions for the transfer/engineering of major metabolic pathways using transposons and other episomes, overcoming one of the main methodological constraints for the heterologous expression of major pathways. In silico prediction analysis of three-dimensional enzymatic structures and advances in sequencing technologies have expanded access to the metabolic potential of microorganisms.