Analysis and gene expression of PKS II and carbohydrases from metagenomic libraries
| Grant number: | 11/12025-2 |
| Support type: | Scholarships in Brazil - Scientific Initiation |
| Effective date (Start): | September 01, 2011 |
| Effective date (End): | December 31, 2012 |
| Field of knowledge: | Biological Sciences - Microbiology - Applied Microbiology |
| Principal Investigator: | Eliana Gertrudes de Macedo Lemos |
| Grantee: | Bruna Castro |
| Home Institution: | Faculdade de Ciências Agrárias e Veterinárias (FCAV). Universidade Estadual Paulista (UNESP). Campus de Jaboticabal. Jaboticabal , SP, Brazil |
Abstract The soil has great diversity of microorganisms. This group is known for its ability to produce many secondary compounds, among them highlight the production of antibiotics, that have a great pharmacological importance. However, its not possible access the full biotechnological potential of the microbiota, because the cultivation methods used in laboratories usually select microorganisms. Thus, the vast majority of soil bacteria, about 99%, cannot be isolated or grown in culture media, since they have such complex needs that cannot be reproduced artificially. Because of this, Metagenomics, the genomic analysis of unculturable microorganisms, allows wider access to genetic and biochemical potential of the microbiota. It allows the description of the metabolism of unknown bacteria, development of phylogenetic hypotheses, studies of ecological relationships, analysis of biodiversity, besides the discovery of unknown microorganisms and the development of new bioactive compounds. Among the biomolecules known, can highlight the polyketide antibiotics, which are biosynthesized by enzymatic groups called Polyketide Synthases (PKS), that may be types I, II and III, in addition to hybrid PKS-NRPS pathways, that include enzymes clustered with PKS pathways "nonribosomal peptide synthetases", responsible for the synthesis of amino acids linked to special polyketides. This research project aims to analyze the diversity of new pathways for antibiotic PKSs systems I, II and PKS-NRPS in metagenomic libraries, employing polimerase chain reaction technique. | |