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Identification and characterization of novel poly(DL-lactic acid) depolymerases from metagenome.
- Source :
-
Applied microbiology and biotechnology [Appl Microbiol Biotechnol] 2008 Jul; Vol. 79 (5), pp. 743-50. Date of Electronic Publication: 2008 May 07. - Publication Year :
- 2008
-
Abstract
- Many poly(lactic acid) (PLA)-degrading microorganisms have been isolated from the natural environment by culture-based methods, but there is no study about unculturable PLA-degrading microorganisms. In this study, we constructed a metagenomic library consisting of the DNA extracted from PLA disks buried in compost. We identified three PLA-degrading genes encoding lipase or hydrolase. The purified enzymes degraded not only PLA, but also various aliphatic polyesters, tributyrin, and p-nitrophenyl esters. From their substrate specificities, the PLA depolymerases were classified into an esterase rather than a lipase. Among the PLA depolymerases, PlaM4 exhibited thermophilic properties; that is, it showed the highest activity at 70 degrees C and was stable even after incubation for 1 h at 50 degrees C. PlaM4 had absorption and degradation activities for solid PLA at 60 degrees C, which indicates that the enzyme can effectively degrade PLA in a high-temperature environment. On the other hand, the enzyme classification based on amino acid sequences showed that the other PLA depolymerases, PlaM7 and PlaM9, were not classified into known lipases or esterases. This is the first report on the identification and characterization of PLA depolymerase from a metagenome.
- Subjects :
- Bacteria chemistry
Bacteria classification
Bacteria genetics
Bacterial Proteins isolation & purification
Bacterial Proteins metabolism
Biodiversity
Cloning, Molecular
Enzyme Stability
Esterases isolation & purification
Esterases metabolism
Gene Library
Lipase chemistry
Lipase genetics
Lipase isolation & purification
Lipase metabolism
Molecular Sequence Data
Phylogeny
Polyesters
Sequence Analysis, DNA
Soil Microbiology
Substrate Specificity
Bacteria enzymology
Bacterial Proteins chemistry
Bacterial Proteins genetics
Esterases chemistry
Esterases genetics
Genome, Bacterial
Lactic Acid metabolism
Polymers metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0175-7598
- Volume :
- 79
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Applied microbiology and biotechnology
- Publication Type :
- Academic Journal
- Accession number :
- 18461319
- Full Text :
- https://doi.org/10.1007/s00253-008-1477-3