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Published on: November 23, 2016
Lactobacillus sps. lipase mediated poly (ε-caprolactone) degradation
Imran Khan1, Jayati Ray Dutta1, Ramakrishnan Ganesan2
1Department of Biological Sciences, BITS Pilani, Hyderabad Campus, Jawahar Nagar, Shameerpet Mandal, Hyderabad 500078, Telangana, India.
Enzymatic degradation of poly (ε-caprolactone) (PCL) using lipases from Lactobacillus offers a sustainable alternative to chemical methods. This study explored enzyme efficiency and degradation mechanisms.
Area of Science:
- Biotechnology
- Polymer Science
- Microbiology
Background:
- Polymer degradation via enzymatic routes is a sustainable alternative to chemical processes.
- Poly (ε-caprolactone) (PCL) is an industrially relevant polyester susceptible to microbial and enzymatic breakdown.
- Bacterial lipases and esterases play a key role in the environmental degradation of PCL.
Purpose of the Study:
- To investigate the efficiency of three distinct lipases from Lactobacillus brevis, Lactobacillus plantarum, and their co-culture in degrading PCL.
- To analyze the impact of enzyme loading and degradation time on PCL enzymatic degradation.
- To gain mechanistic insights into the PCL enzymatic degradation process.
Main Methods:
- Enzymatic degradation assays using purified lipases.
- Thermogravimetric analysis (TGA) and differential thermal analysis (DTA) for material characterization.
- Scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) for analyzing degradation.
Main Results:
- The study successfully demonstrated the enzymatic degradation of PCL using the selected lipases.
- Optimization of enzyme loading and degradation time influenced the degradation rate and extent.
- Characterization techniques provided insights into the surface morphology and chemical changes of PCL during degradation.
Conclusions:
- Lipase-mediated degradation of PCL presents a viable and eco-friendly approach.
- Lactobacillus-derived lipases show potential for controlled PCL biodegradation.
- Further research can optimize enzymatic conditions for enhanced PCL degradation applications.
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