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Cloning, Expression and Purification of Halophilic Lipase from Micrococcus luteus
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.advisor | Kwon-Young Choi | - |
| dc.contributor.author | JOHNSON, JERVIAN JERDIAN | - |
| dc.date.accessioned | 2018-11-08T08:23:56Z | - |
| dc.date.available | 2018-11-08T08:23:56Z | - |
| dc.date.issued | 2017-08 | - |
| dc.identifier.other | 26054 | - |
| dc.identifier.uri | https://dspace.ajou.ac.kr/handle/2018.oak/13590 | - |
| dc.description | 학위논문(석사)--아주대학교 일반대학원 :환경공학과,2017. 8 | - |
| dc.description.tableofcontents | 1. Introduction 1 2. Method 6 2.1 Cloning of Lipase genes 6 2.2 Bacterial strains and plasmid 6 2.3 Growth Conditions 6 2.4 DNA Manipulation, Sequence Analyses and structure homologies 7 2.5 Preparation of plasmid constructs for the expression of BVMOs 7 2.6 Optimization of MLu_Lip1 Sequence 8 2.7 Homologous Expression of Lipase 8 2.8 SDS-PAGE Analysis 9 2.9 Protein Expression Optimization 9 2.9.1 Reducing the IPTG Concentration 10 2.9.2 Growth Medium 10 2.9.3 Coexpression of MLu_Lip1 with molecular chaperones in E.coli BL21 (DE3) 10 2.10 Expression of MLu_Lip1 in the presence of chemical chaperones 11 2.11 Purification of MLu_Lip1 grown at optimum conditions 11 2.12 Removal of Periplasmic Fraction by Osmotic Shock 12 2.13 Purification After Osmotic Shock 13 2.14 Bradford Protein Analyses 13 2.15 Lipase Activity Assay 14 2.16 Esterase Activity Assay 14 3. Results 15 3.1 Cloning of Lipase genes 15 3.2 Homologous Expression of Lipase 15 3.3 Protein expression optimization 18 3.4 Purification of MLu_Lip1 using optimum growth conditions 22 3.5 Protein and Activity Analyses 26 4. Discussion 28 5. Conclusion and Future Prospects 31 6. References 32 (Attachment 1) 35 | - |
| dc.language.iso | eng | - |
| dc.publisher | The Graduate School, Ajou University | - |
| dc.rights | 아주대학교 논문은 저작권에 의해 보호받습니다. | - |
| dc.title | Cloning, Expression and Purification of Halophilic Lipase from Micrococcus luteus | - |
| dc.type | Thesis | - |
| dc.contributor.affiliation | 아주대학교 일반대학원 | - |
| dc.contributor.department | 일반대학원 환경공학과 | - |
| dc.date.awarded | 2017. 8 | - |
| dc.description.degree | Master | - |
| dc.identifier.localId | 788497 | - |
| dc.identifier.url | http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000026054 | - |
| dc.subject.keyword | Halophilic | - |
| dc.subject.keyword | lipase | - |
| dc.subject.keyword | lipase activity | - |
| dc.subject.keyword | enzyme | - |
| dc.subject.keyword | DNA cloning | - |
| dc.subject.keyword | protein purification | - |
| dc.description.alternativeAbstract | Lipase is an enzyme that catalyzes the hydrolysis of triglycerides and fatty acids and has diverse applications in the biochemical industry. Lipase is currently used for catalyzing reactions in the food, oil and fat, detergent, leather, pulp and paper, and cosmetic industries; as well as in biodiesel production and organic chemistry. As such, cloning and purifying lipase displaying attractive properties is important. Lipase from the halophilic bacterium Micrococcus luteus was selected for cloning and purification because of its excellent salt resistance properties (reported by J. Johnson et. al). That is, it displayed a salt resistance of 2M NaCl, which is over 3 times higher than that of sea water. During the cloning and purification process, there were challenges that were encountered. Firstly, the size of the gene is small compared to the genomic DNA (800 bp compared to 3.86 Mbp) making primers that were designed less effective. However, using a combination of forward and reverse primers, the lipase gene was successfully cloned and determined to be 800 base pairs (bp). In addition, due to the incompatibility of M. luteus and E. coli BL21 (DE3)'s triplet coding, expression of the protein was also difficult. However, with optimization of the coding sequence for M. luteus lipase, it was successfully expressed and the protein was determined to be 35 kilo Daltons (kD) in size. The level of protein expression was low and as such various methods were employed in an effort to improve the amount of lipase expressed. These include: variation of IPTG concentration at induction; co-expression of lipase gene with vector chaperones; culturing the cells containing the recombinant gene using various growth media; and applying a wide range of chemical chaperones to the cell cultures. Through the optimization experiments it was determined that when the lipase gene was co-expressed with pG-Tf16 vector chaperone and grown with Reseinberg medium and Magnesium Chloride and induced at 0.05mM IPTG, optimum lipase expression was achieved. The gene was later purified using heat shock and immobilized metal-affinity chromatography (IMAC) methods. The activity of the lipase gene was tested using lipase and esterase assays. The lipase activity was determined to be 553.35 U/mg when tested with substrate, p-nitrophenylpalmitate (pNPP). This was compared to the activity of commercial lipase (lipase from Candida rugosa), which produced a specific activity of 25.66 U/mg, indicating that the lipase from M. luteus has comparatively excellent activity. Esterase activity was however not detected in lipase from M. luteus when p-nitrophenylbutyrate (pNPB) was used as the substrate. Based on the high lipase activity obtained through experiments, it is fair to say that the cloned and purified lipase from this research has commercial potential. Further research is however necessary to characterize the lipase and produce it in a form that allows it to be applied industrially. | - |
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