| Title : Protocol for in-vitro purification and refolding of hexachlorocyclohexane degrading enzyme haloalkane dehalogenase LinB from inclusion bodies - Kaur_2021_Enzyme.Microb.Technol_146_109760 |
| Author(s) : Kaur J , Singh A , Panda AK , Lal R |
| Ref : Enzyme Microb Technol , 146 :109760 , 2021 |
| Abstract : LinB is an important haloalkane dehalogenase involved in the degradation pathway of different isomers of hexachlorocyclohexane (HCH), mainly in catalyzing degradation of the notorious beta-HCH. The HCH isomers are known to have neurotoxic, carcinogenic and estrogenic effects. Enzymatic bioremediation for decontamination of beta- as well as other HCH isomers can prove to be a potential remediation strategy. For any bioremediation technology that is to be developed, apart from having high turnover number, the candidate enzyme must also be available in sufficient amounts. In this direction, the LinB variants reported in database were tested in laboratory studies. The variant LinBSSO4-3 however could not be obtained in soluble fraction by using standard procedures. The protein LinBSSO4-3 was cloned in pDEST17 vector and codon optimized for better expression in Escherichia coli BL21AI using a strong T7 promoter. However, the over-expression of this protein in ectopic host E. coli, led to aggregation of the protein in form of inclusion bodies, which are insoluble aggregates of misfolded or partially folded proteins. SEM analysis of the inclusion bodies showed them as aggregated spherical particles. The inclusion bodies were isolated using high speed sonication and homogenization. This was followed by solubilization in the strong denaturing agent urea. Refolding into its native state was done by using pulsatile refolding. This was done by slowly decreasing the denaturant concentration in the presence of sucrose. The turnover number of the refolded protein was then determined for different isomers of HCH. The protein was found to have a turnover number of -43 molecules min(-1) on beta-HCH and -13 molecules min(-1) on delta-HCH. Additionally, a mutation I253 M in the active site of the enzyme was found to drastically decrease the enzyme activity on beta-HCH. Taking into consideration the wide range of substrates of haloalkane dehalogenases, such a protocol for inclusion body refolding will contribute to the field of bioremediation technology development for organochlorines, specifically HCH. Such a protocol for refolding of haloalkane dehalogenases from inclusion bodies has not been developed or reported before. |
| ESTHER : Kaur_2021_Enzyme.Microb.Technol_146_109760 |
| PubMedSearch : Kaur_2021_Enzyme.Microb.Technol_146_109760 |
| PubMedID: 33812559 |
| Gene_locus related to this paper: sphpi-linb |
| Gene_locus related to this paper: sphpi-linb |
Kaur J, Singh A, Panda AK, Lal R (2021)
Protocol for in-vitro purification and refolding of hexachlorocyclohexane degrading enzyme haloalkane dehalogenase LinB from inclusion bodies
Enzyme Microb Technol
146 :109760
Kaur J, Singh A, Panda AK, Lal R (2021)
Enzyme Microb Technol
146 :109760