Construction of a mutant library of horseradish peroxidase gene by directed evolution and development of an in situ screening method
| Autor: | Héctor M. Targovnik, Fernando Mendive, O. Cascone, M.V. Miranda, M.M. Segura |
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| Rok vydání: | 2003 |
| Předmět: |
Gel electrophoresis
biology horseradish peroxidase General Chemical Engineering lcsh:TP155-156 Directed evolution Molecular biology Horseradish peroxidase law.invention DNA shuffling chemistry.chemical_compound chemistry law mutant library biology.protein Recombinant DNA Agarose lcsh:Chemical engineering directed evolution Polymerase chain reaction Peroxidase |
| Zdroj: | Brazilian Journal of Chemical Engineering, Volume: 20, Issue: 1, Pages: 33-38, Published: MAR 2003 Brazilian Journal of Chemical Engineering, Vol 20, Iss 1, Pp 33-38 (2003) Brazilian Journal of Chemical Engineering v.20 n.1 2003 Brazilian Journal of Chemical Engineering Associação Brasileira de Engenharia Química (ABEQ) instacron:ABEQ |
| ISSN: | 0104-6632 |
| DOI: | 10.1590/s0104-66322003000100007 |
| Popis: | A process of directed evolution applied to obtain a library of mutants of horseradish peroxidase (HRP) enzyme is described. We have introduced slight variations into the original DNA shuffling protocol. A DNA template was prepared by PCR amplification and digested with Dnase I during 1 hour. Dnase I products were concentrated by precipitation with isopropanol. Gel electrophoresis showed fragments of the desired size range (20-600 pb) without a full-length template remaining in the reaction mixture. A high concentration of fragments was crucial for performing PCR without primers. In this case, a template concentration of 32.5 ng/mu l was appropriate. Amplification of recombinant genes in a standard PCR reaction (template dilution 1:100) produced a smear with a low yield for the full-length sequence. A single product of the correct size was obtained by PCR with nested primers separated from the previously used primers by 40 pb. In our laboratory, native HRP has been functionally expressed in a baculovirus expression vector system. The purpose is to develop the screening of the first generation of random mutants in this system. To facilitate detection of those clones that have high peroxidase activity, we developed a rapid method: after five days postinfection agarose plates with six wells were covered with DAB (3,3´-diaminobenzidine) and H2O2. The appearance of brown-black stain allows visualization of up to 100 active clones/well in only 1 min. |
| Databáze: | OpenAIRE |
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