Ibrahim Ali, Noorbatcha and Hamzah, Mohd. Salleh (2017) Ultra-high-throughput screening of beta glucoside kinase random mutagenesis library for phosphorus-sulfur bond Formation. In: KUALA LUMPUR, Putrajaya Marriott Hotel, Malaysia. (Unpublished)
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Abstract
Abstract. In the continual quest of novel biocatalysts with improved properties that will fulfil the raising industrial demands, directed evolution appears to be one of the most powerful tools in generating novel enzymes. Error -Prone PCR is a customized PCR protocol that will randomly introduce mutations creating a variant library. Beta glucoside kinase (bglk) is an enzyme that catalyzes the phosphor transformation to the 6’ C in a glucose molecule. The aim of the presented research is to engineer the bglk enzyme for phosphorus-sulfur bond formation. Two bglk libraries were created, one with a low mutation rate (0-4 mutation/kb) and the second with high mutation rate (9-16 mutation/kb) and was screened with Fluorescent Activated Cell Sorting (FACS) using a 6’thio-glucose-BODIPY as fluorescent substrate. Prior to this, a Glucose-BODIPY substrate was used with the wild type enzyme in order to test the cell incubation conditions with the fluorescent substrate. The positive clones collected from these two libraries, will be sequenced to verify the type and location of the mutations.
Item Type: | Conference or Workshop Item (Slide Presentation) |
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Additional Information: | 3704/61791 |
Subjects: | T Technology > TP Chemical technology > TP248.13 Biotechnology |
Kulliyyahs/Centres/Divisions/Institutes (Can select more than one option. Press CONTROL button): | Kulliyyah of Engineering > Department of Biotechnology Engineering |
Depositing User: | Prof. Dr. Ibrahim Ali Noorbatcha |
Date Deposited: | 03 Feb 2018 16:54 |
Last Modified: | 03 Feb 2018 16:55 |
URI: | http://irep.iium.edu.my/id/eprint/61791 |
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