This is a page describing data taken during an experiment at the ISIS Neutron and Muon Source. Information about the ISIS Neutron and Muon Source can be found at https://www.isis.stfc.ac.uk.
Investigation of the Dynamic Mechanism of Xylanase by QENS
Abstract: In this proposal we will pioneer the use of QENS in combination with molecular biology mutagenesis and in silico design to guide the re-engineering of a glycoside hydrolase, xylanase, to allow for more efficient hydrolysis of hemicellulose to xylose over a broader range of conditions. Our previous X-ray and neutron crystallography results show that a catalytic active glutamate residue has alternate conformations to transfer proton to cleave the glycosidic bond. This activity is temperature and pH dependent. However, crystallography could only give snapshot information of structure, not dynamics. Therefore we aim to study how the activity is associated with temperature and pH using QENS. This information will be used to guide in silico enzyme engineerin leading to rational mutagenesis studies in order to increase catalytic activity at higher temperature and pH.
Principal Investigator: Professor Xiangqiang Chu
Local Contact: Dr Victoria Garcia Sakai
Experimenter: Dr Qun Wan
Experimenter: Mr Zhixin Wang
Experimenter: Mr Xudong Gu
Experimenter: Mr Shengkai Zhang
Experimenter: Miss jingjing Han
DOI: 10.5286/ISIS.E.RB1920317
ISIS Experiment Number: RB1920317
Part DOI | Instrument | Public release date | Download Link |
---|---|---|---|
10.5286/ISIS.E.RB1920317-1 | IRIS | 13 October 2022 | Download |
Publisher: STFC ISIS Neutron and Muon Source
Data format: RAW/Nexus
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Data Citation
The recommended format for citing this dataset in a research
publication is as:
[author], [date], [title], [publisher],
[doi]
For Example:
Professor Xiangqiang Chu et al; (2019): Investigation of the Dynamic Mechanism of Xylanase by QENS, STFC ISIS Neutron and Muon Source, https://doi.org/10.5286/ISIS.E.RB1920317
Data is released under the CC-BY-4.0 license.