View source for 8hp2


==CtPDC==
<StructureSection load='8hp2' size='340' side='right'caption='[[8hp2]], [[Resolution|resolution]] 3.05&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[8hp2]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Candida_tropicalis Candida tropicalis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8HP2 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8HP2 FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.05&#8491;</td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8hp2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8hp2 OCA], [https://pdbe.org/8hp2 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8hp2 RCSB], [https://www.ebi.ac.uk/pdbsum/8hp2 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8hp2 ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/C5MDS4_CANTT C5MDS4_CANTT] 
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Tyrosol is an important chemical in medicine and chemical industries, which can be synthesized by a four-enzyme cascade pathway constructed in our previous study. However, the low catalytic efficiency of pyruvate decarboxylase from Candida tropicalis (CtPDC) in this cascade is a rate-limiting step. In this study, we resolved the crystal structure of CtPDC and investigated the mechanism of allosteric substrate activation and decarboxylation of this enzyme toward 4-hydroxyphenylpyruvate (4-HPP). In addition, based on the molecular mechanism and structural dynamic changes, we conducted protein engineering of CtPDC to improve decarboxylation efficiency. The conversion of the best mutant, CtPDC(Q112G/Q162H/G415S/I417V) (CtPDC(Mu5)), had over two-fold improvement compared to the wild-type. Molecular dynamic (MD) simulation revealed that the key catalytic distances and allosteric transmission pathways were shorter in CtPDC(Mu5) than in the wild type. Furthermore, when CtPDC in the tyrosol production cascade was replaced with CtPDC(Mu5), the tyrosol yield reached 38 g.L(-1) with 99.6% conversion and 1.58 g.L(-1).h(-1) space-time yield in 24 h through further optimization of the conditions. Our study demonstrates that protein engineering of the rate-limiting enzyme in the tyrosol synthesis cascade provides an industrial-scale platform for the biocatalytic production of tyrosol. KEY POINTS: * Protein engineering of CtPDC based on allosteric regulation improved the catalytic efficiency of decarboxylation. * The application of the optimum mutant of CtPDC removed the rate-limiting bottleneck in the cascade. * The final titer of tyrosol reached 38 g.L(-1) in 24 h in 3 L bioreactor.

Improving tyrosol production efficiency through shortening the allosteric signal transmission distance of pyruvate decarboxylase.,Xu H, Yu B, Wei W, Chen X, Gao C, Liu J, Guo L, Song W, Liu L, Wu J Appl Microbiol Biotechnol. 2023 Jun;107(11):3535-3549. doi: , 10.1007/s00253-023-12540-1. Epub 2023 Apr 26. PMID:37099057<ref>PMID:37099057</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 8hp2" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Candida tropicalis]]
[[Category: Large Structures]]
[[Category: Song W]]
[[Category: Xu HH]]