Rational design of a carboxylic esterase RhEst1 based on computational analysis of substrate binding

Journal Article · Sat Oct 31 00:00:00 EDT 2015 · Journal of Molecular Graphics and Modelling

DOI:https://doi.org/10.1016/j.jmgm.2015.10.015· OSTI ID:1327643

Chen, Qi ^[1]; Luan, Zheng -Jiao ^[1]; Yu, Hui -Lei ^[1]; Cheng, Xiaolin ^[2]; Xu, Jian -He ^[1]

---

1. East China Univ. of Science and Technology, Shanghai (China)
2. Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Univ. of Tennessee, Knoxville, TN (United States)

A new carboxylic esterase RhEst1 which catalyzes the hydrolysis of (S)-(+)-2,2-dimethylcyclopropanecarboxylate (S-DmCpCe), the key chiral building block of cilastatin, was identified and subsequently crystallized in our previous work. Mutant RhEst_{1A147I/V148F/G254A} was found to show a 5-fold increase in the catalytic activity. In this work, molecular dynamic simulations were performed to elucidate the molecular determinant of the enzyme activity. Our simulations show that the substrate binds much more strongly in the A147I/V148F/G254A mutant than in wild type, with more hydrogen bonds formed between the substrate and the catalytic triad and the oxyanion hole. The OH group of the catalytic residue Ser101 in the mutant is better positioned to initiate the nucleophilic attack on S-DmCpCe. Interestingly, the "170-179" loop which is involved in shaping the catalytic sites and facilitating the product release shows remarkable dynamic differences in the two systems. Based on the simulation results, six residues were identified as potential "hot-spots" for further experimental testing. Consequently, the G126S and R133L mutants show higher catalytic efficiency as compared with the wild type. In conclusion, this work provides molecular-level insights into the substrate binding mechanism of carboxylic esterase RhEst1, facilitating future experimental efforts toward developing more efficient RhEst1 variants for industrial applications.

• Research Organization: Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)
• Sponsoring Organization: USDOE
• Grant/Contract Number: AC05-00OR22725; De-AC05-00OR22725
• OSTI ID: 1327643
• Alternate ID(s): OSTI ID: 1432567
• Journal Information: Journal of Molecular Graphics and Modelling, Vol. 62, Issue C; ISSN 1093-3263
• Publisher: Elsevier
• Country of Publication: United States
• Language: English

Related Subjects

59 BASIC BIOLOGICAL SCIENCES
carboxylic esterase
molecular dynamics simulation
rational design
structural mechanism
catalytic efficiency