Noby_2021_Open.Biol_11_210182

Reference

Title : Structure and in silico simulations of a cold-active esterase reveals its prime cold-adaptation mechanism - Noby_2021_Open.Biol_11_210182
Author(s) : Noby N , Auhim HS , Winter S , Worthy HL , Embaby AM , Saeed H , Hussein A , Pudney CR , Rizkallah PJ , Wells SA , Jones DD
Ref : Open Biol , 11 :210182 , 2021
Abstract : Here we determined the structure of a cold active family IV esterase (EstN7) cloned from Bacillus cohnii strain N1. EstN7 is a dimer with a classical alpha/beta hydrolase fold. It has an acidic surface that is thought to play a role in cold-adaption by retaining solvation under changed water solvent entropy at lower temperatures. The conformation of the functionally important cap region is significantly different to EstN7's closest relatives, forming a bridge-like structure with reduced helical content providing greater access to the active site through more than one substrate access tunnel. However, dynamics do not appear to play a major role in cold adaption. Molecular dynamics at different temperatures, rigidity analysis, normal mode analysis and geometric simulations of motion confirm the flexibility of the cap region but suggest that the rest of the protein is largely rigid. Rigidity analysis indicates the distribution of hydrophobic tethers is appropriate to colder conditions, where the hydrophobic effect is weaker than in mesophilic conditions due to reduced water entropy. Thus, it is likely that increased substrate accessibility and tolerance to changes in water entropy are important for of EstN7's cold adaptation rather than changes in dynamics.
ESTHER : Noby_2021_Open.Biol_11_210182
PubMedSearch : Noby_2021_Open.Biol_11_210182
PubMedID: 34847772
Gene_locus related to this paper: 9baci-a0a2k9uv39

Related information

Gene_locus related to this paper: 9baci-a0a2k9uv39

Citations formats

Noby N, Auhim HS, Winter S, Worthy HL, Embaby AM, Saeed H, Hussein A, Pudney CR, Rizkallah PJ, Wells SA, Jones DD (2021)
Structure and in silico simulations of a cold-active esterase reveals its prime cold-adaptation mechanism
Open Biol 11 :210182

Noby N, Auhim HS, Winter S, Worthy HL, Embaby AM, Saeed H, Hussein A, Pudney CR, Rizkallah PJ, Wells SA, Jones DD (2021)
Open Biol 11 :210182