Bacteria and actinomycetes were screened for esterase enzymes capable of removing the para-nitrobenzyl ester from cephalosporins. An esterase preparation from Bacillus subtilis was used to prepare cephalexin and 7-ADCA from the corresponding para-nitrobenzyl esters.
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http://dx.doi.org/10.7164/antibiotics.29.121 | DOI Listing |
Biotechnol Rep (Amst)
June 2024
Queensland University of Technology (QUT), The School of Biology and Environmental Science (BES), 2 George St Brisbane, QLD 4001, Australia.
Phthalate esters are known to be endocrine disrupting chemicals and are documented to pollute environments. Enzymatic degradation of PAEs is a potential bioremedial strategy to manage contamination. Thermostable bioremedial enzymes have advantages in enzyme manufacturing and storage.
View Article and Find Full Text PDFRSC Adv
April 2023
Hangzhou Hyproven Biopharm Co.,Ltd. Hangzhou 311107 China
J Mol Biol
March 2003
Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125-0001, USA.
Molecular dynamics simulations were employed to study how protein solution structure and dynamics are affected by adaptation to high temperature. Simulations were carried out on a para-nitrobenzyl esterase (484 residues) and two thermostable variants that were generated by laboratory evolution. Although these variants display much higher melting temperatures than wild-type (up to 18 degrees C higher) they are both >97% identical in sequence to the wild-type.
View Article and Find Full Text PDFJ Mol Biol
September 1997
Division of Chemistry, California Institute of Technology, Pasadena, CA 91125, USA.
Sets of genes improved by directed evolution can be recombined in vitro to produce further improvements in protein function. Recombination is particularly useful when improved sequences are available; costs of generating such sequences, however, must be weighed against the costs of further evolution by sequential random mutagenesis. Four genes encoding para-nitrobenzyl (pNB) esterase variants exhibiting enhanced activity were recombined in two cycles of high-fidelity DNA shuffling and screening.
View Article and Find Full Text PDFAdv Biochem Eng Biotechnol
May 1997
Division of Chemistry and Chemical Engineering 210-41, California Institute of Technology, Pasadena 91125, USA.
Enzymes can be tailored for optimal performance in industrial applications by directing their evolution in vitro. This approach is particularly attractive for engineering industrial enzymes. We have created an efficient para-nitrobenzyl esterase over six generations of random point mutagenesis and recombination coupled with screening for improved variants.
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