Literature DB >> 15046591

Application of thermophilic enzymes in commercial biotransformation processes.

I N Taylor1, R C Brown, M Bycroft, G King, J A Littlechild, M C Lloyd, C Praquin, H S Toogood, S J C Taylor.   

Abstract

Biocatalysis is a useful tool in the provision of chiral technology and extremophilic enzymes are just one component in that toolbox. Their role is not always attributable to their extremophilic properties; as with any biocatalyst certain other criteria should be satisfied. Those requirements for a useful biocatalyst will be discussed including issues of selectivity, volume efficiency, security of supply, technology integration, intellectual property and regulatory compliance. Here we discuss the discovery and commercialization of an L-aminoacylase from Thermococcus litoralis, the product of a LINK project between Chirotech Technology and the University of Exeter. The enzyme was cloned into Escherichia coli to aid production via established mesophilic fermentation protocols. A simple downstream process was then developed to assist in the production of the enzyme as a genetically modified-organism-free reagent. The fermentation and downstream processes are operated at the 500 litre scale. Characterization of the enzyme demonstrated a substrate preference for N-benzoyl groups over N-acetyl groups. The operational parameters have been defined in part by substrate-concentration tolerances and also thermostability. Several examples of commercial biotransformations will be discussed including a process that is successful by virtue of the enzyme's thermotolerance.

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Year:  2004        PMID: 15046591     DOI: 10.1042/bst0320290

Source DB:  PubMed          Journal:  Biochem Soc Trans        ISSN: 0300-5127            Impact factor:   5.407


  3 in total

Review 1.  Enzyme immobilization: an update.

Authors:  Ahmad Abolpour Homaei; Reyhaneh Sariri; Fabio Vianello; Roberto Stevanato
Journal:  J Chem Biol       Date:  2013-08-29

2.  Identification of poly(cis-1,4-Isoprene) degradation intermediates during growth of moderately thermophilic actinomycetes on rubber and cloning of a functional lcp homologue from Nocardia farcinica strain E1.

Authors:  Ebaid M A Ibrahim; Matthias Arenskötter; Heinrich Luftmann; Alexander Steinbüchel
Journal:  Appl Environ Microbiol       Date:  2006-05       Impact factor: 4.792

3.  Cloning, expression, and characterization of aminopeptidase P from the hyperthermophilic archaeon Thermococcus sp. strain NA1.

Authors:  Hyun Sook Lee; Yun Jae Kim; Seung Seob Bae; Jeong Ho Jeon; Jae Kyu Lim; Byeong Chul Jeong; Sung Gyun Kang; Jung-Hyun Lee
Journal:  Appl Environ Microbiol       Date:  2006-03       Impact factor: 4.792

  3 in total

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