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Scalable High-Performance Production of Recombinant Horseradish Peroxidase from E. coli Inclusion Bodies.


ABSTRACT: Horseradish peroxidase (HRP), an enzyme omnipresent in biotechnology, is still produced from hairy root cultures, although this procedure is time-consuming and only gives low yields. In addition, the plant-derived enzyme preparation consists of a variable mixture of isoenzymes with high batch-to-batch variation preventing its use in therapeutic applications. In this study, we present a novel and scalable recombinant HRP production process in Escherichia coli that yields a highly pure, active and homogeneous single isoenzyme. We successfully developed a multi-step inclusion body process giving a final yield of 960 mg active HRP/L culture medium with a purity of ≥99% determined by size-exclusion high-performance liquid chromatography (SEC-HPLC). The Reinheitszahl, as well as the activity with 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) and 3,3',5,5'-tetramethylbenzidine (TMB) as reducing substrates, are comparable to commercially available plant HRP. Thus, our preparation of recombinant, unglycosylated HRP from E. coli is a viable alternative to the enzyme from plant and highly interesting for therapeutic applications.

SUBMITTER: Humer D 

PROVIDER: S-EPMC7369975 | biostudies-literature | 2020 Jun

REPOSITORIES: biostudies-literature

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Scalable High-Performance Production of Recombinant Horseradish Peroxidase from <i>E. coli</i> Inclusion Bodies.

Humer Diana D   Ebner Julian J   Spadiut Oliver O  

International journal of molecular sciences 20200629 13


Horseradish peroxidase (HRP), an enzyme omnipresent in biotechnology, is still produced from hairy root cultures, although this procedure is time-consuming and only gives low yields. In addition, the plant-derived enzyme preparation consists of a variable mixture of isoenzymes with high batch-to-batch variation preventing its use in therapeutic applications. In this study, we present a novel and scalable recombinant HRP production process in <i>Escherichia coli</i> that yields a highly pure, act  ...[more]

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