Production of biologically active recombinant human lactoferrin in aspergillus oryzae

Pauline P. Ward, Jing Y. Lo, Mairead Duke, Gregory S. May, Denis R. Headon, Orla M. Conneely

Research output: Contribution to journalArticlepeer-review

100 Scopus citations

Abstract

We report the production of recombinant human lactoferrin in Aspergillus oryzae. Expression of human lactoferrin (hLF), a 78 kD glycoprotein, was achieved by placing the cDNA under the control of the A. oryzae a - amylase promoter and the 3’ flanking region of the A. niger glucoamylase gene. Using this system, hLF is expressed and secreted into the growth medium at levels up to 25 mg/l. The recombinant lactoferrin is indistinguishable from human milk lactoferrin with respect to its size, immunoreactivity, and iron - binding capacity. The recombinant protein appears to be appropriately N - linked glycosylated and correctly processed at the N - terminus by the A. oryzae secretory apparatus. Lactoferrin is the largest heterologous protein and the first mammalian glycoprotein expressed in the Aspergillus system to date. Hence, this expression system appears suitable for the large - scale production and secretion of biologically active mammalian glycoproteins.

Original languageEnglish (US)
Pages (from-to)784-789
Number of pages6
JournalBio/Technology
Volume10
Issue number7
DOIs
StatePublished - Jul 1992

ASJC Scopus subject areas

  • Biotechnology

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