Enhanced citrate production through gene insertion in Aspergillus niger

Wian de Jongh, Jens Nielsen

    Research output: Contribution to journalJournal articleResearchpeer-review

    Abstract

    The effect of inserting genes involved in the reductive branch of the tricarboxylic acid (TCA) cycle on citrate production by Aspergillus niger was evaluated. Several different genes were inserted individually and in combination, i.e. malate dehydrogenase (mdh2) from Saccharomyces cerevisiae, two truncated, cytosolic targeted, fumarases (Fum1s and FumRs) from S. cerevisiae and Rhizopus oryzae, respectively, and the cytosolic soluble fumarate reductase (Frds1) from S. cerevisiae. Overexpression of these genes in their native strain backgrounds has been reported to lead to alterations in the intracellular cytosolic dicarboxylate concentrations. It was found that all the transformant strains had enhanced yield and productivities of citrate compared with the wild-type strain. The transformants also had the ability to produce citrate in trace-manganese-contaminated medium, where the wild type was unable to produce. Overexpression of FumRs and Frds1 resulted in the best citrate-producing strain in the presence of trace manganese concentrations. This strain gave a maximum yield of 0.9 g citrate per g glucose and a maximum specific productivity of 0.025 g citrate per g DW per h. Overexpression of mdh2 alone resulted in an increased citrate production rate only in the initial phase of the fermentations compared with the other transformants and the wild type. (C) 2007 Elsevier Inc. All rights reserved.
    Original languageEnglish
    JournalMetabolic Engineering
    Volume10
    Issue number2
    Pages (from-to)87-96
    ISSN1096-7176
    DOIs
    Publication statusPublished - 2007

    Fingerprint Dive into the research topics of 'Enhanced citrate production through gene insertion in Aspergillus niger'. Together they form a unique fingerprint.

    Cite this