Literature DB >> 22539024

Variation of the by-product spectrum during α-ketoglutaric acid production from raw glycerol by overexpression of fumarase and pyruvate carboxylase genes in Yarrowia lipolytica.

Christina Otto1, Venelina Yovkova, Andreas Aurich, Stephan Mauersberger, Gerold Barth.   

Abstract

The yeast Yarrowia lipolytica secretes high amounts of various organic acids, like citric, isocitric, pyruvic (PA), and α-ketoglutaric (KGA) acids, triggered by growth limitation and excess of carbon source. This is leading to an increased interest in this non-conventional yeast for biotechnological applications. To improve the KGA production by Y. lipolytica for an industrial application, it is necessary to reduce the amounts of by-products, e.g., fumarate (FU) and PA, because production of by-products is a main disadvantage of the KGA production by this yeast. We have examined whether the concentration of secreted organic acids (main product KGA and PA as major by-product and FU, malate (MA), and succinate (SU) as minor by-products) can be influenced by a gene-dose-dependent overexpression of fumarase (FUM) or pyruvate carboxylase (PYC) genes under KGA production conditions. Recombinant Y. lipolytica strains were constructed, which harbor multiple copies of the respective FUM1, PYC1 or FUM1, and PYC1 genes. Overexpression of the genes FUM1 and PYC1 resulted in strongly increased specific enzyme activities during cultivation of these strains on raw glycerol as carbon source in bioreactors. The recombinant Y. lipolytica strains showed different product selectivity of the secreted organic acids KGA, PA, FU, MA, and SU. Concentrations of the by-products FU, MA, SU, and PA decreased significantly at overproduction of FUM and increased at overproduction of PYC and also of FUM and PYC simultaneously. In contrast, the production of KGA with the multicopy strains H355A(FUM1) and H355A(FUM1-PYC1) was comparable with the wild-type strain H355 or slightly lower in case of H355(PYC1). KGA productivity was not changed significantly compared with strain H355 whereas product selectivity of the main product KGA was increased in H355A(FUM1).

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Year:  2012        PMID: 22539024     DOI: 10.1007/s00253-012-4085-1

Source DB:  PubMed          Journal:  Appl Microbiol Biotechnol        ISSN: 0175-7598            Impact factor:   4.813


  5 in total

1.  Cloning and Characterization of a Pyruvate Carboxylase Gene from Penicillium rubens and Overexpression of the Genein the Yeast Yarrowia lipolytica for Enhanced Citric Acid Production.

Authors:  Ge-Yi Fu; Yi Lu; Zhe Chi; Guang-Lei Liu; Shou-Feng Zhao; Hong Jiang; Zhen-Ming Chi
Journal:  Mar Biotechnol (NY)       Date:  2016-02       Impact factor: 3.619

2.  Identification and application of keto acids transporters in Yarrowia lipolytica.

Authors:  Hongwei Guo; Peiran Liu; Catherine Madzak; Guocheng Du; Jingwen Zhou; Jian Chen
Journal:  Sci Rep       Date:  2015-01-30       Impact factor: 4.379

3.  Irradiation of Yarrowia lipolytica NRRL YB-567 creating novel strains with enhanced ammonia and oil production on protein and carbohydrate substrates.

Authors:  Mitch R Lindquist; Juan Carlos López-Núñez; Marjorie A Jones; Elby J Cox; Rebecca J Pinkelman; Sookie S Bang; Bryan R Moser; Michael A Jackson; Loren B Iten; Cletus P Kurtzman; Kenneth M Bischoff; Siqing Liu; Nasib Qureshi; Kenneth Tasaki; Joseph O Rich; Michael A Cotta; Badal C Saha; Stephen R Hughes
Journal:  Appl Microbiol Biotechnol       Date:  2015-08-15       Impact factor: 4.813

4.  Functional overexpression of genes involved in erythritol synthesis in the yeast Yarrowia lipolytica.

Authors:  Aleksandra M Mirończuk; Anna Biegalska; Adam Dobrowolski
Journal:  Biotechnol Biofuels       Date:  2017-03-24       Impact factor: 6.040

5.  Optimization of Yarrowia lipolytica-based consolidated biocatalyst through synthetic biology approach: transcription units and signal peptides shuffling.

Authors:  Ewelina Celińska; Monika Borkowska; Paulina Korpys-Woźniak; Monika Kubiak; Jean-Marc Nicaud; Piotr Kubiak; Maria Gorczyca; Wojciech Białas
Journal:  Appl Microbiol Biotechnol       Date:  2020-05-02       Impact factor: 4.813

  5 in total

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