Literature DB >> 11469807

Cloning of Pichia pastoris Fet3: insights into the high affinity iron uptake system.

M P Paronetto1, R Miele, A Maugliani, M Borro, M C Bonaccorsi di Patti.   

Abstract

High-affinity iron uptake by yeast cells appears to require the presence of a complex formed on the plasma membrane by the multicopper oxidase Fet3 and the permease Ftr1 which work together to allow iron to enter safely inside the cell. The Pichia pastoris ferroxidase Fet3 has been cloned and it has been found to display high sequence similarity to other yeast multicopper oxidases, including all the predicted ligands for the catalytic copper atoms and for the iron substrate. P. pastoris appears to possess a high-affinity iron uptake system similar to that of S. cerevisiae, as far as regulation of expression is concerned. However, the P. pastoris high-affinity iron uptake system presents a K(m) value for iron almost ten times higher than that of S. cerevisiae, possibly to control iron fluxes over a wider range of concentrations of this metal, in order to avoid toxic iron overloading. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11469807     DOI: 10.1006/abbi.2001.2425

Source DB:  PubMed          Journal:  Arch Biochem Biophys        ISSN: 0003-9861            Impact factor:   4.013


  2 in total

1.  Secretion of two novel enzymes, manganese 9S-lipoxygenase and epoxy alcohol synthase, by the rice pathogen Magnaporthe salvinii.

Authors:  Anneli Wennman; Ernst H Oliw
Journal:  J Lipid Res       Date:  2012-12-11       Impact factor: 5.922

2.  Pichia pastoris Fep1 is a [2Fe-2S] protein with a Zn finger that displays an unusual oxygen-dependent role in cluster binding.

Authors:  Antimo Cutone; Barry D Howes; Adriana E Miele; Rossella Miele; Alessandra Giorgi; Andrea Battistoni; Giulietta Smulevich; Giovanni Musci; Maria Carmela Bonaccorsi di Patti
Journal:  Sci Rep       Date:  2016-08-22       Impact factor: 4.379

  2 in total

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