This Article Full Text (PDF) Other Versions of this Article: EC.00191-06v1 6/3/495    most recent Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Mühlenhoff, U. Articles by Stolz, J. Search for Related Content PubMed PubMed Citation Articles by Mühlenhoff, U. Articles by Stolz, J.

 Previous Article  |  Next Article 

Eukaryotic Cell doi:10.1128/EC.00191-06
Copyright (c) 2007, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.

The Fe/S assembly proteins Isa1 and Isa2 are required for the function but not for the de novo synthesis of the Fe/S clusters of biotin synthase in Saccharomyces cerevisiae

Institut für Zytobiologie und Zytopathologie; Philipps-Universität Marburg; Robert-Koch-Strasse 6, 35033 Marburg, Germany; Lehrstuhl für Zellbiologie und Pflanzenphysiologie; Universität Regensburg; Universitätsstrasse 31; 93040 Regensburg, Germany

^* To whom correspondence should be addressed. Email: juergen.stolz{at}biologie.uni-regensburg.de.

	Abstract

The yeast Saccharomyces cerevisiae is able to use some biotin precursors for biotin biosynthesis. Insertion of a sulfur atom into desthiobiotin, the final step in the biosynthetic pathway, is catalyzed by biotin synthase (Bio2). This mitochondrial protein contains two iron-sulfur (Fe/S) clusters that catalyze the reaction and are thought to act as a sulfur donor. To identify new components of biotin metabolism, we performed a genetic screen and found that Isa2, a mitochondrial protein involved in the formation of Fe/S clusters, is necessary for the conversion of desthiobiotin to biotin. Depletion of Isa2 or the related Isa1, however, did not prevent the de novo synthesis of any of the two Fe/S centers of Bio2. In contrast, Fe/S cluster assembly on Bio2 strongly depended on the Isu1/Isu2 proteins. Both isa mutants contained low levels of Bio2. This phenotype was also found in other mutants impaired in mitochondrial Fe/S protein assembly and in wild-type cells grown under iron-limitation. Low Bio2 levels, however, did not cause the inability of isa mutants to utilize desthiobiotin, since this defect was not cured by over-expression of BIO2. Thus, the Isa proteins are crucial for the in vivo function of biotin synthase but not for the de novo synthesis of its Fe/S clusters. Our data demonstrate that the Isa proteins are essential for the catalytic activity of Bio2 in vivo.

This article has been cited by other articles:

• Godman, J., Balk, J. (2008). Genome Analysis of Chlamydomonas reinhardtii Reveals The Existence of Multiple, Compartmentalized Iron-Sulfur Protein Assembly Machineries of Different Evolutionary Origins. Genetics 179: 59-68 [Abstract] [Full Text]