Literature DB >> 1767588

The use of proline as a nitrogen source causes hypersensitivity to, and allows more economical use of 5FOA in Saccharomyces cerevisiae.

J H McCusker1, R W Davis.   

Abstract

The use of proline as a nitrogen source causes hypersensitivity to 5-fluoro-orotic acid (5FOA) and allows up to 40-fold less of this drug to be used to select for the loss of URA3 function in Saccharomyces cerevisiae. 5FOA hypersensitivity is presumably due to the absence of nitrogen catabolite repression when proline is substituted for (NH4)2SO4 as a nitrogen source. There are two constraints to the use of the proline-5FOA combination: (1) S288c genetic background strains are hypersensitive to 5FOA when grown in proline as a nitrogen source but at least one other genetic background is resistant to low levels of 5FOA under these conditions. (2) The addition of some nutritional supplements confers phenotypic resistance to the 5FOA-proline combination.

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Year:  1991        PMID: 1767588     DOI: 10.1002/yea.320070608

Source DB:  PubMed          Journal:  Yeast        ISSN: 0749-503X            Impact factor:   3.239


  17 in total

1.  Accumulation of H/ACA snoRNPs depends on the integrity of the conserved central domain of the RNA-binding protein Nhp2p.

Authors:  A Henras; C Dez; J Noaillac-Depeyre; Y Henry; M Caizergues-Ferrer
Journal:  Nucleic Acids Res       Date:  2001-07-01       Impact factor: 16.971

2.  Morphogenesis, adhesive properties, and antifungal resistance depend on the Pmt6 protein mannosyltransferase in the fungal pathogen candida albicans.

Authors:  C Timpel; S Zink; S Strahl-Bolsinger; K Schröppel; J Ernst
Journal:  J Bacteriol       Date:  2000-06       Impact factor: 3.490

3.  Mitotic recombination and genetic changes in Saccharomyces cerevisiae during wine fermentation.

Authors:  S Puig; A Querol; E Barrio; J E Pérez-Ortín
Journal:  Appl Environ Microbiol       Date:  2000-05       Impact factor: 4.792

4.  Multicopy suppression screening of Saccharomyces cerevisiae Identifies the ubiquitination machinery as a main target for improving growth at low temperatures.

Authors:  Maria José Hernández-López; Sara García-Marqués; Francisca Randez-Gil; Jose Antonio Prieto
Journal:  Appl Environ Microbiol       Date:  2011-09-09       Impact factor: 4.792

5.  Propagation of the yeast prion-like [psi+] determinant is mediated by oligomerization of the SUP35-encoded polypeptide chain release factor.

Authors:  S V Paushkin; V V Kushnirov; V N Smirnov; M D Ter-Avanesyan
Journal:  EMBO J       Date:  1996-06-17       Impact factor: 11.598

6.  hNaf1 is required for accumulation of human box H/ACA snoRNPs, scaRNPs, and telomerase.

Authors:  Coralie Hoareau-Aveilla; Mattia Bonoli; Michele Caizergues-Ferrer; Yves Henry
Journal:  RNA       Date:  2006-04-06       Impact factor: 4.942

7.  Replacement of a metabolic pathway for large-scale production of lactic acid from engineered yeasts.

Authors:  D Porro; M M Bianchi; L Brambilla; R Menghini; D Bolzani; V Carrera; J Lievense; C L Liu; B M Ranzi; L Frontali; L Alberghina
Journal:  Appl Environ Microbiol       Date:  1999-09       Impact factor: 4.792

8.  Identification of SSF1, CNS1, and HCH1 as multicopy suppressors of a Saccharomyces cerevisiae Hsp90 loss-of-function mutation.

Authors:  D F Nathan; M H Vos; S Lindquist
Journal:  Proc Natl Acad Sci U S A       Date:  1999-02-16       Impact factor: 11.205

9.  L-proline as a nitrogen source increases the susceptibility of Saccharomyces cerevisiae S288c to fluconazole.

Authors:  C A Stella; R Costanzo; H I Burgos; D A Saenz; R D Venerus
Journal:  Folia Microbiol (Praha)       Date:  1998       Impact factor: 2.099

10.  Genetic interaction between the Ras-cAMP pathway and the Dis2s1/Glc7 protein phosphatase in Saccharomyces cerevisiae.

Authors:  A Matsuura; Y Anraku
Journal:  Mol Gen Genet       Date:  1994-02
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