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The proteinase yscB inhibitor (PBI2) gene of yeast and studies on the function of its protein product

dc.contributor.authorSchu, Peter
dc.contributor.authorSuárez Rendueles, María Paz 
dc.contributor.authorWolf, Dieter H.
dc.date.accessioned2014-12-01T12:00:52Z
dc.date.available2014-12-01T12:00:52Z
dc.date.issued1991
dc.identifier.citationEuropean Journal of Biochemistry, 197(1), p. 1-7 (1991); doi:10.1111/j.1432-1033.1991.tb15874.xen
dc.identifier.issn0014-5793
dc.identifier.issn1873-3468
dc.identifier.urihttp://hdl.handle.net/10651/28930
dc.description.abstractThe gene for proteinase yscB inhibitor I2B (PBI2) from Saccharomyces cerevisiae was isolated by oligonucleotide screening of a genomic DNA library, and was sequenced. The gene codes for a single protein of 75 amino acids. In contrast to the published amino acid sequence [Maier, K., Muller, H., Tesch, R., Trolp, T., Witt, I. & Holzer, H. (1979) J. Biol. Chem. 254, 12555-12561] the DNA sequence revealed a valine instead of a leucine at position 33 (32 of the mature protein). Therefore the primary sequences of the isoinhibitors I2B of S. cerevisiae and I1B of Saccharomyces carlsbergensis differ only at position 34 (glutamic acid/lysine). The open reading frame of PBI2 was replaced in vitro by the URA3 gene and a I2B null mutant of S. cerevisiae was constructed by gene replacement. The mutation resulted in an elevation of the protein degradation rate by 50% when grown under nutritional stress compared to the isogenic wild type. Growth and viability of the cells was not significantly affected by the absence of I2Ben
dc.description.sponsorshipTrabajo financiado con fondos de Deutsche Forschungs~emein.sc.haft (Wo 210/8 - 1) y Fond.s der Chemisehen Industrie
dc.format.extent7 p.spa
dc.language.isoengspa
dc.publisherElsevier
dc.relation.ispartofEuropean Journal of Biochemistry, 197(1)en
dc.rights© Wiley
dc.titleThe proteinase yscB inhibitor (PBI2) gene of yeast and studies on the function of its protein producten
dc.typejournal article
dc.identifier.doi10.1111/j.1432-1033.1991.tb15874.x
dc.relation.publisherversionhttp://dx.doi.org/10.1111/j.1432-1033.1991.tb15874.x


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