Literature DB >> 19187186

Use of novel selenomethionine-resistant yeast to produce selenomethionyl protein suitable for structural analysis.

Toshihiko Kitajima1, Emi Yagi, Tomomi Kubota, Yasunori Chiba, Satoshi Nishikawa, Yoshifumi Jigami.   

Abstract

Yeast is widely used to determine the tertiary structure of eukaryotic proteins, because of its ability to undergo post-translational modifications such as glycosylation. A mutant lacking S-adenosylmethionine synthesis has been reported as a suitable host for producing selenomethionine derivatives, which can help solve phase problems in protein crystallography. However, the mutant required external addition of S-adenosylmethionine for cell proliferation. Here, a selenomethionine-resistant Pichia pastoris mutant that showed S-adenosylmethionine autotrophy was isolated. Human lysozyme expressed by the mutant under the control of constitutive promoter contained selenomethionine at 65% occupancy, sufficient for use as a selenomethionine derivative for single-wavelength anomalous dispersion phasing.

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Year:  2009        PMID: 19187186     DOI: 10.1111/j.1567-1364.2009.00484.x

Source DB:  PubMed          Journal:  FEMS Yeast Res        ISSN: 1567-1356            Impact factor:   2.796


  2 in total

1.  Mutation of high-affinity methionine permease contributes to selenomethionyl protein production in Saccharomyces cerevisiae.

Authors:  Toshihiko Kitajima; Yasunori Chiba; Yoshifumi Jigami
Journal:  Appl Environ Microbiol       Date:  2010-08-06       Impact factor: 4.792

2.  A practical method for efficient and optimal production of Seleno-methionine-labeled recombinant protein complexes in the insect cells.

Authors:  Sabine Wenzel; Tsuyoshi Imasaki; Yuichiro Takagi
Journal:  Protein Sci       Date:  2019-02-04       Impact factor: 6.725

  2 in total

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