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Details

Autor(en) / Beteiligte
Titel
Enhancement of Sphingolipid Synthesis Improves Osmotic Tolerance of Saccharomyces cerevisiae
Ist Teil von
  • Applied and environmental microbiology, 2020-04, Vol.86 (8), p.1
Ort / Verlag
United States: American Society for Microbiology
Erscheinungsjahr
2020
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • To enhance the growth performance of under osmotic stress, mutant XCG001, which tolerates up to 1.5 M NaCl, was isolated through adaptive laboratory evolution (ALE). Comparisons of the transcriptome data of mutant XCG001 and the wild-type strain identified as being associated with osmotic tolerance. In the overexpression strain (XCG010), the contents of inositol phosphorylceramide (IPC; t18:0/26:0), mannosylinositol phosphorylceramide [MIPC; t18:0/22:0(2OH)], MIPC (d18:0/22:0), MIPC (d20:0/24:0), mannosyldiinositol phosphorylceramide [M(IP) C; d20:0/26:0], M(IP) C [t18:0/26:0(2OH)], and M(IP) C [d20:0/26:0(2OH)] increased by 88.3 times, 167 times, 63.3 times, 23.9 times, 27.9 times, 114 times, and 208 times at 1.0 M NaCl, respectively, compared with the corresponding values of the control strain XCG002. As a result, the membrane integrity, cell growth, and cell survival rate of strain XCG010 increased by 24.4% ± 1.0%, 21.9% ± 1.5%, and 22.1% ± 1.1% at 1.0 M NaCl, respectively, compared with the corresponding values of the control strain XCG002 (wild-type strain with a control plasmid). These findings provided a novel strategy for engineering complex sphingolipids to enhance osmotic tolerance. This study demonstrated a novel strategy for the manipulation of membrane complex sphingolipids to enhance tolerance to osmotic stress. Elo2, a sphingolipid acyl chain elongase, was related to osmotic tolerance through transcriptome analysis of the wild-type strain and an osmosis-tolerant strain generated from ALE. Overexpression of increased the content of complex sphingolipid with longer acyl chain; thus, membrane integrity and osmotic tolerance improved.
Sprache
Englisch
Identifikatoren
ISSN: 0099-2240
eISSN: 1098-5336
DOI: 10.1128/aem.02911-19
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7117927

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