4.7 Article

Investigating the Role of Respiration in Plant Salinity Tolerance by Analyzing Mitochondrial Proteomes from Wheat and a Salinity-Tolerant Amphiploid (Wheat x Lophopyrum elongatum)

期刊

JOURNAL OF PROTEOME RESEARCH
卷 12, 期 11, 页码 4807-4829

出版社

AMER CHEMICAL SOC
DOI: 10.1021/pr400504a

关键词

mitochondria; respiration; salinity; wheat; MnSOD; proteomics; 2D-DIGE; mass spectrometry; de novo sequencing; beta-cyanoalanine synthase

资金

  1. GRDC PhD scholarship [GRS163]
  2. Australian Research Council (ARC) [CE0561495, LP120200102]
  3. ARC [FT110100242]
  4. Australian Research Council [LP120200102] Funding Source: Australian Research Council

向作者/读者索取更多资源

The effect of salinity on mitochondrial properties was investigated by comparing the reference wheat variety Chinese Spring (CS) to a salt-tolerant amphiploid (AMP). The octoploid AMP genotype was previously generated by combining hexaploid bread wheat (CS) with the diploid wild wheatgrass adapted to salt marshes, Lophopyrum elongatum. Here we used a combination of physiological, biochemical, and proteomic analyses to explore the mitochondrial and respiratory response to salinity in these two genotypes. The AMP showed greater growth tolerance to salinity treatments and altered respiration rate in both roots and shoots. A proteomic workflow of 2D-DIGE and MALDI TOF/TOF Triticum Lophopyrum mass spectrometry was used to compare the protein composition of isolated mitochondrial samples from roots and shoots of both genotypes, following control or salt treatment. A large set of mitochondrial proteins were identified as responsive to salinity in both genotypes, notably enzymes involved in detoxification of reactive oxygen species. Genotypic differences in mitochondrial composition were also identified, with AMP exhibiting a higher abundance of manganese superoxide dismutase, serine hydroxymethyltransferase, aconitase, malate dehydrogenase, and beta-cyanoalanine synthase compared to CS. We present peptide fragmentation spectra derived from some of these AMP-specific protein spots, which could serve as biomarkers to track superior protein variants.

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