4.7 Article

Change of Carbon Source Causes Dramatic Effects in the Phospho-Proteome of the Archaeon Sulfolobus solfataricus

Journal

JOURNAL OF PROTEOME RESEARCH
Volume 11, Issue 10, Pages 4823-4833

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/pr300190k

Keywords

Archaea; Sulfolobus solfataricus; Phospho-proteomics; Protein phosphorylation; PAcIFIC; Central carbohydrate metabolism

Funding

  1. BMBF [0315004A, 0315004C]
  2. BBSRC [BB/F003420/1]
  3. Dutch Science Organization (NWO)
  4. Max Planck Society
  5. EPSRC [EP/E036252/1]
  6. Biotechnology and Biological Sciences Research Council [BB/F003420/1] Funding Source: researchfish
  7. Engineering and Physical Sciences Research Council [EP/E036252/1] Funding Source: researchfish
  8. BBSRC [BB/F003420/1] Funding Source: UKRI
  9. EPSRC [EP/E036252/1] Funding Source: UKRI

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Protein phosphorylation is known to occur in Archaea. However, knowledge of phosphorylation in the third domain of life is rather scarce. Homology-based searches of archaeal genome sequences reveals the absence of two-component systems in crenarchaeal genomes but the presence of eukaryotic-like protein kinases and protein phosphatases. Here, the influence of the offered carbon source (glucose versus tryptone) on the phospho-proteome of Sulfolobus solfataricus P2 was studied by precursor acquisition independent from ion count (PAcIFIC). In comparison to previous phospho-proteome studies, a high number of phosphorylation sites (1318) located on 690 phospho-peptides from 540 unique phospho-proteins were detected, thus increasing the number of currently known archaeal phospho-proteins from 80 to 621. Furthermore, a 25.8/20.6/53.6 Ser/Thr/Tyr percentage ratio with an unexpectedly high predominance of tyrosine phosphorylation was detected. Phospho-proteins in functional classes (21 out of 26 arCOGs) were identified, suggesting an important regulatory role in S. solfataricus. Focusing on the central carbohydrate metabolism in response to the offered carbon source, significant changes were observed. The observed complex phosphorylation pattern hints at an important physiological function of protein phosphorylation in control of the central carbohydrate metabolism, which might particularly operate in channeling carbon flux into the respective metabolic pathways.

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