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PMID: 3947072 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Purification and partial sequence of the Mr 10,000 phosphoprotein from spinach thylakoids.

Archives of biochemistry and biophysics ·Vol. 244 ·No. 1 ·1986-01-00 ·Pages 94-101

Farchaus J, Dilley RA

Abstract

The Mr 10,000 phosphoprotein was purified from photosystem II particles by solubilization of the particles in 5% (w/v) dodecyl dimethylamine oxide, centrifugation in 10% (w/v) sucrose, and three chromatography steps. The purified phosphoprotein showed a unique NH2 terminus indicating a highly purified polypeptide. The amino acid sequence for the first nine residues is NH2-Ala-Thr-Gln-Thr-Val-Glu-Ser-Ser-Ser . . . COOH. The amino acid composition was determined and could also be used to help distinguish the polypeptide from other known thylakoid proteins. The sequence and composition data indicated that the Mr 10,000 phosphoprotein is neither the hydrophobic 8-kDa subunit of the energy coupling complex nor cytochrome b-559, but rather a unique, as yet unidentified, polypeptide associated with photosystem II.

MeSH Terms
Amino Acid Sequence Amino Acids/analysis Autoradiography Chloroplasts/analysis Electrophoresis, Polyacrylamide Gel Light Molecular Weight Phosphoproteins/isolation & purification Phosphorylation Plant Proteins/isolation & purification
Chemicals
Amino Acids Phosphoproteins Plant Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Farchaus J
Dilley R A
Article Info
Journal
Archives of biochemistry and biophysics
Abbr.
Arch Biochem Biophys
ISSN
0003-9861
Published
1986-01-00
Pages
94-101
Language
English
Region
United States
NLM ID
0372430
Subset
IM
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