Literature DB >> 6093709

Triton X-114 phase fractionation of membrane proteins of the cyanobacterium Anacystis nidulans R2.

T M Bricker, L A Sherman.   

Abstract

The thylakoid polypeptides of the cyanobacterium Anacystis nidulans R2 were analyzed by Triton X-114 phase fractionation [C. Bordier (1981) J. Biol. Chem. 256, 1604-1607, as adapted for photosynthetic membranes by T.M. Bricker and L.A. Sherman (1982) FEBS Lett. 149, 197-202]. In this procedure, polypeptides with extensive hydrophobic regions (i.e., intrinsic proteins) form mixed micelles with Triton X-114, and are separated from extrinsic proteins by temperature-mediated precipitation of the mixed Triton X-114-intrinsic protein micelles. The polypeptide pattern after phase fractionation was highly complementary, with 62 of the observed 110 polypeptide components partitioning into the Triton X-114-enriched fraction. Identified polypeptides fractionating into the Triton X-114 phase included the apoproteins for Photosystems I and II, cytochromes f and b6, and the herbicide-binding protein. Identified polypeptides fractioning into the Triton X-114-depleted (aqueous) phase included the large and small subunits of RuBp carboxylase, cytochromes c550 and c554, and ferredoxin. Enzymatic radioiodination of the photosynthetic membranes followed by Triton X-114 phase fractionation allowed direct identification of intrinsic polypeptide components which possess surface-exposed regions susceptible to radioiodination. The most prominent of these polypeptides was a 34-kDa component which was associated with photosystem II. This phase partitioning procedure has been particularly helpful in the clarification of the identity of the membrane-associated cytochromes, and of photosystem II components. When coupled with surface-probing techniques, this procedure is very useful in identifying intrinsic proteins which possess surface-exposed domains. Phase fractionation, in conjunction with the isolation of specific membrane components and complexes, has allowed the identification of many of the important intrinsic thylakoid membrane proteins of A. nidulans R2.

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Year:  1984        PMID: 6093709     DOI: 10.1016/0003-9861(84)90269-8

Source DB:  PubMed          Journal:  Arch Biochem Biophys        ISSN: 0003-9861            Impact factor:   4.013


  8 in total

Review 1.  Photosensory behavior in procaryotes.

Authors:  D P Häder
Journal:  Microbiol Rev       Date:  1987-03

2.  MapA, an iron-regulated, cytoplasmic membrane protein in the cyanobacterium Synechococcus sp. strain PCC7942.

Authors:  R Webb; T Troyan; D Sherman; L A Sherman
Journal:  J Bacteriol       Date:  1994-08       Impact factor: 3.490

3.  Effect of Nitrogen Starvation on Polypeptide Composition, Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase, and Thylakoid Carotenoprotein Content of Synechocystis sp. Strain PCC6308.

Authors:  C S Duke; M M Allen
Journal:  Plant Physiol       Date:  1990-10       Impact factor: 8.340

4.  Isolation and Characterization of a Carotenoid-Associated Thylakoid Protein from the Cyanobacterium Anacystis nidulans R2.

Authors:  K Masamoto; H C Riethman; L A Sherman
Journal:  Plant Physiol       Date:  1987-07       Impact factor: 8.340

5.  Characterization of phycobilisome glycoproteins in the cyanobacterium Anacystis nidulans R2.

Authors:  H C Riethman; T P Mawhinney; L A Sherman
Journal:  J Bacteriol       Date:  1988-06       Impact factor: 3.490

6.  Very low osmotic water permeability and membrane fluidity in isolated toad bladder granules.

Authors:  A S Verkman; S K Masur
Journal:  J Membr Biol       Date:  1988-09       Impact factor: 1.843

7.  Organization of pigment proteins in the photosystem II complex of the cyanobacterium Anacystis nidulans R2.

Authors:  H B Pakrasi; H C Riethman; L A Sherman
Journal:  Proc Natl Acad Sci U S A       Date:  1985-10       Impact factor: 11.205

8.  N-Terminal Lipid Modification Is Required for the Stable Accumulation of CyanoQ in Synechocystis sp. PCC 6803.

Authors:  Andrea D Juneau; Laurie K Frankel; Terry M Bricker; Johnna L Roose
Journal:  PLoS One       Date:  2016-09-22       Impact factor: 3.240

  8 in total

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