Selective Protein Extraction from Chlorobium tepidum Chlorosomes Using Detergents. Evidence That CsmA Forms Multimers and Binds Bacteriochlorophyll a

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Selective Protein Extraction from Chlorobium tepidum Chlorosomes Using Detergents. Evidence That CsmA Forms Multimers and Binds Bacteriochlorophyll a. / Bryant, Donald A; Vassilieva, Elena V; Frigaard, Niels-Ulrik; Li, Hui.

In: Biochemistry, Vol. 41, No. 48, 2002, p. 14403-14411.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Bryant, DA, Vassilieva, EV, Frigaard, N-U & Li, H 2002, 'Selective Protein Extraction from Chlorobium tepidum Chlorosomes Using Detergents. Evidence That CsmA Forms Multimers and Binds Bacteriochlorophyll a', Biochemistry, vol. 41, no. 48, pp. 14403-14411. https://doi.org/10.1021/bi026599s

APA

Bryant, D. A., Vassilieva, E. V., Frigaard, N-U., & Li, H. (2002). Selective Protein Extraction from Chlorobium tepidum Chlorosomes Using Detergents. Evidence That CsmA Forms Multimers and Binds Bacteriochlorophyll a. Biochemistry, 41(48), 14403-14411. https://doi.org/10.1021/bi026599s

Vancouver

Bryant DA, Vassilieva EV, Frigaard N-U, Li H. Selective Protein Extraction from Chlorobium tepidum Chlorosomes Using Detergents. Evidence That CsmA Forms Multimers and Binds Bacteriochlorophyll a. Biochemistry. 2002;41(48):14403-14411. https://doi.org/10.1021/bi026599s

Author

Bryant, Donald A ; Vassilieva, Elena V ; Frigaard, Niels-Ulrik ; Li, Hui. / Selective Protein Extraction from Chlorobium tepidum Chlorosomes Using Detergents. Evidence That CsmA Forms Multimers and Binds Bacteriochlorophyll a. In: Biochemistry. 2002 ; Vol. 41, No. 48. pp. 14403-14411.

Bibtex

@article{0a20d0e0962611de8bc9000ea68e967b,
title = "Selective Protein Extraction from Chlorobium tepidum Chlorosomes Using Detergents. Evidence That CsmA Forms Multimers and Binds Bacteriochlorophyll a",
abstract = "Chlorosomes of the photosynthetic green sulfur bacterium Chlorobium tepidum consist of bacteriochlorophyll (BChl) c aggregates that are surrounded by a lipid-protein monolayer envelope that contains ten different proteins. Chlorosomes also contain a small amount of BChl a, but the organization and location of this BChl a are not yet clearly understood. Chlorosomes were treated with sodium dodecyl sulfate (SDS), Lubrol PX, or Triton X-100, separately or in combination with 1-hexanol, and the extracted components were separated from the residual chlorosomes by ultrafiltration on centrifugal filters. When chlorosomes were treated with low concentrations of SDS, all proteins except CsmA were extracted. However, this treatment did not significantly alter the size and shape of the chlorosomes, did not extract the BChl a, and caused only minor changes in the absorption spectrum of the chlorosomes. Cross-linking studies with SDS-treated chlorosomes revealed the presence of multimers of the major chlorosome protein, CsmA, up to homooctamers. Extraction of chlorosomes with SDS and 1-hexanol solubilized all ten chlorosome envelope proteins as well as BChl a. Although the size and shape of these extracted chlorosomes did not initially differ significantly from untreated chlorosomes, the extracted chlorosomes gradually disintegrated, and rod-shaped BChl c aggregates were sometimes observed. These results strongly suggest that CsmA binds the BChl a in Chlorobium-type chlorosomes and further indicate that none of the nine other chlorosome envelope proteins are absolutely required for maintaining the shape and integrity of chlorosomes. Quantitative estimates suggest that chlorosomes contain approximately equimolar amounts of CsmA and BChl a and that roughly one-third of the surface of the chlorosome is covered by CsmA.",
author = "Bryant, {Donald A} and Vassilieva, {Elena V} and Niels-Ulrik Frigaard and Hui Li",
note = "Keywords: Bacterial Proteins; Bacteriochlorophyll A; Biopolymers; Buffers; Chlorobi; Cross-Linking Reagents; Detergents; Hexanols; Octoxynol; Polyethylene Glycols; Protein Binding; Sodium Dodecyl Sulfate; Tromethamine",
year = "2002",
doi = "10.1021/bi026599s",
language = "English",
volume = "41",
pages = "14403--14411",
journal = "Biochemistry",
issn = "0006-2960",
publisher = "American Chemical Society",
number = "48",

}

RIS

TY - JOUR

T1 - Selective Protein Extraction from Chlorobium tepidum Chlorosomes Using Detergents. Evidence That CsmA Forms Multimers and Binds Bacteriochlorophyll a

AU - Bryant, Donald A

AU - Vassilieva, Elena V

AU - Frigaard, Niels-Ulrik

AU - Li, Hui

N1 - Keywords: Bacterial Proteins; Bacteriochlorophyll A; Biopolymers; Buffers; Chlorobi; Cross-Linking Reagents; Detergents; Hexanols; Octoxynol; Polyethylene Glycols; Protein Binding; Sodium Dodecyl Sulfate; Tromethamine

PY - 2002

Y1 - 2002

N2 - Chlorosomes of the photosynthetic green sulfur bacterium Chlorobium tepidum consist of bacteriochlorophyll (BChl) c aggregates that are surrounded by a lipid-protein monolayer envelope that contains ten different proteins. Chlorosomes also contain a small amount of BChl a, but the organization and location of this BChl a are not yet clearly understood. Chlorosomes were treated with sodium dodecyl sulfate (SDS), Lubrol PX, or Triton X-100, separately or in combination with 1-hexanol, and the extracted components were separated from the residual chlorosomes by ultrafiltration on centrifugal filters. When chlorosomes were treated with low concentrations of SDS, all proteins except CsmA were extracted. However, this treatment did not significantly alter the size and shape of the chlorosomes, did not extract the BChl a, and caused only minor changes in the absorption spectrum of the chlorosomes. Cross-linking studies with SDS-treated chlorosomes revealed the presence of multimers of the major chlorosome protein, CsmA, up to homooctamers. Extraction of chlorosomes with SDS and 1-hexanol solubilized all ten chlorosome envelope proteins as well as BChl a. Although the size and shape of these extracted chlorosomes did not initially differ significantly from untreated chlorosomes, the extracted chlorosomes gradually disintegrated, and rod-shaped BChl c aggregates were sometimes observed. These results strongly suggest that CsmA binds the BChl a in Chlorobium-type chlorosomes and further indicate that none of the nine other chlorosome envelope proteins are absolutely required for maintaining the shape and integrity of chlorosomes. Quantitative estimates suggest that chlorosomes contain approximately equimolar amounts of CsmA and BChl a and that roughly one-third of the surface of the chlorosome is covered by CsmA.

AB - Chlorosomes of the photosynthetic green sulfur bacterium Chlorobium tepidum consist of bacteriochlorophyll (BChl) c aggregates that are surrounded by a lipid-protein monolayer envelope that contains ten different proteins. Chlorosomes also contain a small amount of BChl a, but the organization and location of this BChl a are not yet clearly understood. Chlorosomes were treated with sodium dodecyl sulfate (SDS), Lubrol PX, or Triton X-100, separately or in combination with 1-hexanol, and the extracted components were separated from the residual chlorosomes by ultrafiltration on centrifugal filters. When chlorosomes were treated with low concentrations of SDS, all proteins except CsmA were extracted. However, this treatment did not significantly alter the size and shape of the chlorosomes, did not extract the BChl a, and caused only minor changes in the absorption spectrum of the chlorosomes. Cross-linking studies with SDS-treated chlorosomes revealed the presence of multimers of the major chlorosome protein, CsmA, up to homooctamers. Extraction of chlorosomes with SDS and 1-hexanol solubilized all ten chlorosome envelope proteins as well as BChl a. Although the size and shape of these extracted chlorosomes did not initially differ significantly from untreated chlorosomes, the extracted chlorosomes gradually disintegrated, and rod-shaped BChl c aggregates were sometimes observed. These results strongly suggest that CsmA binds the BChl a in Chlorobium-type chlorosomes and further indicate that none of the nine other chlorosome envelope proteins are absolutely required for maintaining the shape and integrity of chlorosomes. Quantitative estimates suggest that chlorosomes contain approximately equimolar amounts of CsmA and BChl a and that roughly one-third of the surface of the chlorosome is covered by CsmA.

U2 - 10.1021/bi026599s

DO - 10.1021/bi026599s

M3 - Journal article

C2 - 12450407

VL - 41

SP - 14403

EP - 14411

JO - Biochemistry

JF - Biochemistry

SN - 0006-2960

IS - 48

ER -

ID: 14095589