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Proteomic analysis of chlorosome‐depleted membranes of the green sulfur bacterium Chlorobium tepidum
Author(s) -
Aivaliotis Michalis,
Haase Winfried,
Karas Michael,
Tsiotis Georgios
Publication year - 2006
Publication title -
proteomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.26
H-Index - 167
eISSN - 1615-9861
pISSN - 1615-9853
DOI - 10.1002/pmic.200402030
Subject(s) - chlorosome , triton x 100 , membrane , chemistry , membrane protein , bacterial outer membrane , proteome , chromatography , chaps , bacteria , gel electrophoresis , biochemistry , ftsz , biology , escherichia coli , pulmonary surfactant , bacteriochlorophyll , photosynthesis , gene , genetics
Abstract Green sulfur bacteria are obligate anaerobic phototrophs, which in addition to outer and plasma membranes contain chlorosomes. The analysis of the membrane proteome of Chlorobium tepidum from chlorosome‐depleted membranes is described in this study. The membranes were purified by sucrose density centrifugation and characterized by 1‐DE and 2‐DE coupled with MS, absorption spectroscopy, and electron microscopy. 1‐DE and 2‐DE were employed to analyze the membrane proteins and to characterize the capabilities of the methods. Solubilization of the membrane proteins prior to 2‐DE was improved by using a series of zwitterionic detergents. Based on the resolved spots after 2‐DE, the combination of amidosulfobetaine 14 with Triton X‐100 is more efficient than the combination of CHAPS, N ‐decyl‐ N,N ‐dimethyl‐3‐ammonio‐1‐propane sulfonate, and Triton X‐100. From the application of 1‐DE and 2‐DE, 167 and 202 unique proteins were identified, respectively, using PMF by MALDI‐TOF MS. Both methods resulted in the detection of 291 different proteins of which only 88 were predicted membrane proteins, indicating the limitation of membrane protein detection after separation with electrophoresis methods. In addition, 53 of these proteins were identified as outer membrane proteins.