Quantitative proteomic analysis of metabolic regulation by copper ions in Methylococcus capsulatus (Bath)

被引:69
作者
Kao, WC
Chen, YR
Yi, EC
Lee, H
Tian, Q
Wu, KM
Tsai, SF
Yu, SSF
Chen, YJ
Aebersold, R
Chan, SI
机构
[1] Acad Sinica, Inst Chem, Taipei 115, Taiwan
[2] Natl Taiwan Univ, Dept Chem, Taipei 106, Taiwan
[3] Inst Syst Biol, Seattle, WA 98103 USA
[4] Natl Yang Ming Univ, Inst Genet & Genome Res Ctr, Taipei 112, Taiwan
[5] Natl Hlth Res Inst, Div Mol & Genom Med, Taipei 115, Taiwan
关键词
D O I
10.1074/jbc.M408013200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Copper ions switch the oxidation of methane by soluble methane monooxygenase to particulate methane monooxygenase in Methylococcus capsulatus ( Bath). Toward understanding the change in cellular metabolism related to this transcriptional and metabolic switch, we have undertaken genomic sequencing and quantitative comparative analysis of the proteome in M. capsulatus ( Bath) grown under different copper-to-biomass ratios by cleavable isotope-coded affinity tag technology. Of the 682 proteins identified, the expressions of 60 proteins were stimulated by at least 2-fold by copper ions; 68 proteins were down-regulated by 2-fold or more. The 60 proteins overexpressed included the methane and carbohydrate metabolic enzymes, while the 68 proteins suppressed were mainly responsible for cellular signaling processes, indicating a role of copper ions in the expression of the genes associated with the metabolism of the organism downstream of methane oxidation. The study has also provided a complete
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页码:51554 / 51560
页数:7
相关论文
共 36 条
[21]   EXPERT SYSTEM FOR PREDICTING PROTEIN LOCALIZATION SITES IN GRAM-NEGATIVE BACTERIA [J].
NAKAI, K ;
KANEHISA, M .
PROTEINS-STRUCTURE FUNCTION AND GENETICS, 1991, 11 (02) :95-110
[22]   A statistical model for identifying proteins by tandem mass spectrometry [J].
Nesvizhskii, AI ;
Keller, A ;
Kolker, E ;
Aebersold, R .
ANALYTICAL CHEMISTRY, 2003, 75 (17) :4646-4658
[23]   PREDICTION OF TRANSMEMBRANE SEGMENTS IN PROTEINS UTILIZING MULTIPLE SEQUENCE ALIGNMENTS [J].
PERSSON, B ;
ARGOS, P .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 237 (02) :182-192
[24]   Generation of formate by the formyltransferase/hydrolase complex (Fhc) from Methylobacterium extorquens AM1 [J].
Pomper, BK ;
Saurel, O ;
Milon, A ;
Vorholt, JA .
FEBS LETTERS, 2002, 523 (1-3) :133-137
[25]   EVOLUTIONARY ASPECTS OF AUTOTROPHY [J].
QUAYLE, JR ;
FERENCI, T .
MICROBIOLOGICAL REVIEWS, 1978, 42 (02) :251-273
[26]   EMBOSS: The European molecular biology open software suite [J].
Rice, P ;
Longden, I ;
Bleasby, A .
TRENDS IN GENETICS, 2000, 16 (06) :276-277
[27]   Role of multiple gene copies in particulate methane monooxygenase activity in the methane-oxidizing bacterium Methylococcus capsulatus Bath [J].
Stolyar, S ;
Costello, AM ;
Peeples, TL ;
Lidstrom, ME .
MICROBIOLOGY-UK, 1999, 145 :1235-1244
[28]   Crystal structure at 2.6-angstrom resolution of human macrophage migration inhibitory factor [J].
Sun, HW ;
Bernhagen, J ;
Bucala, R ;
Lolis, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (11) :5191-5196
[29]   NUCLEOTIDE-SEQUENCE AND CLONING IN BACILLUS-SUBTILIS OF THE BACILLUS-STEAROTHERMOPHILUS PLEIOTROPIC REGULATORY GENE DEGT [J].
TAKAGI, M ;
TAKADA, H ;
IMANAKA, T .
JOURNAL OF BACTERIOLOGY, 1990, 172 (01) :411-418
[30]   The COG database: new developments in phylogenetic classification of proteins from complete genomes [J].
Tatusov, RL ;
Natale, DA ;
Garkavtsev, IV ;
Tatusova, TA ;
Shankavaram, UT ;
Rao, BS ;
Kiryutin, B ;
Galperin, MY ;
Fedorova, ND ;
Koonin, EV .
NUCLEIC ACIDS RESEARCH, 2001, 29 (01) :22-28