Strategic proteome analysis of Candida magnoliae with an unsequenced genome

被引:19
作者
Kim, HJ
Lee, DY
Lee, DH
Park, YC
Kweon, DH
Ryu, YW
Seo, JH [1 ]
机构
[1] Seoul Natl Univ, Sch Agr Biotechnol, Seoul 151742, South Korea
[2] Seoul Natl Univ, Ctr Agr Biomat, Seoul 151742, South Korea
[3] Andong Natl Univ, Sch Bioresource Sci, Kyungbuk, South Korea
[4] Ajou Univ, Dept Mol Sci & Technol, Suwon, South Korea
关键词
Candida magnoliae; expressed sequence tag; mass spectrometry; orthologous protein; two-dimensional gel electrophoresis;
D O I
10.1002/pmic.200400966
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Erythritol is a noncariogenic, low calorie sweetener. It is safe for people with diabetes and obese people. Candida magnoliae is an industrially important organism because of its ability to produce erythritol as a major product. The genome of C. magnoliae has not been sequenced yet, limiting the available proteome database. Therefore, systematic approaches were employed to construct the proteome map of C. magnoliae. Proteomic analysis with systematic approaches is based on two-dimensional electrophoresis, matrix-assisted laser desorption ionization time of flight mass spectrometry (MALDI-TOF MS), tandem mass spectrometry (MS/MS) and database interrogation. First, 24 spots were analyzed using peptide mass fingerprinting along with MALDI-TOF MS with high mass accuracy. Only four spots were reliably identified as carbonyl reductase and its isoforms. The reason for low sequence coverage seemed to be that these identification strategies were based on the presence of the protein database obtained from the publicly accessible genome database and the availability of cross-species protein identification. MS/MS (MS/MS ion search and de novo sequencing) in combination with similarity searches allowed successful identification of 39 spots. Several proteins including transaldolase identified by MS/MS ion searches were further confirmed by partial sequences from the expressed sequence tag database. In this study, 51 protein spots were analyzed and then potentially identified. The identified proteins were involved in glycolysis, stress response, other essential metabolisms and cell structures.
引用
收藏
页码:3588 / 3599
页数:12
相关论文
共 25 条
[11]   Fumarate-mediated inhibition of erythrose reductase, a key enzyme for erythritol production by Torula corallina [J].
Lee, JK ;
Koo, BS ;
Kim, SY .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2002, 68 (09) :4534-4538
[12]  
Lester PJ, 2002, PROTEOMICS, V2, P1392, DOI 10.1002/1615-9861(200210)2:10<1392::AID-PROT1392>3.0.CO
[13]  
2-L
[14]   Expanding the organismal scope of proteomics: Cross-species protein identification by mass spectrometry and its implications [J].
Liska, AJ ;
Shevchenko, A .
PROTEOMICS, 2003, 3 (01) :19-28
[15]   Getting more from less - Algorithms for rapid protein identification with multiple short peptide sequences [J].
Mackey, AJ ;
Haystead, TAJ ;
Pearson, WR .
MOLECULAR & CELLULAR PROTEOMICS, 2002, 1 (02) :139-147
[16]   Using orthologous and paralogous proteins to identify specificity-determining residues in bacterial transcription factors [J].
Mirny, LA ;
Gelfand, MS .
JOURNAL OF MOLECULAR BIOLOGY, 2002, 321 (01) :7-20
[17]   METABOLISM AND DISPOSITION OF ERYTHRITOL AFTER ORAL-ADMINISTRATION TO RATS [J].
NODA, K ;
OKU, T .
JOURNAL OF NUTRITION, 1992, 122 (06) :1266-1272
[18]   ERYTHRITOL, A NEW RAW-MATERIAL FOR FOOD AND NONFOOD APPLICATIONS [J].
ROPER, H ;
GOOSSENS, J .
STARCH-STARKE, 1993, 45 (11) :400-405
[19]   Charting the proteomes of organisms with unsequenced genomes by MALDI-quadrupole time of flight mass spectrometry and BLAST homology searching [J].
Shevchenko, A ;
Sunyaev, S ;
Loboda, A ;
Shevehenko, A ;
Bork, P ;
Ens, W ;
Standing, KG .
ANALYTICAL CHEMISTRY, 2001, 73 (09) :1917-1926
[20]   Linking genome and proteome by mass spectrometry: Large-scale identification of yeast proteins from two dimensional gels [J].
Shevchenko, A ;
Jensen, ON ;
Podtelejnikov, AV ;
Sagliocco, F ;
Wilm, M ;
Vorm, O ;
Mortensen, P ;
Shevchenko, A ;
Boucherie, H ;
Mann, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14440-14445