Identification of a GDP-mannose pyrophosphorylase gene from Sulfolobus solfataricus

被引:6
|
作者
Sacchetti, S
Bartolucci, S
Rossi, M
Cannio, R
机构
[1] CNR, Ist Biochim Prot, I-80131 Naples, Italy
[2] Univ Naples Federico II, Dipartimento Chim Biol, Naples, Italy
关键词
GDP-mannose pyrophosphorylase; genome; mannose metabolism; cloning; overexpression;
D O I
10.1016/j.gene.2004.02.033
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
An open reading frame (ORF) encoding a putative GDP-mannose pyrophosphorylase (SsoGMPP) was identified on the genome sequence of Sulfolobus solfataricus P2, the predicted gene product showing high amino acid sequence homology to several archaeal, bacterial, and eukaryal GDP-mannose pyrophosphorylases such as guanidine diphosphomannose pyrophosphorylases (GMPPs) from Saccharomyces cerevisiae and Arabidopsis thaliana. The sequence was PCR amplified from genomic DNA of S. solfataricus P2 and heterologous gene expression obtained as a fusion to glutathione S-transferase in Escherichia coli, under conditions suitable to reduce the formation of inclusion bodies. Specific assays performed at 60degreesC revealed the presence of the archaeal synthesizing GDP-mannose enzyme activity in the cell extracts of the transformed E. coli. As a positive control. the same assays were performed at the mesophilic enzyme optimum temperature on the already characterized yeast recombinant GMPP. The recombinant protein was purified to homogeneity by glutathione sepharose affinity chromatography and its thermophilic nature could be verified. The enzyme was definitively identified by demonstrating its capability to catalyze also the reverse reaction of pyrophosphorolysis and, most interestingly, its high specificity for synthesizing GDP-mannose. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:149 / 157
页数:9
相关论文
共 50 条
  • [1] Purification and properties of mycobacterial GDP-mannose pyrophosphorylase
    Ning, B
    Elbein, AD
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1999, 362 (02) : 339 - 345
  • [2] Studies on the substrate specificity of a GDP-mannose pyrophosphorylase from Salmonella enterica
    Zou, Lu
    Zheng, Ruixiang Blake
    Lowary, Todd L.
    BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY, 2012, 8 : 1219 - 1226
  • [3] GDP-Mannose Pyrophosphorylase B (GMPPB)-Related Disorders
    Chompoopong, Pitcha
    Milone, Margherita
    GENES, 2023, 14 (02)
  • [4] Cloning, expression and characterization of the pig liver GDP-mannose pyrophosphorylase - Evidence that GDP-mannose and GDP-Glc pyrophosphorylases are different proteins
    Ning, BT
    Elbein, AD
    EUROPEAN JOURNAL OF BIOCHEMISTRY, 2000, 267 (23): : 6866 - 6874
  • [5] Structural insights into selective inhibition of leishmanial GDP-mannose pyrophosphorylase
    Li, Hang
    Ji, Tuo
    Sun, Qi
    Chen, Yao
    Xu, Weiya
    Huang, Chengdong
    CELL DISCOVERY, 2022, 8 (01)
  • [6] Ubiquitination contributes to the regulation of GDP-mannose pyrophosphorylase B activity
    Franzka, Patricia
    Mittag, Sonnhild
    Chakraborty, Abhijnan
    Huber, Otmar
    Huebner, Christian A.
    FRONTIERS IN MOLECULAR NEUROSCIENCE, 2024, 17
  • [7] Structural insights into selective inhibition of leishmanial GDP-mannose pyrophosphorylase
    Hang Li
    Tuo Ji
    Qi Sun
    Yao Chen
    Weiya Xu
    Chengdong Huang
    Cell Discovery, 8
  • [8] Functional characterization of GDP-mannose pyrophosphorylase from Leptospira interrogans serovar Copenhageni
    Diez, Matias D. Asencion
    Demonte, Ana
    Giacomelli, Jorge
    Garay, Sergio
    Rodrigues, Daniel
    Hofmann, Birgit
    Hecht, Hans-Juerguen
    Guerrero, Sergio A.
    Iglesias, Alberto A.
    ARCHIVES OF MICROBIOLOGY, 2010, 192 (02) : 103 - 114
  • [9] A cloning of cDNA for the GDP-mannose pyrophosphorylase in a coccolithophorid, Emiliania huxleyi
    Kayano, K
    Suzuki, I
    Shiraiwa, Y
    PLANT AND CELL PHYSIOLOGY, 2006, 47 : S31 - S31
  • [10] GDP-mannose pyrophosphorylase is essential in the bloodstream form of Trypanosoma brucei
    Denton, Helen
    Fyffe, Stewart
    Smith, Terry K.
    BIOCHEMICAL JOURNAL, 2010, 425 : 603 - 614