5.9
CiteScore
5.9
Impact Factor
Volume 38 Issue 6
Jun.  2011
Turn off MathJax
Article Contents

Unraveling the Acidithiobacillus caldus complete genome and its central metabolisms for carbon assimilation

doi: 10.1016/j.jgg.2011.04.006
More Information
  • Corresponding author: E-mail address: jiangcy@im.ac.cn (Cheng-Ying Jiang); E-mail address: liusj@sun.im.ac.cn (Shuang-Jiang Liu)
  • Received Date: 2011-04-05
  • Accepted Date: 2011-04-20
  • Rev Recd Date: 2011-04-14
  • Available Online: 2011-05-14
  • Publish Date: 2011-06-20
  • Acidithiobacillus caldus is one of the dominant sulfur-oxidizing bacteria in bioleaching reactors. It plays the essential role in maintaining the high acidity and oxidation of reduced inorganic sulfur compounds during bioleaching process. In this report, the complete genome sequence of A. caldus SM-1 is presented. The genome is composed of one chromosome (2,932,225 bp) and four plasmids (pLAtc1, pLAtc2, pLAtc3, pLAtcm) and it is rich in repetitive sequences (accounting for 11% of the total genome), which are often associated with transposable genetic elements. In particular, twelve copies of ISAtfe and thirty-seven copies of ISAtc1 have been identified, suggesting that they are active transposons in the genome. A. caldus SM-1 encodes all enzymes for the central metabolism and the assimilation of carbon compounds, among which 29 proteins/enzymes were identifiable with proteomic tools. The SM-1 fixes CO2 via the classical Calvin–Bassham–Benson (CBB) cycle, and can operate complete Embden-Meyerhof pathway (EMP), pentose phosphate pathway (PPP), and gluconeogenesis. It has an incomplete tricarboxylic acid cycle (TCA). Four putative transporters involved in carbohydrate uptake were identified. Taken together, the results suggested that SM-1 was able to assimilate carbohydrates and this was subsequently confirmed experimentally because addition of 1% glucose or sucrose in basic salt medium significantly increased the growth of SM-1. It was concluded that the complete genome of SM-1 provided fundamental data for further investigation of its physiology and genetics, in addition to the carbon metabolism revealed in this study.
  • loading
  • [1]
    Azuma, Y., Hosoyama, A., Matsutani, M. et al. Nucleic Acid Res., 37 (2009),pp. 5768-5783
    [2]
    Bugaytsova, Z., Lindström, E.B. Eur. J. Biochem., 271 (2004),pp. 272-280
    [3]
    Chen, Z.W., Liu, Y.Y., Wu, J.F. et al. Novel bacterial sulfur oxygenase reductases from bioreactors treating gold-bearing concentrates Appl. Microbiol. Biotechnol., 74 (2007),pp. 688-698
    [4]
    Delcher, A.L., Bratke, K.A., Powers, E.C. et al. Identifying bacterial genes and endosymbiont DNA with Glimmer Bioinformatics, 23 (2007),pp. 673-679
    [5]
    Dopson, M., Lindström, E.B. Appl. Environ. Microbiol., 65 (1999),pp. 36-40
    [6]
    Dopson, M., Lindström, E.B., Hallberg, K.B. Extremophiles, 6 (2002),pp. 123-129
    [7]
    Edwards, K.J., Bond, P.L., Banfield, J.F. Environ. Microbiol., 2 (2000),pp. 324-332
    [8]
    Esparza, M., Cardenas, J.P., Bowien, B. et al. BMC Microbiol., 10 (2010),pp. 229-244
    [9]
    Fischer, F., Wolters, D., Rogner, M. et al. Toward the complete membrane proteome: high coverage of integral membrane proteins through transmembrane peptide detection Mol. Cell. Proteomics, 5 (2006),pp. 444-453
    [10]
    Golemis, E.A., Adams, P.D.
    [11]
    Haussmann, U., Qi, S.-W., Wolters, D. et al. Proteomics, 9 (2009),pp. 3635-3651
    [12]
    Kamimura, K., Okabayashi, A., Kikumoto, M. et al. Analysis of iron- and sulfur-oxidizing bacteria in a treatment plant of acid rock drainage from a Japanese pyrite mine by use of ribulose-1, 5-bisphosphate carboxylase/oxygenase large-subunit gene J. Biosci. Bioeng., 109 (2010),pp. 244-248
    [13]
    Kelly, D.P., Wood, A.P. Int. J. Syst. Evol. Microbiol., 50 (2002),pp. 511-516
    [14]
    Liu, Y.Y., Guo, X., Jiang, C.Y. Microbial diversity and characteristics of cultivable microorganisms in bioleaching reactors Acta Microbiol. Sin., 50 (2010),pp. 244-250
    [15]
    Mangold, S., Valdes, J., Holmés, D.S. et al. Front. Microbiol., 2 (2011),pp. 1-18
    [16]
    Marmur, J. A procedure for the isolation of deoxyribonucleic acid from microorganisms J. Mol. Biol., 3 (1961),pp. 208-218
    [17]
    Rzhepishevska, O.I., Valdés, J., Marcinkeviciene, L. et al. Appl. Environ. Microbiol., 73 (2007),pp. 7367-7372
    [18]
    Silverman, M.P., Lundgren, D.G. J. Bacteriol., 77 (1959),pp. 642-647
    [19]
    Spolaore, P., Joulian, C., Gouin, J. et al. Relationship between bioleaching performance, bacterial community structure and mineralogy in the bioleaching of a copper concentrate in stirred-tank reactors Appl. Microbiol. Biotechnol., 89 (2011),pp. 441-448
    [20]
    Tian, K.L., Lin, J.Q., Liu, X.M. et al. Biotechnol. Lett., 25 (2003),pp. 749-754
    [21]
    Valdes, J., Quatrini, R., Hallberg, K. et al. J. Bacteriol., 191 (2009),pp. 5877-5878
    [22]
    Watling, H.R. The bioleaching of sulphide minerals with emphasis on copper sulphides: a review Hydrometalllurgy, 84 (2006),pp. 81-108
    [23]
    Xia, L., Dai, S., Yin, C. et al. J. Ind. Microbiol. Biotechnol., 36 (2009),pp. 845-851
    [24]
    Zeng, W., Qiu, G., Zhou, H. et al. Community structure and dynamics of the free and attached microorganisms during moderately thermophilic bioleaching of chalcopyrite concentrate Bioresour. Technol., 101 (2010),pp. 7079-7086
    [25]
    Zhou, H.B., Zeng, W.M., Yang, Z.F. et al. Bioleaching of chalcopyrite concentrate by a moderately thermophilic culture in a stirred tank reactor Bioresour. Technol., 100 (2009),pp. 515-520
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Article Metrics

    Article views (51) PDF downloads (0) Cited by ()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return