Mycobacterium sp., Rhodococcus erythropolis, and Pseudomonas putida behavior in the presence of organic solvents

被引:49
作者
De Carvalho, CCCR
Da Cruz, AARL
Pons, MN
Pinheiro, HMRV
Cabral, JMS
Da Fonseca, MMR
Ferreira, BS
Fernandes, P
机构
[1] Inst Super Tecn, Ctr Engn Biol & Quim, P-1049001 Lisbon, Portugal
[2] Ecole Natl Super Ind Chim, Inst Natl Polytech Lorraine, CNRS, Lab Sci Genie Chim, F-54001 Nancy, France
[3] BioTrend Lda, P-2675807 Ramada, Portugal
[4] Univ Lusofona Humanidades & Tecnol, P-1749024 Lisbon, Portugal
关键词
organic solvent; fluorescence microscopy; image analysis; viability; morphology;
D O I
10.1002/jemt.20061
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
This work aimed at studying the behavior and tolerance of Mycobacterium sp. NRRL B-3805, Rhodococcus erythropolis DCL14 and Pseudomonas putida S 12 cells in the presence of various concentrations of water miscible (ethanol, butanol, and dimethylformamide, up to 50% v/v) and water immiscible solvents (dodecane, bis(2-ethylhexyl) phthalate and toluene, up to 5% v/v), When incubated in the presence of these solvents, the cells were found to have lower tolerance to butanol and toluene than to the remaining solvents. Nevertheless, the concentrations of solvents endured by the tested strains show that they are quite solvent-tolerant, confirming their potential as biocatalysts in nonconventional systems. Microscopic observation of samples showed that the hydrophobic Mycobacterium sp. and R. erythropolis cells were able to aggregate to protect the population under stress conditions. Comparison of the results obtained at the single cell level by fluorescence microscopy and colony development on agar plates indicated that the primary effects of most solvents tested were on the cell membrane and replicating capability of the cells. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:215 / 222
页数:8
相关论文
共 33 条
  • [1] Abe A, 1995, J MAR BIOTECHNOL, V2, P182
  • [2] Mycolic acids: Structure, biosynthesis and physiological functions
    Barry, CE
    Lee, RE
    Mdluli, K
    Sampson, AE
    Schroeder, BG
    Slayden, RA
    Yuan, Y
    [J]. PROGRESS IN LIPID RESEARCH, 1998, 37 (2-3) : 143 - 179
  • [3] Beney L, 2001, APPL MICROBIOL BIOT, V57, P34
  • [4] COWAN DA, 1992, PROGR BIOTECHNOL, V8, P623
  • [5] Whole-cell bioconversion of β-sitosterol in aqueous-organic two-phase systems
    Cruz, A
    Fernandes, P
    Cabral, JMS
    Pinheiro, HM
    [J]. JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC, 2001, 11 (4-6) : 579 - 585
  • [6] Two-phase partitioning bioreactors: a new technology platform for destroying xenobiotics
    Daugulis, AJ
    [J]. TRENDS IN BIOTECHNOLOGY, 2001, 19 (11) : 457 - 462
  • [7] Flow cytometry and cell sorting of heterogeneous microbial populations: The importance of single-cell analyses
    Davey, HM
    Kell, DB
    [J]. MICROBIOLOGICAL REVIEWS, 1996, 60 (04) : 641 - +
  • [8] Behaviour of Mycobacterium sp NRRL B-3805 whole cells in aqueous, organic-aqueous and organic media studied by fluorescence microscopy
    de Carvalho, CCCR
    Cruz, A
    Angelova, B
    Fernandes, P
    Pons, MN
    Pinheiro, HM
    Cabral, JMS
    da Fonseca, MMR
    [J]. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2004, 64 (05) : 695 - 701
  • [9] Principal components analysis as a tool to summarise biotransformation data: Influence on cells of solvent type and phase ratio
    de Carvalho, CCCR
    Pons, MN
    da Fonseca, MMR
    [J]. BIOCATALYSIS AND BIOTRANSFORMATION, 2003, 21 (06) : 305 - 314
  • [10] A simple method to observe organic solvent drops with a standard optical microscope
    De Carvalho, CCCR
    Da Fonseca, MMR
    [J]. MICROSCOPY RESEARCH AND TECHNIQUE, 2003, 60 (04) : 465 - 466