Influence of the growth substrate on ester-linked phospho- and glycolipid fatty acids of PAH-degrading Mycobacterium sp LB501T

被引:32
作者
Wick, LY [1 ]
Pelz, O
Bernasconi, SM
Andersen, N
Harms, H
机构
[1] Swiss Fed Inst Technol, ENAC ISTE, Lab Soil Sci, EPFL, CH-1015 Lausanne, Switzerland
[2] Swiss Fed Inst Technol, Inst Terr Ecol, CH-8952 Schlieren, Switzerland
[3] Swiss Fed Inst Technol, Inst Geol, ETHZ, CH-8000 Zurich, Switzerland
关键词
D O I
10.1046/j.1462-2920.2003.00455.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The influences of poorly water-soluble anthracene on ester-linked phospholipid fatty acid (PLFA) and glycolipid fatty acid (GLFA) profiles of Mycobacterium sp. LB501T were studied. Bacteria were cultivated on either anthracene or glucose (one culture with successively amended small doses of this substrate and one with excess concentrations) to distinguish between influences of the chemical structure and the bioavailability of the growth substrate. Results revealed that GLFA and PLFA profiles of M . sp. LB501T depended on the availability and the structure of the carbon source. Fatty acid profiles obtained with anthracene differed from those obtained with excess glucose. They were interpreted as a specific adaptation to this poorly bioavailable polycyclic aromatic hydrocarbon (PAH). In contrast, profiles obtained with low glucose concentrations showed clear signs of starvation stress. Stable carbon isotopic ratios (delta(13) C) of GLFA and PLFA of M. sp. LB501T were analysed to characterize the (13) C-fractionation during the biosynthesis of individual fatty acids and to evaluate their value as markers for substrate usage. Although the delta(13) C values of PLFA and GLFA showed differential isotope fractionation during anthracene- and glucose-degradation, they were sufficiently distinct to be used as signatures of bacterial substrate usage.
引用
收藏
页码:672 / 680
页数:9
相关论文
共 40 条
[1]  
Abraham WR, 1998, APPL ENVIRON MICROB, V64, P4202
[2]  
[Anonymous], ISOT ENVIRON HEALT S, DOI DOI 10.1080/10256019808036364
[3]   EQUIVALENCE OF MICROBIAL BIOMASS MEASURES BASED ON MEMBRANE LIPID AND CELL-WALL COMPONENTS, ADENOSINE-TRIPHOSPHATE, AND DIRECT COUNTS IN SUBSURFACE AQUIFER SEDIMENTS [J].
BALKWILL, DL ;
LEACH, FR ;
WILSON, JT ;
MCNABB, JF ;
WHITE, DC .
MICROBIAL ECOLOGY, 1988, 16 (01) :73-84
[4]   Isolation of adherent polycyclic aromatic hydrocarbon (PAH)-degrading bacteria using PAH-sorbing carriers [J].
Bastiaens, L ;
Springael, D ;
Wattiau, P ;
Harms, H ;
deWachter, R ;
Verachtert, H ;
Diels, L .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (05) :1834-1843
[5]  
BAUGHMAN GL, 1981, CRC CRIT R MICROBIOL, P205
[6]  
Beney L, 2001, APPL MICROBIOL BIOT, V57, P34
[7]   CARBON ISOTOPIC FRACTIONATION IN HETEROTROPHIC MICROBIAL-METABOLISM [J].
BLAIR, N ;
LEU, A ;
MUNOZ, E ;
OLSEN, J ;
KWONG, E ;
DESMARAIS, D .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1985, 50 (04) :996-1001
[8]   The contribution of macrophyte-derived organic matter to microbial biomass in salt-marsh sediments: Stable carbon isotope analysis of microbial biomarkers [J].
Boschker, HTS ;
de Brouwer, JFC ;
Cappenberg, TE .
LIMNOLOGY AND OCEANOGRAPHY, 1999, 44 (02) :309-319
[9]   Stable isotopes and biomarkers in microbial ecology [J].
Boschker, HTS ;
Middelburg, JJ .
FEMS MICROBIOLOGY ECOLOGY, 2002, 40 (02) :85-95
[10]   Significance of carbon isotope discrimination between bulk carbon and extracted phospholipid fatty acids in selected terrestrial and marine environments [J].
Cifuentes, LA ;
Salata, GG .
ORGANIC GEOCHEMISTRY, 2001, 32 (04) :613-621