Microarray and bioinformatic analyses suggest models for carbon metabolism in the autotroph Acidithiobacillus ferrooxidans

被引:36
作者
Appia-Ayme, Corinne
Quatrini, Raquel
Denis, Yann
Denizot, Francois
Silver, Simon
Roberto, Francisco
Veloso, Felipe
Valdes, Jorge
Cardenas, Juan Pablo
Esparza, Mario
Orellana, Omar
Jedlicki, Eugenia
Bonnefoy, Violaine
Holmes, David S. [1 ]
机构
[1] Andres Bello Univ, Santiago, Chile
[2] Millennium Inst Fundamental & Appl Biol, Santiago, Chile
[3] CNRS, Chim Bacterienne Lab, IBSM, F-13277 Marseille, France
[4] Univ Illinois, Chicago, IL USA
[5] Idaho Natl Lab, Idaho Falls, ID USA
[6] Univ Santiago Chile, Santiago, Chile
[7] Univ Chile, Fac Med, ICBM, Santiago 7, Chile
基金
美国国家科学基金会;
关键词
Calvin cycle; glycogen; glycolate; carboxysome; genome of Acidithiobacillus ferrooxidans;
D O I
10.1016/j.hydromet.2006.03.029
中图分类号
TF [冶金工业];
学科分类号
0806 ;
摘要
Acidithiobacillus ferrooxidans is a chemolithoautotrophic bacterium that uses iron or sulfur as an energy and electron source. Bioinformatic analysis of the A. ferrooxidans draft genome sequence was used to identify putative genes and potential metabolic pathways involved in CO2 fixation, 2P-glycolate detoxification, carboxysome formation and glycogen utilization. Microarray transcript profiling was carried out to compare the relative expression of the predicted genes of these pathways when the microorganism was grown in the presence of iron versus sulfur. Several gene expression patterns were confirmed by real-time PCR. Genes for each of the above-predicted pathways were found to be organized into discrete clusters. Clusters exhibited differential gene expression depending on the presence of iron or sulfur in the medium. Concordance of gene expression within each cluster suggested that they are operons. Most notably, clusters of genes predicted to be involved in CO2 fixation, carboxysome formation, 2P-glycolate detoxification and glycogen biosynthesis were upregulated in sulfur medium, whereas genes involved in glycogen utilization were preferentially expressed in iron medium. These results can be explained in terms of models of gene regulation that suggest how A. ferrooxidans can adjust its central carbon management to respond to changes in its environment. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:273 / 280
页数:8
相关论文
共 28 条
[1]  
[Anonymous], 1989, ADV MICROB PHYSIOL
[2]   Evolution and diversity of CO2 concentrating mechanisms in cyanobacteria [J].
Badger, MR ;
Hanson, D ;
Price, GD .
FUNCTIONAL PLANT BIOLOGY, 2002, 29 (2-3) :161-173
[3]   RELATIONS BETWEEN D-RIBULOSE-1,5-BIS-PHOSPHATE CARBOXYLASE, CARBOXYSOMES AND CO2 FIXING CAPACITY IN THE OBLIGATE CHEMOLITHOTROPH THIOBACILLUS-NEAPOLITANUS GROWN UNDER DIFFERENT LIMITATIONS IN THE CHEMOSTAT [J].
BEUDEKER, RF ;
CANNON, GC ;
KUENEN, JG ;
SHIVELY, JM .
ARCHIVES OF MICROBIOLOGY, 1980, 124 (2-3) :185-189
[4]   CHARACTERIZATION OF A HOMOGENOUS PREPARATION OF CARBOXYSOMES FROM THIOBACILLUS-NEAPOLITANUS [J].
CANNON, GC ;
SHIVELY, JM .
ARCHIVES OF MICROBIOLOGY, 1983, 134 (01) :52-59
[5]   Organization of carboxysome genes in the thiobacilli [J].
Cannon, GC ;
Baker, SH ;
Soyer, F ;
Johnson, DR ;
Bradburne, CE ;
Mehlman, JL ;
Davies, PS ;
Jiang, QL ;
Heinhorst, S ;
Shively, JM .
CURRENT MICROBIOLOGY, 2003, 46 (02) :115-119
[6]   Microcompartments in prokaryotes: Carboxysomes and related polyhedra [J].
Cannon, GC ;
Bradburne, CE ;
Aldrich, HC ;
Baker, SH ;
Heinhorst, S ;
Shively, JM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (12) :5351-5361
[7]   ISOLATION AND CHARACTERIZATION OF A CARBOXYSOME SHELL GENE FROM THIOBACILLUS-NEAPOLITANUS [J].
ENGLISH, RS ;
LORBACH, SC ;
QIN, X ;
SHIVELY, JM .
MOLECULAR MICROBIOLOGY, 1994, 12 (04) :647-654
[8]   THE STRUCTURES AND RELATED FUNCTIONS OF PHOSPHORYLASE-A [J].
FLETTERICK, RJ ;
MADSEN, NB .
ANNUAL REVIEW OF BIOCHEMISTRY, 1980, 49 :31-61
[9]   EVIDENCE FOR CALVIN CYCLE AND HEXOSE MONOPHOSPHATE PATHWAY IN THIOBACILLUS FERROOXIDANS [J].
GALE, NL ;
BECK, JV .
JOURNAL OF BACTERIOLOGY, 1967, 94 (04) :1052-&
[10]   The molecular regulation of the reductive pentose phosphate pathway in Proteobacteria and Cyanobacteria [J].
Gibson, JL ;
Tabita, FR .
ARCHIVES OF MICROBIOLOGY, 1996, 166 (03) :141-150