Mining with Microbes

Microbes are playing increasingly important roles in commercial mining operations, where they are being used in the “bioleaching” of copper, uranium, and gold ores. Direct leaching is when microbial metabolism changes the redox state of the metal being harvested, rendering it more soluble. Indirect leaching includes redox chemistry of other metal cations that are then coupled in chemical oxidation or reduction of the harvested metal ion and microbial attack upon and solubilization of the mineral matrix in which the metal is physically embedded. In addition, bacterial cells are used to detoxify the waste cyanide solution from gold-mining operations and as “absorbants” of the mineral cations. Bacterial cells may replace activated carbon or alternative biomass. With an increasing understanding of microbial physiology, biochemistry and molecular genetics, rational approaches to improving these microbial activities become possible

[1]  T. Kusano,et al.  Evidence for two sets of structural genes coding for ribulose bisphosphate carboxylase in Thiobacillus ferrooxidans , 1991, Journal of bacteriology.

[2]  C. Brierley Bioremediation of metal‐contaminated surface and groundwaters , 1990 .

[3]  W. V. Shaw,et al.  Inducible plasmid-determined resistance to arsenate, arsenite, and antimony (III) in escherichia coli and Staphylococcus aureus , 1981, Journal of bacteriology.

[4]  T. Kusano,et al.  Electrotransformation of Thiobacillus ferrooxidans with plasmids containing a mer determinant , 1992, Journal of bacteriology.

[5]  T. Kusano,et al.  Molecular cloning of the gene encoding Thiobacillus ferrooxidans Fe(II) oxidase. High homology of the gene product with HiPIP. , 1992, The Journal of biological chemistry.

[6]  A. P. Harrison The acidophilic thiobacilli and other acidophilic bacteria that share their habitat. , 1984, Annual review of microbiology.

[7]  G J Olsen,et al.  Evolutionary relationships among sulfur- and iron-oxidizing eubacteria , 1992, Journal of bacteriology.

[8]  T. Kusano,et al.  Nucleotide sequence of the Thiobacillus ferrooxidans chromosomal gene encoding mercuric reductase. , 1989, Gene.

[9]  Wang-ming Yan,et al.  Expression of Heterogenous Arsenic Resistance Genes in the Obligately Autotrophic Biomining Bacterium Thiobacillus ferrooxidans , 1994, Applied and environmental microbiology.

[10]  D. Rawlings,et al.  Construction of arsenic-resistant Thiobacillus ferrooxidans recombinant plasmids and the expression of autotrophic plasmid genes in a heterotrophic cell-free system , 1984 .

[11]  W. Yan,et al.  Plasmid and transposon transfer to Thiobacillus ferrooxidans , 1994, Journal of bacteriology.

[12]  D. Rawlings,et al.  Molecular genetics of Thiobacillus ferrooxidans. , 1994, Microbiological reviews.

[13]  Zhankun Wang,et al.  Transfer of IncP Plasmids to Extremely Acidophilic Thiobacillus thiooxidans , 1992, Applied and environmental microbiology.

[14]  A. Haines,et al.  Developments and innovations in bacterial oxidation of refractory ores , 1991 .

[15]  T. Kusano,et al.  The merR regulatory gene in Thiobacillus ferrooxidans is spaced apart from the mer structural genes , 1991, Molecular microbiology.

[16]  S. Silver,et al.  Resistance to arsenic compounds in microorganisms. , 1994, FEMS microbiology reviews.

[17]  T. Sugio,et al.  Role of a Ferric Ion-Reducing System in Sulfur Oxidation of Thiobacillus ferrooxidans , 1985, Applied and environmental microbiology.

[18]  A. E. Torma Biohydrometallurgy as an emerging technology , 1986 .

[19]  S. Silver,et al.  Gene regulation of plasmid- and chromosome-determined inorganic ion transport in bacteria. , 1992, Microbiological reviews.

[20]  S. Bröer,et al.  Orphan enzyme or patriarch of a new tribe: the arsenic resistance ATPase of bacterial plasmids , 1993, Molecular microbiology.