Isolation and characterization of indigenous copper-resistant actinomycete strains
Fifty actinomycetes were isolated from copper contaminated and non-contaminated area. Primary qualitative screening assays showed that 100% of the isolated microorganisms of the contaminated area were resistant up to 80 mg L −1 of CuSO 4. On the other hand, 100% of isolates from non-contaminated are...
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Published in | Chemie der Erde Vol. 65; pp. 145 - 156 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Elsevier GmbH
01.09.2005
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Subjects | |
Online Access | Get full text |
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Summary: | Fifty actinomycetes were isolated from copper contaminated and non-contaminated area. Primary qualitative screening assays showed that 100% of the isolated microorganisms of the contaminated area were resistant up to 80
mg
L
−1 of CuSO
4. On the other hand, 100% of isolates from non-contaminated area grew at 16
mg
L
−1, 87.4% at 40
mg
L
−1 and only 19.4% of them were capable of growing at 80
mg
L
−1 of CuSO
4. The semiquantitative assay showed that the isolated strains from the sediments of the contaminated site were resistant up to the highest concentration tested (1000
mg
L
−1) with the exception of AB2C strain; however, the strains isolated from non-contaminated sediments were sensitive to Cu
2+ concentrations higher than 200 and 400
mg
L
−1, respectively. Microbial growth of AB0 strain in presence of 39
mg
L
−1 copper showed an inhibition of 32% after 6 days of incubation as compared to the control, and copper residual concentration indicated a reduction in the supernatant of 71.2% after 6 days of incubation: pellet acid digestion proved that copper was accumulated by the cells. 16S rDNA restriction digestion of 1300
bp amplicons with
CfoI and
HpaII showed only one restriction pattern for all the strains and it matched with the control,
Streptomyces coelicolor. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0009-2819 1611-5864 |
DOI: | 10.1016/j.chemer.2005.06.004 |