Arsenic bioremediation potential of a new arsenite-oxidizing bacterium Stenotrophomonas sp. MM-7 isolated from soil
Abstract A new arsenite-oxidizing bacterium was isolated from a low arsenic-containing (8.8 mg $ kg^{−1} $) soil. Phylogenetic analysis based on 16S rRNA gene sequencing indicated that the strain was closely related to Stenotrophomonas panacihumi. Batch experiment results showed that the strain comp...
Ausführliche Beschreibung
Autor*in: |
Bahar, Md. Mezbaul [verfasserIn] |
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Format: |
Artikel |
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Sprache: |
Englisch |
Erschienen: |
2012 |
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Schlagwörter: |
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Anmerkung: |
© Springer Science+Business Media B.V. 2012 |
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Übergeordnetes Werk: |
Enthalten in: Biodegradation - Springer Netherlands, 1990, 23(2012), 6 vom: 04. Juli, Seite 803-812 |
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Übergeordnetes Werk: |
volume:23 ; year:2012 ; number:6 ; day:04 ; month:07 ; pages:803-812 |
Links: |
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DOI / URN: |
10.1007/s10532-012-9567-4 |
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OLC205040378X |
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10.1007/s10532-012-9567-4 doi (DE-627)OLC205040378X (DE-He213)s10532-012-9567-4-p DE-627 ger DE-627 rakwb eng 570 610 VZ 12 ssgn Bahar, Md. Mezbaul verfasserin aut Arsenic bioremediation potential of a new arsenite-oxidizing bacterium Stenotrophomonas sp. MM-7 isolated from soil 2012 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer Science+Business Media B.V. 2012 Abstract A new arsenite-oxidizing bacterium was isolated from a low arsenic-containing (8.8 mg $ kg^{−1} $) soil. Phylogenetic analysis based on 16S rRNA gene sequencing indicated that the strain was closely related to Stenotrophomonas panacihumi. Batch experiment results showed that the strain completely oxidized 500 μM of arsenite to arsenate within 12 h of incubation in a minimal salts medium. The optimum initial pH range for arsenite oxidation was 5–7. The strain was found to tolerate as high as 60 mM arsenite in culture media. The arsenite oxidase gene was amplified by PCR with degenerate primers. The deduced amino acid sequence showed the highest identity (69.1 %) with the molybdenum containing large subunit of arsenite oxidase derived from Bosea sp. Furthermore the amino acids involved in binding the substrate arsenite, were conserved with the arsenite oxidases of other arsenite oxidizing bacteria such as Alcaligenes feacalis and Herminnimonas arsenicoxydans. To our knowledge, this study constitutes the first report on arsenite oxidation using Stenotrophomonas sp. and the strain has great potential for application in arsenic remediation of contaminated water. Arsenic Arsenite oxidizing bacteria Arsenite oxidase gene ( ) Detoxification Megharaj, Mallavarapu aut Naidu, Ravi aut Enthalten in Biodegradation Springer Netherlands, 1990 23(2012), 6 vom: 04. Juli, Seite 803-812 (DE-627)130929395 (DE-600)1056014-2 (DE-576)026322242 0923-9820 nnns volume:23 year:2012 number:6 day:04 month:07 pages:803-812 https://doi.org/10.1007/s10532-012-9567-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-UMW SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 GBV_ILN_2016 GBV_ILN_4082 GBV_ILN_4219 AR 23 2012 6 04 07 803-812 |
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10.1007/s10532-012-9567-4 doi (DE-627)OLC205040378X (DE-He213)s10532-012-9567-4-p DE-627 ger DE-627 rakwb eng 570 610 VZ 12 ssgn Bahar, Md. Mezbaul verfasserin aut Arsenic bioremediation potential of a new arsenite-oxidizing bacterium Stenotrophomonas sp. MM-7 isolated from soil 2012 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer Science+Business Media B.V. 2012 Abstract A new arsenite-oxidizing bacterium was isolated from a low arsenic-containing (8.8 mg $ kg^{−1} $) soil. Phylogenetic analysis based on 16S rRNA gene sequencing indicated that the strain was closely related to Stenotrophomonas panacihumi. Batch experiment results showed that the strain completely oxidized 500 μM of arsenite to arsenate within 12 h of incubation in a minimal salts medium. The optimum initial pH range for arsenite oxidation was 5–7. The strain was found to tolerate as high as 60 mM arsenite in culture media. The arsenite oxidase gene was amplified by PCR with degenerate primers. The deduced amino acid sequence showed the highest identity (69.1 %) with the molybdenum containing large subunit of arsenite oxidase derived from Bosea sp. Furthermore the amino acids involved in binding the substrate arsenite, were conserved with the arsenite oxidases of other arsenite oxidizing bacteria such as Alcaligenes feacalis and Herminnimonas arsenicoxydans. To our knowledge, this study constitutes the first report on arsenite oxidation using Stenotrophomonas sp. and the strain has great potential for application in arsenic remediation of contaminated water. Arsenic Arsenite oxidizing bacteria Arsenite oxidase gene ( ) Detoxification Megharaj, Mallavarapu aut Naidu, Ravi aut Enthalten in Biodegradation Springer Netherlands, 1990 23(2012), 6 vom: 04. Juli, Seite 803-812 (DE-627)130929395 (DE-600)1056014-2 (DE-576)026322242 0923-9820 nnns volume:23 year:2012 number:6 day:04 month:07 pages:803-812 https://doi.org/10.1007/s10532-012-9567-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-UMW SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 GBV_ILN_2016 GBV_ILN_4082 GBV_ILN_4219 AR 23 2012 6 04 07 803-812 |
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10.1007/s10532-012-9567-4 doi (DE-627)OLC205040378X (DE-He213)s10532-012-9567-4-p DE-627 ger DE-627 rakwb eng 570 610 VZ 12 ssgn Bahar, Md. Mezbaul verfasserin aut Arsenic bioremediation potential of a new arsenite-oxidizing bacterium Stenotrophomonas sp. MM-7 isolated from soil 2012 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer Science+Business Media B.V. 2012 Abstract A new arsenite-oxidizing bacterium was isolated from a low arsenic-containing (8.8 mg $ kg^{−1} $) soil. Phylogenetic analysis based on 16S rRNA gene sequencing indicated that the strain was closely related to Stenotrophomonas panacihumi. Batch experiment results showed that the strain completely oxidized 500 μM of arsenite to arsenate within 12 h of incubation in a minimal salts medium. The optimum initial pH range for arsenite oxidation was 5–7. The strain was found to tolerate as high as 60 mM arsenite in culture media. The arsenite oxidase gene was amplified by PCR with degenerate primers. The deduced amino acid sequence showed the highest identity (69.1 %) with the molybdenum containing large subunit of arsenite oxidase derived from Bosea sp. Furthermore the amino acids involved in binding the substrate arsenite, were conserved with the arsenite oxidases of other arsenite oxidizing bacteria such as Alcaligenes feacalis and Herminnimonas arsenicoxydans. To our knowledge, this study constitutes the first report on arsenite oxidation using Stenotrophomonas sp. and the strain has great potential for application in arsenic remediation of contaminated water. Arsenic Arsenite oxidizing bacteria Arsenite oxidase gene ( ) Detoxification Megharaj, Mallavarapu aut Naidu, Ravi aut Enthalten in Biodegradation Springer Netherlands, 1990 23(2012), 6 vom: 04. Juli, Seite 803-812 (DE-627)130929395 (DE-600)1056014-2 (DE-576)026322242 0923-9820 nnns volume:23 year:2012 number:6 day:04 month:07 pages:803-812 https://doi.org/10.1007/s10532-012-9567-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-UMW SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 GBV_ILN_2016 GBV_ILN_4082 GBV_ILN_4219 AR 23 2012 6 04 07 803-812 |
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10.1007/s10532-012-9567-4 doi (DE-627)OLC205040378X (DE-He213)s10532-012-9567-4-p DE-627 ger DE-627 rakwb eng 570 610 VZ 12 ssgn Bahar, Md. Mezbaul verfasserin aut Arsenic bioremediation potential of a new arsenite-oxidizing bacterium Stenotrophomonas sp. MM-7 isolated from soil 2012 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer Science+Business Media B.V. 2012 Abstract A new arsenite-oxidizing bacterium was isolated from a low arsenic-containing (8.8 mg $ kg^{−1} $) soil. Phylogenetic analysis based on 16S rRNA gene sequencing indicated that the strain was closely related to Stenotrophomonas panacihumi. Batch experiment results showed that the strain completely oxidized 500 μM of arsenite to arsenate within 12 h of incubation in a minimal salts medium. The optimum initial pH range for arsenite oxidation was 5–7. The strain was found to tolerate as high as 60 mM arsenite in culture media. The arsenite oxidase gene was amplified by PCR with degenerate primers. The deduced amino acid sequence showed the highest identity (69.1 %) with the molybdenum containing large subunit of arsenite oxidase derived from Bosea sp. Furthermore the amino acids involved in binding the substrate arsenite, were conserved with the arsenite oxidases of other arsenite oxidizing bacteria such as Alcaligenes feacalis and Herminnimonas arsenicoxydans. To our knowledge, this study constitutes the first report on arsenite oxidation using Stenotrophomonas sp. and the strain has great potential for application in arsenic remediation of contaminated water. Arsenic Arsenite oxidizing bacteria Arsenite oxidase gene ( ) Detoxification Megharaj, Mallavarapu aut Naidu, Ravi aut Enthalten in Biodegradation Springer Netherlands, 1990 23(2012), 6 vom: 04. Juli, Seite 803-812 (DE-627)130929395 (DE-600)1056014-2 (DE-576)026322242 0923-9820 nnns volume:23 year:2012 number:6 day:04 month:07 pages:803-812 https://doi.org/10.1007/s10532-012-9567-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-UMW SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 GBV_ILN_2016 GBV_ILN_4082 GBV_ILN_4219 AR 23 2012 6 04 07 803-812 |
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arsenic bioremediation potential of a new arsenite-oxidizing bacterium stenotrophomonas sp. mm-7 isolated from soil |
title_auth |
Arsenic bioremediation potential of a new arsenite-oxidizing bacterium Stenotrophomonas sp. MM-7 isolated from soil |
abstract |
Abstract A new arsenite-oxidizing bacterium was isolated from a low arsenic-containing (8.8 mg $ kg^{−1} $) soil. Phylogenetic analysis based on 16S rRNA gene sequencing indicated that the strain was closely related to Stenotrophomonas panacihumi. Batch experiment results showed that the strain completely oxidized 500 μM of arsenite to arsenate within 12 h of incubation in a minimal salts medium. The optimum initial pH range for arsenite oxidation was 5–7. The strain was found to tolerate as high as 60 mM arsenite in culture media. The arsenite oxidase gene was amplified by PCR with degenerate primers. The deduced amino acid sequence showed the highest identity (69.1 %) with the molybdenum containing large subunit of arsenite oxidase derived from Bosea sp. Furthermore the amino acids involved in binding the substrate arsenite, were conserved with the arsenite oxidases of other arsenite oxidizing bacteria such as Alcaligenes feacalis and Herminnimonas arsenicoxydans. To our knowledge, this study constitutes the first report on arsenite oxidation using Stenotrophomonas sp. and the strain has great potential for application in arsenic remediation of contaminated water. © Springer Science+Business Media B.V. 2012 |
abstractGer |
Abstract A new arsenite-oxidizing bacterium was isolated from a low arsenic-containing (8.8 mg $ kg^{−1} $) soil. Phylogenetic analysis based on 16S rRNA gene sequencing indicated that the strain was closely related to Stenotrophomonas panacihumi. Batch experiment results showed that the strain completely oxidized 500 μM of arsenite to arsenate within 12 h of incubation in a minimal salts medium. The optimum initial pH range for arsenite oxidation was 5–7. The strain was found to tolerate as high as 60 mM arsenite in culture media. The arsenite oxidase gene was amplified by PCR with degenerate primers. The deduced amino acid sequence showed the highest identity (69.1 %) with the molybdenum containing large subunit of arsenite oxidase derived from Bosea sp. Furthermore the amino acids involved in binding the substrate arsenite, were conserved with the arsenite oxidases of other arsenite oxidizing bacteria such as Alcaligenes feacalis and Herminnimonas arsenicoxydans. To our knowledge, this study constitutes the first report on arsenite oxidation using Stenotrophomonas sp. and the strain has great potential for application in arsenic remediation of contaminated water. © Springer Science+Business Media B.V. 2012 |
abstract_unstemmed |
Abstract A new arsenite-oxidizing bacterium was isolated from a low arsenic-containing (8.8 mg $ kg^{−1} $) soil. Phylogenetic analysis based on 16S rRNA gene sequencing indicated that the strain was closely related to Stenotrophomonas panacihumi. Batch experiment results showed that the strain completely oxidized 500 μM of arsenite to arsenate within 12 h of incubation in a minimal salts medium. The optimum initial pH range for arsenite oxidation was 5–7. The strain was found to tolerate as high as 60 mM arsenite in culture media. The arsenite oxidase gene was amplified by PCR with degenerate primers. The deduced amino acid sequence showed the highest identity (69.1 %) with the molybdenum containing large subunit of arsenite oxidase derived from Bosea sp. Furthermore the amino acids involved in binding the substrate arsenite, were conserved with the arsenite oxidases of other arsenite oxidizing bacteria such as Alcaligenes feacalis and Herminnimonas arsenicoxydans. To our knowledge, this study constitutes the first report on arsenite oxidation using Stenotrophomonas sp. and the strain has great potential for application in arsenic remediation of contaminated water. © Springer Science+Business Media B.V. 2012 |
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container_issue |
6 |
title_short |
Arsenic bioremediation potential of a new arsenite-oxidizing bacterium Stenotrophomonas sp. MM-7 isolated from soil |
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https://doi.org/10.1007/s10532-012-9567-4 |
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Megharaj, Mallavarapu Naidu, Ravi |
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