Reduction of Mo(VI) by the bacterium Serratia sp. strain DRY5

The need to isolate efficient heavy metal reducers for cost effective bioremediation strategy have resulted in the isolation of a potent molybdenum-reducing bacterium. The isolate was tentatively identified as Serratia sp. strain DRY5 based on the Biolog GN carbon utilization profiles and partial 16...

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Main Authors: Abdul Rahman, Mohd Fadhil, Abd. Shukor, Mohd. Yunus, Suhaili, Zarizal, Mustafa, Shuhaimi, Shamaan, Nor Aripin, Syed, Mohd Arif
Format: Article
Language:English
Published: Triveni Enterprises 2009
Online Access:http://psasir.upm.edu.my/id/eprint/16462/1/Reduction%20of%20Mo.pdf
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author Abdul Rahman, Mohd Fadhil
Abd. Shukor, Mohd. Yunus
Suhaili, Zarizal
Mustafa, Shuhaimi
Shamaan, Nor Aripin
Syed, Mohd Arif
author_facet Abdul Rahman, Mohd Fadhil
Abd. Shukor, Mohd. Yunus
Suhaili, Zarizal
Mustafa, Shuhaimi
Shamaan, Nor Aripin
Syed, Mohd Arif
author_sort Abdul Rahman, Mohd Fadhil
collection UPM
description The need to isolate efficient heavy metal reducers for cost effective bioremediation strategy have resulted in the isolation of a potent molybdenum-reducing bacterium. The isolate was tentatively identified as Serratia sp. strain DRY5 based on the Biolog GN carbon utilization profiles and partial 16S rDNA molecular phylogeny. Strain DRY5 produced 2.3 times the amount of Mo-blue than S. marcescens strain Dr.Y6, 23 times more than E. coli K12 and 7 times more than E. cloacae strain 48. Strain DRY5 required 37 degrees C and pH 7.0 for optimum molybdenum reduction. Carbon sources such as sucrose, maltose, glucose and glycerol, supported cellular growth and molybdate reduction after 24 hr of static incubation. The most optimum carbon source that supported reduction was sucrose at 1.0% (w/v). Ammonium sulphate, ammonium chloride, glutamic acid, cysteine, and valine supported growth and molybdate reduction with ammonium sulphate as the optimum nitrogen source at 0. 2% (w/v). Molybdate reduction was optimally supported by 30 mM molybdate. The optimum concentration of phosphate for molybdate reduction was 5 mM when molybdate concentration was fixed at 30 mM and molybdate reduction was totally inhibited at 100 mM phosphate. Mo-blue produced by this strain shows a unique characteristic absorption profile with a maximum peak at 865 nm and a shoulder at 700 nm, Dialysis tubing experiment showed that 95.42% of Mo-blue was found in the dialysis tubing suggesting that the molybdate reduction seen in this bacterium was catalyzed by enzyme(s). The characteristics of isolate DRY5 suggest that it would be useful in the bioremediation of molybdenum-containing waste.
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spelling upm.eprints-164622017-07-13T01:41:28Z http://psasir.upm.edu.my/id/eprint/16462/ Reduction of Mo(VI) by the bacterium Serratia sp. strain DRY5 Abdul Rahman, Mohd Fadhil Abd. Shukor, Mohd. Yunus Suhaili, Zarizal Mustafa, Shuhaimi Shamaan, Nor Aripin Syed, Mohd Arif The need to isolate efficient heavy metal reducers for cost effective bioremediation strategy have resulted in the isolation of a potent molybdenum-reducing bacterium. The isolate was tentatively identified as Serratia sp. strain DRY5 based on the Biolog GN carbon utilization profiles and partial 16S rDNA molecular phylogeny. Strain DRY5 produced 2.3 times the amount of Mo-blue than S. marcescens strain Dr.Y6, 23 times more than E. coli K12 and 7 times more than E. cloacae strain 48. Strain DRY5 required 37 degrees C and pH 7.0 for optimum molybdenum reduction. Carbon sources such as sucrose, maltose, glucose and glycerol, supported cellular growth and molybdate reduction after 24 hr of static incubation. The most optimum carbon source that supported reduction was sucrose at 1.0% (w/v). Ammonium sulphate, ammonium chloride, glutamic acid, cysteine, and valine supported growth and molybdate reduction with ammonium sulphate as the optimum nitrogen source at 0. 2% (w/v). Molybdate reduction was optimally supported by 30 mM molybdate. The optimum concentration of phosphate for molybdate reduction was 5 mM when molybdate concentration was fixed at 30 mM and molybdate reduction was totally inhibited at 100 mM phosphate. Mo-blue produced by this strain shows a unique characteristic absorption profile with a maximum peak at 865 nm and a shoulder at 700 nm, Dialysis tubing experiment showed that 95.42% of Mo-blue was found in the dialysis tubing suggesting that the molybdate reduction seen in this bacterium was catalyzed by enzyme(s). The characteristics of isolate DRY5 suggest that it would be useful in the bioremediation of molybdenum-containing waste. Triveni Enterprises 2009 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/16462/1/Reduction%20of%20Mo.pdf Abdul Rahman, Mohd Fadhil and Abd. Shukor, Mohd. Yunus and Suhaili, Zarizal and Mustafa, Shuhaimi and Shamaan, Nor Aripin and Syed, Mohd Arif (2009) Reduction of Mo(VI) by the bacterium Serratia sp. strain DRY5. Journal of Environmental Biology, 30 (1). pp. 65-72. ISSN 0254-8704; ESSN: 2394-0379 http://www.jeb.co.in/index.php?page=issue_toc&issue=200901_jan09_spl
spellingShingle Abdul Rahman, Mohd Fadhil
Abd. Shukor, Mohd. Yunus
Suhaili, Zarizal
Mustafa, Shuhaimi
Shamaan, Nor Aripin
Syed, Mohd Arif
Reduction of Mo(VI) by the bacterium Serratia sp. strain DRY5
title Reduction of Mo(VI) by the bacterium Serratia sp. strain DRY5
title_full Reduction of Mo(VI) by the bacterium Serratia sp. strain DRY5
title_fullStr Reduction of Mo(VI) by the bacterium Serratia sp. strain DRY5
title_full_unstemmed Reduction of Mo(VI) by the bacterium Serratia sp. strain DRY5
title_short Reduction of Mo(VI) by the bacterium Serratia sp. strain DRY5
title_sort reduction of mo vi by the bacterium serratia sp strain dry5
url http://psasir.upm.edu.my/id/eprint/16462/1/Reduction%20of%20Mo.pdf
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