Characterization of a Novel Salt Tolerant Bacterium Gracilibacillus sp. GTY and Its Performance of Dye Decolorization

Characterization of a Novel Salt Tolerant Bacterium Gracilibacillus sp. GTY and Its Performance of Dye Decolorization

论文摘要

The main aim of this research work was to decolorize various azo dyes and reactive dyes from lab-scale dye solutions and real textile wastewater samples under high salt concentration conditions. Decolorization experiments were run using a recently isolated halophilic bacterium Gracilibacillus sp. GTY. As a new bacterial strain, some other investigations, such as isolation, characterization and study of a large extrachromosomal DNA were also taken place. So the dissertation is presented in different steps bellow.Firstly, a highly salt tolerant strain obtained from Dalian coastline, was identified as Gracilibacillus sp. GTY on the basis of morphological and physio-biochemical characteristics and 16S rDNA sequence analysis. According to DNA sequence, the maximum 93%-95% homology was found for the strain GTY. The strain was deposited as a patent strain in China General Microorganism Culture Center with the accession number CGMCC 1527. The 16S rDNA sequence of GTY was also submitted to GenBank with the number DQ 286727. The strain was gram-negative, rod-shaped and strictly aerobic. Optimum growth conditions were observed: temperature±30℃, pH 7.2, 10%-15% (w/v) of NaCl, and proline as the best compatible solute as well as a good carbon source. The rapid and smooth growth rates were observed in 10%-15% (w/v) of NaCl supplemented Luria-Bertani (LB) and Mineral-Salt (MS) media, but the strain could survive narrowly in the media containing up to 25% (w/v) of NaCl. So it was considered as a highly salt tolerant strain. Secondly, a large molecule of extrachromosomal DNA was isolated from the strain by a modified method. Then this plasmid DNA was eliminated by acridine orange to know its role in host genome. After successful elimination, it was assumed that the plasmid contains some key genes, which may be responsible for the bacterial salt tolerance.Thirdly, an attempt was made to optimize conditions for the bacterial decolorization of various dyes in lab-scale dye solutions under high salinity conditions. Decolorization experiments were conducted by growing and resting cells as well as azo reductase. Experiments were performed under different concentrations of NaCl. Detailed analytical investigations were performed using only one of the azo dyes, Acid Red B. For growing cells, strain grown in media containing10%-15% (w/v) of NaCl showed the best performance of azo dye Acid Red B decolorization. Dye was almost completely decolorized (nearly 100%) after 96 h of treatment. Strain grown in the media containing 2%-5% (w/v) of NaCl showed very poor decolorization ability where bacterial growth rates were very poor also. On the other hand, strain grown in the media with the highest percentage (25%, w/v) of NaCl showed moderate decolorization ability. Strain grown in lower percentages of NaCl could not show good performance of decolorization because of low growth rates. Decolorization was not satisfactory also in the media containing 25% (w/v) of NaCl, because the inhibition to microorganisms by high salt concentration, which may cause plasmolysis and /or loss of activity of cells. Resting cells also showed the best performance of decolorization in 10%-15% (w/v) of NaCl. Extracted azo reductase was non-purified and non-characterized. The decolorization of dye was conducted in 3 ml of reaction mixture at 30°C in 700 sec. Reaction rate obtained from time course spectra measurement analysis was comparatively slow. The percentage of dye removal was about 10% in the reaction mixture.Finally, several experiments were set up to degrade a textile azo dye Acid Red B and remove COD from a real textile wastewater body. The textile wastewater sample was naturally salty (10% of Na2SO4), and COD value was relatively high. The textile wastewater sample was used by adding certain nutrients and NaCl for the proper growth of this salt tolerant strain. The study was conducted on the basis of various environmental factors and substrates. Dye degradation and COD removal rates were comparatively slow in first two days. Decolorization efficiency might be attributed to the microbial shock due to the change of environment and the possible toxic or inhibitory effects of certain compounds of the textile wastewater on the microbe. Nevertheless, after an acclimatization period of 6-10 days, the anaerobic microbes retained their activity leading to wastewater’s decolorization efficiency of nearly 96% in optimum growth condition. Then COD removal rate was also satisfied. After decolorization, COD removal was observed 4436.87 (mg/l) where the initial COD value was more than 7000 (mg/l).

论文目录

  • Abstract
  • Acknowledgements
  • List of Tables
  • List of Figures
  • 1.Introduction
  • 2.Historical Background
  • 2.1.Salt Tolerant Bacteria
  • 2.1.1.Compatible solutes
  • 2.1.1.1.Proline
  • 2.1.2.Large extrachromosomal DNA
  • 2.2.Azo Dyes
  • 2.3.Reactive Azo Dyes
  • 2.4.Toxicity of Azo Dyes and Aromatic Amines
  • 2.5.Biotransformation of Azo Dyes
  • 2.5.1.Biotransformation of azo dyes under aerobic conditions
  • 2.5.2.Biotransformation of azo dyes under anaerobic conditions
  • 2.5.3.Biotransformation of reactive azo dyes
  • 2.5.4.Treatment of azo dye containing wastewaters
  • 3.Phases of Study
  • 3.1.Phase Ⅰ
  • 3.2.Phase Ⅱ
  • 3.3.Phase Ⅲ
  • 3.4.Phase Ⅳ
  • 3.5.Phase Ⅴ
  • 4.Isolation,Identification and Characterization of the Bacterial Strain Gracilibacillus sp.GTY
  • 4.1.Introduction
  • 4.2.Materials and Methods
  • 4.2.1.Media and culture conditions
  • 4.2.2.Extraction of genomic DNA,16S rDNA PCR,sequencing and phylogenic analysis
  • 4.3.Results and Discussion
  • 4.3.1.Isolation,identification and characterization
  • 4.3.1.1.Growth characteristics of GTY
  • 4.3.1.1.1.Effect of NaCl concentrations on growth
  • 4.3.1.1.2.Effect of pH variations on growth
  • 4.3.1.1.3.Screening of compatible solutes
  • 4.4.Conclusions
  • 5.Study of Large Extrachromosomal DNA
  • 5.1.Introduction
  • 5.2.Materials and Methods
  • 5.2.1.Media and culture condition
  • 5.2.2.Isolation technique of the extrachromosomal DNA
  • 5.2.3.Elimination technique of the extrachromosomal DNA
  • 5.2.4.Estimation
  • 5.3.Results and Discussion
  • 5.3.1.Isolation of the extrachromosomal DNA
  • 5.3.2.Elimination of the extrachromosomal DNA
  • 5.3.3.Effect of this extrachromosomal DNA on the host bacterial salt tolerance,dye decolorization and antibiotic sensitivity
  • 5.4.Conclusions
  • 6.Selection and Characterization of the Dyes
  • 6.1.Introduction
  • 6.2.Characterization of used dyes
  • 6.3.Selection of Acid Red B for more detailed investigations
  • 6.3.1.Effect of salt on UV-visible spectrum of Acid Red B
  • 7.Decolorization of Various Dyes(lab-scale dye solutions)by the Strain GTY
  • 7.1.Introduction
  • 7.2.Materials and Methods
  • 7.2.1.Media and culture conditions
  • 7.2.2.Decolorization by growing cells
  • 7.2.2.1.Decolorization in anaerobic liquid media
  • 7.2.2.2.Decolorization on agar plate
  • 7.2.3.Decolorization by resting cells
  • 7.2.4.Decolorization by extracted azo reductase
  • 7.2.5.Assay
  • 7.3.Results and Discussion
  • 7.3.1.Decolorization of the used dyes by growing cells
  • 7.3.2.Decolorization of selected azo dye Acid Red B by growing cells
  • 7.3.2.1.Decolorization of Acid Red B on LB agar plate versus in LB liquid media
  • 7.3.2.2.Decolorization under different NaCl concentrations
  • 7.3.2.3.Effect of carbon source on decolorization
  • 7.3.2.4.Effect of pH on decolorization
  • 7.3.2.5.Effect of light on decolorization
  • 7.3.3.Decolorization of selected azo dye Acid Red B by resting cells.
  • 7.3.4.Decolorization of selected azo dye Acid Red B by extracted azo reductase
  • 7.4.Conclusions
  • 8.Treatment of Real Textile Wastewater by the Strain GTY
  • 8.1.Introduction
  • 8.2.Materials and Methods
  • 8.2.1.Textile wastewater
  • 8.2.2.Operation technique
  • 8.2.3.Analytical methods
  • 8.3.Results and Discussion
  • 8.3.1.Decolorization of textile wastewater samples
  • 8.3.2.Decolorization and COD removal in presence and absences of carbon sources
  • 8.3.3.Effect of pH on decolorization and COD removal
  • 8.3.4.Effect of temperature on decolorization and COD removal
  • 8.4.Conclusions
  • 9.Conclusions and Recommendations for Further Studies
  • References
  • Scientific Articles
  • Appendix Ⅰ:Abbreviations
  • Appendix Ⅱ:16S rDNA Sequence Survey of the Strain GTY
  • Appendix Ⅲ:GenBank of 16S rDNA Sequence of the Strain GTY
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