Review for "Immobilization of horseradish peroxidase onto Purolite® <scp>A109</scp> and its anthraquinone dye biodegradation and detoxification potential"

The problem of environmental pollution day by day becomes more worrisome, primarily due to the large amounts of wastewater contaminated with various harmful organic compounds, discharged into the environment untreated or partially clean. Feasibility of use of horseradish peroxidase (Amoracia rusticana) in the synthetic dyes decolorization was approved by many researchers. Among a number of supports used for the immobilization, it was found that natural clay, kaolin has excellent features which are a precondition for obtaining biocatalysts with the excellent performances. For this reason, a horseradish peroxidase was immobilized onto kaolin using glutaraldehyde as a cross-linking agent. Obtained biocatalyst was applied in the decolorization of anthraquinone dye C. I. Acid Violet 109. Under determined optimal conditions (pH 4.0, hydrogen peroxide concentration 0.6 mM, dye concentration 30 mg L-1, temperature 24?C) around 76 % of dye decolorization was achieved. Reusability study showed that resulting biocatalyst was possible to apply four times in the desired reaction with relatively high decolorization percentage.

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Relationships between the abilities of streptomycetes to decolorize three anthron-type dyes and to degrade lignocellulose

Canadian Journal of Microbiology ◽

10.1139/m91-156 ◽

1991 ◽

Vol 37 (12) ◽

pp. 902-907 ◽

Cited By ~ 56

Author(s):

Maria B. Pasti ◽

Don L. Crawford

Keyword(s):

Solid State ◽

Horseradish Peroxidase ◽

Dye Decolorization ◽

Culture Broth ◽

Lignocellulose Degradation ◽

Poor Correlation ◽

Anthraquinone Dye ◽

Weight Losses ◽

Streptomyces Spp ◽

Complex Process

Fourteen Streptomyces strains known to degrade lignocellulose were screened for their ability to decolorize three anthron-type dyes: Remazol Brilliant Blue R (RBBR), blue poly(vinylamine) sulfonate – anthraquinone dye (Poly B-411), and red poly(vinylamine) sulfonate – anthrapyridone dye (Poly R-478). The relationships between efficiency of dye decolorization and capacity to attack lignocellulose were examined. Good correlation was found between lignocellulose weight losses observed during previous solid-state fermentation assays and the ability to decolorize RBBR and Poly B-411. A poor correlation was observed between Poly R-478 decolorizing activity and lignocellulose-degrading ability. The presence of corn stover lignocellulose in the culture broth enhanced decolorization of the dye by all but one of the strains. The enhancement was thought to involve the increased production of extracellular peroxidases by cultures growing on lignocellulose. The results on oxidation of the three dyes by a commercial horseradish peroxidase indicate that RBBR and Poly B-411 are suitable substrates for analyzing production of peroxidases by Streptomyces spp., while no decolorization of Poly R-478 was observed under the conditions used. However, Poly R-478 decolorizing activity of the Streptomyces may reflect the activity of other enzymes involved in the complex process of lignocellulose degradation. Key words: Streptomyces, lignocellulose, degradation, dye, decolorization.

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Effects of Vincristine on Endothelial Microtubules in the Spinal Cord

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100090270 ◽

1976 ◽

Vol 34 ◽

pp. 58-59

Author(s):

John L. Beggs ◽

John D. Waggener ◽

Wanda Miller

Keyword(s):

Spinal Cord ◽

Biological Activity ◽

Horseradish Peroxidase ◽

Transport Mechanism ◽

Vasogenic Edema ◽

Vesicular Transport ◽

Close Proximity

Microtubules (MT) are versatile organelles participating in a wide variety of biological activity. MT involvement in the movement and transport of cytoplasmic components has been well documented. In the course of our study on trauma-induced vasogenic edema in the spinal cord we have concluded that endothelial vesicles contribute to the edema process. Using horseradish peroxidase as a vascular tracer, labeled endothelial vesicles were present in all situations expected if a vesicular transport mechanism was in operation. Frequently,labeled vesicles coalesced to form channels that appeared to traverse the endothelium. The presence of MT in close proximity to labeled vesicles sugg ested that MT may play a role in vesicular activity.

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Comparative strengths and weaknesses of peroxidase and colloidal gold in pre- and post-embedding immunolabeling techniques

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100129279 ◽

1987 ◽

Vol 45 ◽

pp. 1002-1005

Author(s):

D. R. Abrahamson ◽

P. L. St.John ◽

E. W. Perry

Keyword(s):

Electron Microscopy ◽

Horseradish Peroxidase ◽

Light Microscopy ◽

Colloidal Gold ◽

Light Microscope ◽

Ultrastructural Localization ◽

The Other ◽

Quantitative Studies ◽

Dense Suspension ◽

Antigen Localization

Antibodies coupled to tracers for electron microscopy have been instrumental in the ultrastructural localization of antigens within cells and tissues. Among the most popular tracers are horseradish peroxidase (HRP), an enzyme that yields an osmiophilic reaction product, and colloidal gold, an electron dense suspension of particles. Some advantages of IgG-HRP conjugates are that they are readily synthesized, relatively small, and the immunolabeling obtained in a given experiment can be evaluated in the light microscope. In contrast, colloidal gold conjugates are available in different size ranges and multiple labeling as well as quantitative studies can therefore be undertaken through particle counting. On the other hand, gold conjugates are generally larger than those of HRP but usually can not be visualized with light microscopy. Concern has been raised, however, that HRP reaction product, which is exquisitely sensitive when generated properly, may in some cases distribute to sites distant from the original binding of the conjugate and therefore result in spurious antigen localization.

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