Author response for "Immobilization of horseradish peroxidase onto Purolite® A109 and its anthraquinone dye biodegradation and detoxification potential"

Author(s):  
Nataša Ž. Šekuljica ◽  
Jelena R. Jovanović ◽  
Sonja M. Jakovetić Tanasković ◽  
Nevena D. Ognjanović ◽  
Ivana V. Gazikalović ◽  
...  
2020 ◽  
Vol 36 (4) ◽  
Author(s):  
Nataša Ž. Šekuljica ◽  
Jelena R. Jovanović ◽  
Sonja M. Jakovetić Tanasković ◽  
Nevena D. Ognjanović ◽  
Ivana V. Gazikalović ◽  
...  

2016 ◽  
Vol 70 (2) ◽  
pp. 217-224 ◽  
Author(s):  
Natasa Sekuljica ◽  
Nevena Prlainovic ◽  
Jelena Jovanovic ◽  
Andrea Stefanovic ◽  
Sanja Grbavcic ◽  
...  

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.


1991 ◽  
Vol 37 (12) ◽  
pp. 902-907 ◽  
Author(s):  
Maria B. Pasti ◽  
Don L. Crawford

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.


2020 ◽  
Author(s):  
Gesa F. Dinges ◽  
Alexander S. Chockley ◽  
Till Bockemühl ◽  
Kei Ito ◽  
Alexander Blanke ◽  
...  

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