The effects of incubation time, temperature, initial pH, and dye concentration on the indigo carmine decolorization activity of Pseudomonas aeruginosa ATCC 10145 and some factors on the decolorization potential of crude laccase enzyme obtained from Funalia trogii ATCC 200800 were comparatively investigated. This bacterium showed effective decolorization activity at all agitation and temperature values. Indigo carmine was greatly decolorized by P. aeruginosa at all pH values except pH 10. A decrease in decolorization activity occurred with increasing dye concentration, but this bacterium effectively decolorized the dye within 24 h. The decolorization process was through microbial metabolism, not biosorption. No decolorization or laccase activity could be obtained by the cell-free intracellular extract or culture filtrate of this bacterium. On the other hand, crude laccase effectively decolorized indigo carmine under highly acidic conditions, especially at pH 3.0 as 57% in 300 seconds. This activity decreased progressively due to the increase in pH values. In a short incubation period and at high temperature values, the crude laccase enzyme removed the color of the dye at 50 °C (56%), 60 °C (45%), and 70 °C (38%). These data are important for improving methods for decolorization of textile dyes used at high temperatures in various industrial applications.
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http://dx.doi.org/10.3906/biy-1807-48 | DOI Listing |
Urogynecology (Phila)
January 2025
From the Medical and Surgical Gynecology Department, Mayo Clinic College of Medicine, Mayo Clinic, Jacksonville, FL.
At the scrub sink, we discussed the best ways to evaluate for ureteric patency during cystoscopy. For decades, surgeons have been using intravenous indigo carmine for evaluating ureteric patency. Ten years ago, a shortage of indigo carmine halted production.
View Article and Find Full Text PDFLangmuir
December 2024
Department of Physical Chemistry, Faculty of Basic Science, Tarbiat Modares University, P.O. Box 14115-175, Tehran 21, I.R. of Iran.
The aim of this research is to explore the effectiveness of epoxy-resin@polypyrole composites as a corrosion inhibitor when applied as a coating on carbon steel 1018 in a 3.5 wt % sodium chloride electrolyte solution. The anticorrosion properties of these composite coatings can be optimized by manipulating their morphology.
View Article and Find Full Text PDFAnal Chem
December 2024
Department of Chemistry "Giacomo Ciamician", University of Bologna, Via Guaccimanni 42, 48121 Ravenna, Italy.
The present study describes an innovative approach for the study of time-dependent alteration processes. It combines an advanced hyperspectral imaging (HSI) system, to collect visible reflectance and fluorescence spectral data sets sequentially, with a tailored multiblock data processing method. This enables the modeling of chemical degradation maps and the early, spatially resolved detection of dye alteration in textiles.
View Article and Find Full Text PDFBiosci Biotechnol Biochem
December 2024
Graduate School of Advanced Technology and Science, Tokushima University, Tokushima, Japan.
Microbial indigo reduction is a key reaction in indigo dyeing; however, the mechanism of the interaction with indigo remains unclear. We hypothesized that lignin is a candidate substance that supports this interaction. The addition of lignin effectively enhanced the indigo reduction.
View Article and Find Full Text PDFIntern Med
November 2024
Division of Gastroenterology, Department of Internal Medicine, St. Marianna University School of Medicine, Japan.
Objective To evaluate the influence of sample collection time during esophagogastroduodenoscopy (EGD) on the accuracy of a newly approved point-of-care test (POCT)-based polymerase chain reaction kit for detecting Helicobacter pylori and clarithromycin susceptibility in gastric wash fluid. Methods Intragastric fluid was collected at three time points: Collection Time 1 (start of EGD), Collection Time 2 (during EGD), and Collection Time 3 (after indigo carmine spraying). POCT-based quantitative PCR (qPCR) targeting 23S rRNA domain V (2142/2143) was used to quantify H.
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