Efficient degradation and detoxification of methylene blue dye by a newly isolated ligninolytic enzyme producing bacterium Bacillus albus MW407057

Colloids Surf B Biointerfaces. 2021 Oct:206:111947. doi: 10.1016/j.colsurfb.2021.111947. Epub 2021 Jun 26.

Abstract

In present work, a LiP enzyme producing bacterium was isolated form textile wastewater and sludge sample and identified as Bacillus albus by 16S rRNA gene sequencing analysis. This bacterium decolorized 99.27 % MB dye and removed 83.87 % COD within 6 h at 30 °C, pH 7, 100 rpm and 100 mg/l of dye concentration in presence of glucose and yeast extract as carbon and nitrogen source, respectively. The bacterium also produced LiP enzyme of molecular weight ∼48 kDa, characterized by SDS-PAGE analysis. Different metabolites like monomethylthionine, thionin, (E)-2-(3-Oxopropylidene)-2H-benzo[b][1,4] thiozine-3-carboxylic acid, N-(3,4-dihydroxyphenyl)-N-methylformamide, ethylamine, water and carbon dioxide produced during treatment process were characterized by FT-IR and LC-MS analysis. Further, the toxicity assessment results showed that the toxicity of bacteria treated dye solution was reduced significantly allowing 90 % seed germination indicating that the isolated bacterium B. albus has high potential to decolorize and detoxify MB dye for environmental safety.

Keywords: Degradation; LC–MS analysis; Lignin peroxidase; Methylene blue; Phytotoxicity.

MeSH terms

  • Bacillus
  • Bacteria
  • Biodegradation, Environmental
  • Coloring Agents*
  • Methylene Blue*
  • RNA, Ribosomal, 16S / genetics
  • Spectroscopy, Fourier Transform Infrared

Substances

  • Coloring Agents
  • RNA, Ribosomal, 16S
  • Methylene Blue

Supplementary concepts

  • Bacillus albus