A mussel-inspired chitooligosaccharide based multidentate ligand for highly stabilized nanoparticles.

Inspired by the adhesion behaviors of mussels, we synthesized a chitooligosaccharide (COS) based multidentate ligand (ML) for preparing robust biocompatible magnetic iron oxide nanoparticles (IONPs). The COS was modified with mussel adhesive protein (MAP) mimetic multiple catechol groups and branched poly(ethylene glycol) moieties, which can not only strongly bind to IONPs through multiple catechol groups, but also afford IONPs with good colloidal stability and biocompatibility due to PEG integrated into the COS coating. The resultant ML-stabilized IONPs consist of single nanoparticles coated with ML shells and exhibited high dispersion stability in aqueous solution for a wide range of pH and concentrated salt solutions.

Distribution and abundance of Spirochaetes in full-scale anaerobic digesters.

To investigate the distribution and abundance of spirochaetal communities within anaerobic digesters, pyrosequencing of the 16S rRNA gene was conducted. Phylogenetic analysis identified a cluster which included the majority of core spirochaetal operational taxonomic units (OTUs) and environmental clones but no pure-culture strains. Distribution of the core OTUs demonstrated an importance of local factors in shaping the structure of Spirochaetes.

Monitoring bacterial community structure and variability in time scale in full-scale anaerobic digesters.

Using a high-throughput pyrosequencing technology, this study assessed bacterial community structure and time-scale variability in great detail in seven full-scale anaerobic digesters operated variously in terms of influent substrate, digestion temperature, and reactor configuration. Pyrosequencing generated a total of 83,774 sequence reads from 40 digester sludge samples collected monthly for six months. The highest number of sequence reads were detected within Proteobacteria (20.

Reductive decolorization of a textile reactive dyebath under methanogenic conditions.

The objective of the present study was to assess the biological decolorization of an industrial, spent reactive dyebath and its three dye components (Reactive Blue 19 [RB 19], Reactive Blue 21 [RB 21], and Reactive Red 198 [RR 198]) under methanogenic conditions. Using a mixed, methanogenic culture, batch assays were performed to evaluate the rate and extent of color removal as well as any potential toxic effects. Overall, a high rate and extent of color removal (>10 mg/[L.