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Antimicrobial nano-assemblies of tryptocidine C, a tryptophan-rich cyclic decapeptide, from ethanolic solutions.
Kumar, Vikas; van Rensburg, Wilma; Snoep, Jacky L; Paradies, Henrich H; Borrageiro, Christopher; de Villiers, Carmen; Singh, Ramesh; Joshi, Khashti Ballabh; Rautenbach, Marina.
Affiliation
  • Kumar V; Department of Biochemistry, Stellenbosch University, Stellenbosch, 7600, South Africa.
  • van Rensburg W; Department of Biochemistry, Stellenbosch University, Stellenbosch, 7600, South Africa.
  • Snoep JL; Department of Biochemistry, Stellenbosch University, Stellenbosch, 7600, South Africa; Molecular Cell Biology, Vrije Universiteit Amsterdam, De Boelelaan 1105, 1081 HV, Amsterdam, the Netherlands.
  • Paradies HH; Jacobs-University, Department of Chemistry and Life Science, Bremen, 30110, Germany.
  • Borrageiro C; Department of Biochemistry, Stellenbosch University, Stellenbosch, 7600, South Africa.
  • de Villiers C; Department of Biochemistry, Stellenbosch University, Stellenbosch, 7600, South Africa.
  • Singh R; Department of Chemistry, Dr Harisingh Gour Vishwavidyalaya (A Central University), Sagar, MP, 470003, India.
  • Joshi KB; Department of Chemistry, Dr Harisingh Gour Vishwavidyalaya (A Central University), Sagar, MP, 470003, India.
  • Rautenbach M; Department of Biochemistry, Stellenbosch University, Stellenbosch, 7600, South Africa. Electronic address: mra@sun.ac.za.
Biochimie ; 204: 22-32, 2023 Jan.
Article in En | MEDLINE | ID: mdl-36057373
Tryptocidine C (TpcC), a Trp-rich cyclodecapeptide is a minor constituent in the antibiotic tyrothricin complex from Brevibacillus parabrevis. TpcC possesses a high tendency to oligomerise in aqueous solutions and dried TpcC forms distinct self-assembled nanoparticles. High-resolution scanning electron microscopy revealed the influence of different ethanol:water solvent systems on TpcC self-assembly, with the TpcC, dried from a high concentration in 15% ethanol, primarily assembling into small nanospheres with 24.3 nm diameter and 0.05 polydispersity. TpcC at 16 µM, near its CMC, formed a variety of structures such as small nanospheres, large dense nanospheroids and facetted 3-D-crystals, as well as sheets and coarse carpet-like structures which depended on ethanol concentration. Drying 16 µM TpcC from 75% ethanol resulted in highly facetted 3-D crystals, as well as small nanospheres, while those in 10% ethanol preparation had less defined facets. Drying from 20 to 50% ethanol led to polymorphic architectures with a few defined nanospheroids and various small nanoparticles, imbedded in carpet- and sheet-like structures. These polymorphic surface morphologies correlated with maintenance of fluorescence properties and the surface-derived antibacterial activity against Staphylococcus aureus over time, while there was a significant change in fluorescence and loss in activity in the 10% and 75% preparations where 3-D crystals were observed. This indicated that TpcC oligomerisation in solutions with 20-50% ethanol leads to metastable structures with a high propensity for release of antimicrobial moieties, while those leading to crystallisation limit active moieties release. TpcC nano-assemblies can find application in antimicrobial coatings, surface disinfectants, food packaging and wound healing materials.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tryptophan / Nanoparticles Language: En Journal: Biochimie Year: 2023 Type: Article Affiliation country: South Africa

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tryptophan / Nanoparticles Language: En Journal: Biochimie Year: 2023 Type: Article Affiliation country: South Africa