Valorization of leftover green tea residues through conversion to bioactive peptides using probiotics-aided anaerobic digestion.
Ji-Young LeeHyein HongJae-Eun LeeYi-Jee HongHye Won HwangHyeon-Su JinHyunkyou ShimYong-Deok HongWon-Seok ParkJin-Oh ChungDong-Woo LeePublished in: Microbial biotechnology (2022)
Bioactive peptides (BPs) are protein fragments that benefit human health. To assess whether leftover green tea residues (GTRs) can serve as a resource for new BPs, we performed in silico proteolysis of GTRs using the BIOPEP database, revealing a wide range of BPs embedded in GTRs. Comparative genomics and the percentage of conserved protein analyses enabled us to select a few probiotic strains for GTR hydrolysis. The selected probiotics digested GTRs anaerobically to yield GTR-derived peptide fractions. To examine whether green tea (GT) peptide fractions could be potential mediators of host-microbe interactions, we comprehensively screened agonistic and antagonistic activities of 168 human G protein-coupled receptors (GPCRs). NanoLC-MS/MS analysis and thin-layer chromatography allowed the identification of peptide sequences and the composition of glycan moieties in the GTRs. Remarkably, GT peptide fractions produced by Lactiplantibacillus plantarum APsulloc 331261, a strain isolated from GT, showed a potent-binding activity for P2RY6, a GPCR involved in intestinal homeostasis. Therefore, this study suggests the potential use of probiotics-aided GTR hydrolysates as postbiotic BPs, providing a biological process for recycling GTRs from agro-waste into renewable resources as health-promoting BPs.
Keyphrases
- human health
- anaerobic digestion
- risk assessment
- sewage sludge
- ms ms
- amino acid
- climate change
- endothelial cells
- heavy metals
- healthcare
- public health
- binding protein
- municipal solid waste
- mass spectrometry
- protein protein
- mental health
- molecular docking
- single cell
- high performance liquid chromatography
- liquid chromatography tandem mass spectrometry
- high speed
- simultaneous determination
- high resolution
- induced pluripotent stem cells
- dna binding