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Ten cyclopeptides were isolated from the 70 % ethanol extract of Lycii Cortex and identified by physical and chemical properties and various spectroscopic methods. They were named as lyciumin E (1), lyciumin G (2), lyciumin F (3), lyciumin B methyl ester (4), lyciumin A methyl ester (5), lyciumin C methyl ester (6), lyciumin A (7), lyciumin B (8), lyciumin C (9) and lyciumin D (10). Among them, compounds 1-3 were new cyclopeptides, compound 4 was a new natural product, and compounds 5 and 6 were first isolated from this plant. The anti-inflammatory activity and mechanism of compounds 7-9 were studied in vitro. The results showed that compounds 7-9 could play an anti-inflammatory role by inhibiting the expression of IL-6 and TNF-α mRNA in RAW264.7 inflammatory cells induced by LPS and reducing the secretion of NO, IL-6 and TNF-α in the cell supernatant.
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http://dx.doi.org/10.1016/j.fitote.2025.106765 | DOI Listing |
Fitoterapia
September 2025
School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, People's Republic of China; The Key Research Laboratory of "Exploring Effective Substance in Classic and Famous Prescriptions of Traditional Chinese Medicine", The State Administration of Traditional Chinese Me
Ten cyclopeptides were isolated from the 70 % ethanol extract of Lycii Cortex and identified by physical and chemical properties and various spectroscopic methods. They were named as lyciumin E (1), lyciumin G (2), lyciumin F (3), lyciumin B methyl ester (4), lyciumin A methyl ester (5), lyciumin C methyl ester (6), lyciumin A (7), lyciumin B (8), lyciumin C (9) and lyciumin D (10). Among them, compounds 1-3 were new cyclopeptides, compound 4 was a new natural product, and compounds 5 and 6 were first isolated from this plant.
View Article and Find Full Text PDFNat Chem Biol
April 2024
Department of Medicinal Chemistry, University of Michigan, Ann Arbor, MI, USA.
The biosynthetic dogma of ribosomally synthesized and posttranslationally modified peptides (RiPP) involves enzymatic intermolecular modification of core peptide motifs in precursor peptides. The plant-specific BURP-domain protein family, named after their four founding members, includes autocatalytic peptide cyclases involved in the biosynthesis of side-chain-macrocyclic plant RiPPs. Here we show that AhyBURP, a representative of the founding Unknown Seed Protein-type BURP-domain subfamily, catalyzes intramolecular macrocyclizations of its core peptide during the sequential biosynthesis of monocyclic lyciumin I via glycine-tryptophan crosslinking and bicyclic legumenin via glutamine-tyrosine crosslinking.
View Article and Find Full Text PDF3 Biotech
May 2022
Department of Plant Sciences, Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal, Udupi, Karnataka 576104 India.
Unlabelled: The present study illustrates the transformation ability of two wild-type bacterial strains of s (MTCC 532 and MTCC 2364) on the embryogenic callus and callus-derived plantlets of a threatened Indian orchid, . Co-culture of the bacterium with the explants gave marginal hairy root phenotype that failed to multiply in the culture medium. Some primary and secondary metabolites were subdued in infected explants.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
November 2018
Whitehead Institute for Biomedical Research, Cambridge, MA 02142;
The plant kingdom contains vastly untapped natural product chemistry, which has been traditionally explored through the activity-guided approach. Here, we describe a gene-guided approach to discover and engineer a class of plant ribosomal peptides, the branched cyclic lyciumins. Initially isolated from the Chinese wolfberry , lyciumins are protease-inhibiting peptides featuring an N-terminal pyroglutamate and a macrocyclic bond between a tryptophan-indole nitrogen and a glycine α-carbon.
View Article and Find Full Text PDFChin J Nat Med
January 2018
State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing 210009, China. Electronic address:
Two cyclopeptides, celogentin L (1) and its epimer lyciumin A (2) were firstly isolated from Celosia argentea L.. The planar structures of the two compounds were fully determined by spectroscopic data, including 1D-, 2D-NMR, and HR-ESI/MS.
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