Objective: To study the β-glucosidase gene (bgy1) from Lactobacillus brevis that was cloned and expressed in Escherichia coli BL21 (DE3) and then using it for the biotransformation of gypenoside XVII.
Results: The bgy1 gene consists of 2283 bp encoding 761 amino acids, with homology to the glycosyl hydrolase family-3 protein domain. The enzyme (Bgy1) hydrolyzed the glucose moieties at the C-3 position and the outer glucose moieties at the C-20 position of gypenoside XVII. Using 0.1 mg enzyme ml(-1) in 20 mM sodium phosphate buffer at 30 °C and pH 6.0, 1 mg gypenoside XVII ml(-1) was transformed into 0.58 mg compound K ml(-1) within 6 h, with a corresponding molar conversion yield of 89 %.
Conclusion: The recombinant Bgy1 is considered potentially useful for the practical preparation of compound K.
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http://dx.doi.org/10.1007/s10529-016-2094-3 | DOI Listing |
J Pharm Biomed Anal
January 2025
School of Pharmacy, Fujian Medical University, Fuzhou, Fujian 350122, China. Electronic address:
Pien-Tze-Huang (PTH) is a famous traditional Chinese patent medicine with excellent liver-protection effects. However, the mechanism of hepatoprotective action has not yet been entirely elucidated. This study aimed to elucidate the protective mechanism of PTH against alcoholic liver injury in rats from key targets.
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October 2024
Institute of Special Animal and Plant, Chinese Academy of Agricultural Sciences, Changchun, China.
Arch Microbiol
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Hanbangbio Inc, Yongin-si, Gyeonggi-do, 17104, Republic of Korea.
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Department of Neurology, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China.
Background: Alzheimer's disease (AD) pathogenesis is complex. The pathophysiology is not fully understood, and safe and effective treatments are needed. Glycogen synthase kinase 3β (GSK-3β) mediates AD progression through several signaling pathways.
View Article and Find Full Text PDFBiomolecules
May 2024
School of Medicine, Fu Jen Catholic University, New Taipei 24205, Taiwan.
Excitotoxicity is a common pathological process in neurological diseases caused by excess glutamate. The purpose of this study was to evaluate the effect of gypenoside XVII (GP-17), a gypenoside monomer, on the glutamatergic system. In vitro, in rat cortical nerve terminals (synaptosomes), GP-17 dose-dependently decreased glutamate release with an IC value of 16 μM.
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