Transcriptome profiling, cloning, and characterization of AnGlu04478, a Ginsenoside Hydrolyzing β-glucosidase from Aspergillus niger NG1306 DOI Creative Commons
Ming-Xing Jiang, Ling Zhu,

Shuhan Xie

и другие.

Research Square (Research Square), Год журнала: 2023, Номер unknown

Опубликована: Ноя. 21, 2023

Abstract Minor ginsenosides exhibit superior pharmacological activity compared to major ginsenosides, yet their presence in plants is limited. Therefore, it crucial efficiently obtain minor ginsenosides. Specific glycoside hydrolases offer the advantage of converting into specific counterparts under mild reaction conditions while minimizing structural damage. In this study, we utilized total extracted from Panax notoginseng leaves as substrates stimulate growth Aspergillus niger NG1306. Transcriptome analysis revealed that Anglu 04478 potentially participates biotransformation process Subsequently, was cloned and expressed Transetta (DE3). The An Glu04478 protein purified by Ni 2+ column its enzymatic properties were characterized. results show optimum pH 4.5 temperature 40°C, Cu had a certain inhibitory effect on Glu04478, other metal ions little it. tolerance ethanol, not significantly affected product (glucose) feedback inhibition. Using p NPG substrate, kinetic parameter K m 1.55 mmol/L, V max 0.014 mmol/min. test with substrate showed could selectively hydrolyze glucose ginsenoside Rb1, Rb2, Rb3 Rc at C3, putative metabolic pathway Rb1 → GypXVII, Rb2 C-O, C-Mx1 C-Mx, →C-Mc1.These findings indicate exhibits promiscuity β-glucosidase, thereby expanding options for biotransformation.

Язык: Английский

Bioconversion, Pharmacokinetics, and Therapeutic Mechanisms of Ginsenoside Compound K and Its Analogues for Treating Metabolic Diseases DOI Creative Commons
Md. Niaj Morshed, Reshmi Akter, Md Rezaul Karim

и другие.

Current Issues in Molecular Biology, Год журнала: 2024, Номер 46(3), С. 2320 - 2342

Опубликована: Март 11, 2024

Rare ginsenoside compound K (CK) is an intestinal microbial metabolite with a low natural abundance that primarily produced by physicochemical processing, side chain modification, or metabolic transformation in the gut. Moreover, CK exhibits potent biological activity compared to primary ginsenosides, which has raised concerns field of ginseng research and development, as well ginsenoside-related dietary supplements products. Ginsenosides Rb1, Rb2, Rc are generally used substrate generate via several bioconversion processes. Current shows wide range pharmacological actions, including boosting osteogenesis, lipid glucose metabolism, oxidation, insulin resistance, anti-inflammatory anti-apoptosis properties. Further on bioavailability toxicology can advance its medicinal application. The purpose this review lay groundwork for future clinical studies development therapy disorders. Furthermore, pharmacology investigated review. findings indicate modulates signaling pathways associated AMPK, SIRT1, PPARs, WNTs, NF-kB. It also demonstrates positive therapeutic effect non-alcoholic fatty liver disease (NAFLD), obesity, hyperlipidemia, diabetes, complications, osteoporosis. Additionally, analogues showed more bioavailability, less toxicity, efficacy against states. Enhancing regulating hazardous variables crucial use trials.

Язык: Английский

Процитировано

5

Targeted preparation of six rare ginsenosides using two β-glucosidases from Bifidobacterium adolescentis DOI
Yanbo Hu, Yiming Li,

Yuzhu Shen

и другие.

Food Bioscience, Год журнала: 2024, Номер 59, С. 104192 - 104192

Опубликована: Апрель 26, 2024

Язык: Английский

Процитировано

5

Synergistic effects of cellulase hydrolysis and multiplex-frequency ultrasonic-assisted treatment on powder promotion derived from Panax ginseng C.A Mayer leaves: a sustainable biotransformation strategy DOI

Yu-Wen Lin,

M.-H. Tsai, Dawei Huang

и другие.

Journal of Food Measurement & Characterization, Год журнала: 2025, Номер unknown

Опубликована: Май 16, 2025

Язык: Английский

Процитировано

0

Cell factories for methylerythritol phosphate pathway mediated terpenoid biosynthesis: An application of modern engineering towards sustainability DOI

G.Jean Kant,

Ashutosh Pandey, Ariba Hasan

и другие.

Process Biochemistry, Год журнала: 2024, Номер 139, С. 146 - 164

Опубликована: Фев. 5, 2024

Язык: Английский

Процитировано

3

Biosynthesis of Naringenin from p-Coumaric Acid in Engineering Oleaginous Filamentous Fungus Mucor circinelloides DOI
Xinyi Zan,

Yunting Xu,

G. Chen

и другие.

ACS Food Science & Technology, Год журнала: 2024, Номер 4(3), С. 747 - 756

Опубликована: Март 6, 2024

Oleaginous microorganisms have a large potential to be cell factory produce naringenin due their active fatty acid anabolism offering amounts of malonyl-CoA as the substrate for synthesis. However, only few studies reported production flavonoids in oleaginous microorganisms, e.g., Yarrowia lipolytica and Rhodosporidium toruloides. The fungus Mucor circinelloides produces β-carotene 15–36% dry weight lipids. This study is first time engineer an fungus, M. circinelloides, by heterologously expressing flavonoid biosynthetic genes 4CL, CHS, CHI recombinant product from p-coumaric acid. Limitation this present work that titer produced strains 2.2 mg/L degradation may exist circinelloides. Moreover, also provided three gene expression platform driven promoters transplant synthesis pathway interesting natural products into model Finally, multifunctional obtained effectively

Язык: Английский

Процитировано

3

A Versatile β-Glycosidase from Petroclostridium xylanilyticum Prefers the Conversion of Ginsenoside Rb3 over Rb1, Rb2, and Rc to Rd by Its Specific Cleavage Activity toward 1,6-Glycosidic Linkages DOI
Wenqi Xu,

Cuicui Duan,

Fumin Ma

и другие.

Journal of Agricultural and Food Chemistry, Год журнала: 2024, Номер 72(31), С. 17510 - 17523

Опубликована: Июль 25, 2024

To convert ginsenosides Rb1, Rb2, Rb3, and Rc into Rd by a single enzyme, putative β-glycosidase (Pxbgl) from the xylan-degrading bacterium Petroclostridium xylanilyticum was identified used. The kcat/Km value of Pxbgl for Rb3 18.18 ± 0.07 mM–1/s, which significantly higher than those other ginsenosides. converted almost all to with productivity 5884 μM/h, 346-fold that only β-xylosidase Thermoascus aurantiacus. Panax ginseng root notoginseng leaf 146 995 respectively. Mutants N293 K I447L site-directed mutagenesis based on bioinformatics analysis showed an increase in specific activity 29 7% toward This is first report can simultaneously remove four different glycosyls at C–20 position natural PPD-type produce as sole product P. extracts highest productivity.

Язык: Английский

Процитировано

3

Immobilization of snailase and β-glucosidase on L-aspartic acid-modified magnetic amorphous ZIF for efficiently and sustainably producing ginsenoside compound K DOI
S D Luo,

Duoduo Tian,

Ran Gao

и другие.

International Journal of Biological Macromolecules, Год журнала: 2024, Номер 291, С. 139230 - 139230

Опубликована: Дек. 26, 2024

Язык: Английский

Процитировано

2

Residue Effect-Guided Design: Engineering of S. Solfataricus β-Glycosidase to Enhance Its Thermostability and Bioproduction of Ginsenoside Compound K DOI
W C Shen, Paul A. Dalby,

Zheng Guo

и другие.

Journal of Agricultural and Food Chemistry, Год журнала: 2023, Номер 71(44), С. 16669 - 16680

Опубликована: Окт. 9, 2023

β-Glycosidase from Sulfolobus solfataricus (SS-BGL) is a highly effective biocatalyst for the synthesis of compound K (CK) glycosylated protopanaxadiol ginsenosides. In order to improve thermal stability SS-BGL, molecular dynamics simulations were used determine residue-level binding energetics ginsenoside Rd in SS-BGL-Rd docked complex and identify top ten critical contributors. Target sites mutations determined using dynamic cross-correlation mapping residues via Ohm server networks distal that interact with key residues. rationally based on site characteristics. Single mutants then recombination hits led two most promising variants SS-BGL-Q96E/N97D/N302D SS-BGL-Q96E/N97D/N128D/N302D 2.5-fold 3.3-fold increased half-lives at 95 °C, respectively. The enzyme activities relative those wild-type conversion 161 116%, respectively..

Язык: Английский

Процитировано

4

Bioconversion, Pharmacokinetics, and Therapeutic Mechanisms of Ginsenoside Compound K and Its Analogues for Treating Metabolic Diseases DOI Open Access
Md. Niaj Morshed, Reshmi Akter, Imran Mahmud

и другие.

Опубликована: Фев. 2, 2024

Rare ginsenoside compound K (CK), is an intestinal microbial metabolite with a low natural abundance that primarily produced by physicochemical processing, side chain modification, or metabolic transformation in the gut. Moreover, CK exhibits potent biological activity compared to primary ginsenosides, which has raised concerns field of ginseng research and development as well ginsenosides-related dietary supplements products. Ginsenosides Rb1, Rb2, Rc are generally used substrate generate via several bio-conversion processes. Current shows wide range pharmacological actions including boosting osteogenesis, lipid glucose metabolism, oxidation, insulin resistance, anti-inflammatory, anti-apoptosis properties. Further on bioavailability toxicology can advance its medicinal application. The purpose this review lay groundwork for future clinical studies therapy disorders. Furthermore, pharmacology investigated review. findings indicate modulates signal-ing pathways associated AMPK, SIRT1, PPARs, WNTs, NF-kB. It also demonstrates positive therapeutic effect nonalcoholic fatty liver disease, obesity, hyperlipidemia, diabetes, complications, osteoporosis. Additionally, analogues showed more bioavailability, less toxicity, efficacy against disease states. Enhancing regulating hazardous variables crucial use trials.

Язык: Английский

Процитировано

1

Immobilization of Bgps-Expressing Escherichia coli cells coated with ZIF-67 for the production of rare ginsenoside F1 DOI
Anni Zheng, Hao Liang

Biochemical Engineering Journal, Год журнала: 2024, Номер 210, С. 109432 - 109432

Опубликована: Июль 14, 2024

Язык: Английский

Процитировано

1