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1.
Molecules ; 29(5)2024 Feb 20.
Article in English | MEDLINE | ID: mdl-38474439

ABSTRACT

The leaves of Chrysanthemum indicum L. are known to have various bioactive compounds; however, industrial use is extremely limited. To overcome this situation by producing high-quality leaves with high bioactive content, this study examined the environmental factors affecting the phytochemical content and antioxidant activity using C. indicum leaves collected from 22 sites in Kochi Prefecture, Japan. Total phenolic and flavonoid content in the dry leaves ranged between 15.0 and 64.1 (mg gallic acid g-1) and 2.3 and 11.4 (mg quercetin g-1), while the antioxidant activity (EC50) of the 50% ethanol extracts ranged between 28.0 and 123.2 (µg mL-1) in 1,1-Diphenyl-2-picrylhydrazyl radical scavenging assay. Among the identified compounds, chlorogenic acid and 1,5-dicaffeoylquinic acid were the main constituents in C. indicum leaves. The antioxidant activity demonstrated a positive correlation with 1,5-dicaffeoylquinic acid (R2 = 0.62) and 3,5-dicaffeoylquinic acid (R2 = 0.77). The content of chlorogenic acid and dicaffeoylquinic acid isomers varied significantly according to the effects of exchangeable magnesium, cation exchange capacity, annual temperature, and precipitation, based on analysis of variance. The habitat suitability map using the geographical information system and the MaxEnt model predicted very high and high regions, comprising 3.2% and 10.1% of the total area, respectively. These findings could be used in future cultivation to produce high-quality leaves of C. indicum.


Subject(s)
Chrysanthemum , Cinnamates , Flavonoids , Flavonoids/chemistry , Antioxidants/chemistry , Polyphenols/analysis , Chlorogenic Acid/analysis , Chrysanthemum/chemistry , Plant Leaves/chemistry , Plant Extracts/chemistry
2.
Nat Prod Res ; 35(6): 1024-1028, 2021 Mar.
Article in English | MEDLINE | ID: mdl-31135222

ABSTRACT

Chemical isolation and bioactivity studies were conducted on the stamens of Mesua ferrea L., which are being used in a traditional skincare formulation in Myanmar. Rhusflavanone and mesuaferrone B were obtained as the main biflavonoids together with lupeol, five common flavonoids, and five phenolic compounds. After being identified by NMR and other spectroscopic analyses, these compounds were evaluated for their 1,1-diphenyl-2-picrylhydrazyl (DPPH)-radical scavenging, human leukocyte elastase inhibitory, and mushroom tyrosinase inhibitory activities. The two biflavonoids exhibited strong inhibitory activities against elastase and tyrosinase, but low DPPH-radical scavenging activities. The contents of rhusflavanone and mesuaferrone B in the stamens were 0.35 ± 0.04% and 0.55 ± 0.06%, respectively. Moreover, lupeol was considered to be a cosmetically important component of the stamens because of its high content and strong elastase inhibitory activity. Rhusflavanone was reported to be isolated from M. ferrea for the first time.


Subject(s)
Benzopyrans/isolation & purification , Benzopyrans/pharmacology , Biflavonoids/isolation & purification , Biflavonoids/pharmacology , Enzyme Inhibitors/pharmacology , Flowers/chemistry , Monophenol Monooxygenase/antagonists & inhibitors , Pancreatic Elastase/antagonists & inhibitors , Agaricales/enzymology , Benzopyrans/chemistry , Biflavonoids/chemistry , Enzyme Inhibitors/chemistry , Humans , Monophenol Monooxygenase/metabolism , Pancreatic Elastase/metabolism
3.
Molecules ; 25(23)2020 Nov 25.
Article in English | MEDLINE | ID: mdl-33255802

ABSTRACT

The growth and quality of licorice depend on various environmental factors, including the local climate and soil properties; therefore, its cultivation is often unsuccessful. The current study investigated the key factors that affect the contents of bioactive compounds of Glycyrrhiza glabra L. root and estimated suitable growth zones from collection sites in the Hatay region of Turkey. The contents of three bioactive compounds (glycyrrhizic acid, glabridin, and liquiritin), soil factors (pH, soil bearing capacity, and moisture content), and geographical information (slope, aspect, curvature, elevation, and hillshade) were measured. Meteorological data (temperature and precipitation) were also obtained. An analysis of variance (ANOVA) and multivariate analysis of variance (MANOVA) were performed on the data. The soil bearing capacity, moisture content, slope, aspect, curvature, and elevation of the study area showed statistically significant effects on the glycyrrhizic acid and liquiritin contents. A habitat suitability zone map was generated using a GIS-based frequency ratio (FR) model with spatial correlations to the soil, topographical, and meteorological data. The final map categorized the study area into four zones: very high (15.14%), high (31.50%), moderate (40.25%), and low suitability (13.11%). High suitability zones are recommended for further investigation and future cultivation of G. glabra.


Subject(s)
Ecosystem , Glycyrrhiza/chemistry , Phytochemicals/chemistry , Plant Extracts/chemistry , Chromatography, High Pressure Liquid , Geography , Molecular Structure , Phytochemicals/isolation & purification , Plant Extracts/isolation & purification , ROC Curve , Soil/chemistry , Turkey
4.
Nat Prod Res ; 30(8): 954-9, 2016.
Article in English | MEDLINE | ID: mdl-26375047

ABSTRACT

Three known iridoid glucosides (gentiournoside A, gentiournoside E and depressoside) were isolated from the flowers of Gentiana urnula Harry Sm. through activity-guided fractionations with a 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay. All three compounds exhibited excellent DPPH radical scavenging activities (IC50: 10-20 µmol L(-1)) comparable to that of ascorbic acid and Trolox. However, examination of the NMR data revealed that the reported chemical structure of depressoside, previously isolated from the leaves of G. depressa, needed correcting due to incorrect elucidation around C-7 of the iridane skeleton, and was corrected to 6-ß-(2,3-dihydroxyphenyl)-D-glucosyl 7-O-(2,3-dihydroxybenzoyl)-loganate. Depressoside exhibited a much higher scavenging activity against superoxide radicals (IC50: 45.5 µmol L(-1)) than the other two extracted compounds (IC50: more than 900 µmol L(-1)) due to the crucial presence of a pyrogallyl unit.


Subject(s)
Flowers/chemistry , Free Radical Scavengers/chemistry , Gentiana/chemistry , Iridoid Glucosides/chemistry , Molecular Structure , Plant Extracts/chemistry
5.
J Biosci Bioeng ; 113(1): 99-105, 2012 Jan.
Article in English | MEDLINE | ID: mdl-21940203

ABSTRACT

Modification of internal configuration of a bubble column, airlift and stirred tank reactor (10-200 L) was made for root cultures of Bupleurum falcatum L. Agitation with an impeller covered with partition mesh was ineffective for a 10-L modified reactor, because it caused intensive foaming and subsequent overflow of the culture medium even at a low rotation speed of 50 rpm and a low aeration rate of 0.1 vvm (volume per volume of medium). In contrast, efficient aeration through a ceramic sparger placed at the bottom of a 20-L bubble column reactor yielded approximately 25 g/L of dry roots and 500 mg/L of saikosaponin-a and saikosaponin-d over 42 days. On a 200-L scale, however, the roots became flocculated under the upper perforated plate initially positioned near the middle of the reactor, forming a firm disk of roots and a large empty space between the disk and the medium. Thus, the roots had poor contact with the medium, which severely suppressed their growth. To avoid this flocculation, a bottom perforated plate and draft tube were installed as a partitioning device separating the culturing area (outside the draft tube) from the aeration area (inside the draft tube). The draft tube was made of a stainless steel mesh rather than a solid material, and the tube greatly increased the root yield in the 20-L reactor. This configuration was successfully applied at the 200-L scale, yielding 500-600 mg/L of saikosaponin-a and saikosaponin-d over 56 days.


Subject(s)
Bioreactors , Bupleurum/metabolism , Oleanolic Acid/analogs & derivatives , Plant Roots/metabolism , Saponins/biosynthesis , Tissue Culture Techniques/methods , Bupleurum/growth & development , Culture Media/chemistry , Oleanolic Acid/biosynthesis , Plant Roots/growth & development , Tissue Culture Techniques/instrumentation
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