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1.
Molecules ; 24(10)2019 May 21.
Article in English | MEDLINE | ID: mdl-31117255

ABSTRACT

Lithospermic acid B (LSB), the major water-soluble ingredient of Salvia miltiorrhiza (Danshen), has been shown to be an active ingredient responsible for the therapeutic effects of this traditional Chinese herb used to treat cardiac disorders. This study aimed to develop an indirect competitive enzyme linked immunosorbent assay (ELISA) for the detection of LSB. Firstly, LSB was chemically conjugated to a modified oil-body protein, lysine-enriched caleosin, recombinantly expressed in Escherichia coli. Antibodies against LSB (Ab-LSB) were successfully generated by immunizing hens with artificial oil bodies constituted with the LSB-conjugated caleosin. Western blotting showed that Ab-LSB specifically recognized LSB, but not the carrier protein, lysine-enriched caleosin. To detect LSB via indirect competitive ELISA, LSB was conjugated with bovine serum albumin (LSB-BSA) and coated on a microplate. The binding between Ab-LSB and LSB-BSA on the microplate was competed dose-dependently in the presence of free LSB with a concentration ranging from 5 to 5 × 104 ng/mL. The IC50 value was approximately determined to be 120 ng/mL for LSB regardless of its complex with a metal ion of Na+, K+ or Mg2+.


Subject(s)
Antibodies/immunology , Benzofurans/isolation & purification , Depsides/isolation & purification , Enzyme-Linked Immunosorbent Assay , Salvia miltiorrhiza/chemistry , Antibodies/chemistry , Antibody Specificity/immunology , Benzofurans/chemistry , Benzofurans/immunology , Benzofurans/therapeutic use , Calcium-Binding Proteins/chemistry , Calcium-Binding Proteins/immunology , Depsides/chemistry , Depsides/immunology , Depsides/therapeutic use , Heart Diseases/drug therapy , Humans , Medicine, Chinese Traditional , Plant Proteins/chemistry , Plant Proteins/immunology
2.
J Food Drug Anal ; 26(2): 609-619, 2018 04.
Article in English | MEDLINE | ID: mdl-29567230

ABSTRACT

Phenolic compounds in a series of old oolong teas prepared by baking annually were monitored and compared. The results showed that the relative content of gallic acid over 5-galloylquinic acid was subsequently elevated during this preparatory process. To reveal the effect was mainly resulted from baking or aging, two sets of oolong teas were collected and examined; one set was generated from fresh oolong tea via continually daily baking and the other set was composed of aged oolong teas with no or light baking in the storage period. The relative content of gallic acid over 5-galloylquinic acid was observed to be subsequently elevated when oolong tea was continually baked at 90, 100, 110, and 120 °C for 8 h day after day. In contrast, the relative contents of gallic acid over 5-galloylquinic acid in aged oolong teas with no or light baking were found to be similar to or slightly higher than that in fresh oolong tea. The results suggest that the relative content of gallic acid over 5-galloylquinic acid seems to be a suitable index for the baking intensity of oolong tea in different preparations.


Subject(s)
Camellia sinensis/chemistry , Gallic Acid/analysis , Plant Leaves/chemistry , Quinic Acid/analysis , Cooking , Hot Temperature , Phenols/analysis
3.
J Food Drug Anal ; 25(4): 828-836, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28987359

ABSTRACT

Astringency, a sensory characteristic of food and beverages rich in polyphenols, mainly results from the formation of complexes between polyphenols and salivary proteins, causing a reduction of the lubricating properties of saliva. To develop an in vitro assay to estimate the astringency of oolong tea infusion, artificial oil bodies were constituted with sesame oil sheltered by a modified caleosin fused with histatin 3, one of the human salivary small peptides. Aggregation of artificial oil bodies was induced when they were mixed with oolong tea infusion or its major polyphenolic compound, (-)-epigallocatechin gallate (EGCG) of 100µM as observed in light microscopy. The aggregated artificial oil bodies gradually floated on top of the solution and formed a visible milky layer whose thickness was in proportion to the concentrations of tea infusion. This assay system was applied to test four different oolong tea infusions with sensory astringency corresponding to their EGCG contents. The result showed that relative astringency of the four tea infusions was correlated to the thickness of floated artificial oil bodies, and could be estimated according to the standard curve generated by simultaneously observing a serial dilution of the tea infusion with the highest astringency.


Subject(s)
Astringents/analysis , Calcium-Binding Proteins/analysis , Histatins/chemistry , Lipid Droplets/chemistry , Plant Proteins/analysis , Tea/chemistry , Calcium-Binding Proteins/genetics , Calcium-Binding Proteins/metabolism , Catechin/analogs & derivatives , Catechin/chemistry , Histatins/genetics , Histatins/metabolism , Humans , Plant Proteins/genetics , Plant Proteins/metabolism , Taste
4.
J Food Drug Anal ; 23(1): 71-81, 2015 Mar.
Article in English | MEDLINE | ID: mdl-28911448

ABSTRACT

The surface of a clay teapot tends to be coated with a waterproof film after constant use for tea preparation. The waterproof films of two kinds of teapots (zisha and zhuni) used for preparing oolong tea and old oolong tea were extracted and subjected to gas chromatography-mass spectrometry analysis. The results showed that comparable constituents were detected in these films; they were primarily fatty acids and linear hydrocarbons that were particularly rich in palmitic acid and stearic acid. To explore the source of these two abundant fatty acids, the fatty acid compositions of fresh tea leaves, granules, infusion, and vapor of infusion were analyzed by gas chromatography. Fresh tea leaves were rich in palmitic acid (C-16:0), unsaturated linolenic acid (C-18:3), linoleic acid (C-18:2), and oleic acid (C-18:1), which were presumably from the phospholipid membrane. During the process of manufacturing oolong tea, the three unsaturated fatty acids may be substantially degraded or oxidized to stearic acid (C-18:0), which was enriched with palmitic acid in the tea granules and in the infusion. The vapor of the tea infusion is primarily composed of palmitic acid and stearic acid. Thus, the coated films of teapots mostly originated from the lipophilic compounds of the tea infusions.

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