ABSTRACT
Previous studies have revealed that gypenosides produced from Gynostemma pentaphyllum (Thunb.) Makino are mainly dammarane-type triterpenoid saponins with diverse structures and important biological activities, but the mechanism of diversity for gypenoside biosynthesis is still unclear. In this study, a combination of isobaric tags for relative and absolute quantification (iTRAQ) proteome analysis and RNA sequencing transcriptome analysis was performed to identify the proteins and genes related to gypenoside biosynthesis. A total of 3925 proteins were identified by proteomic sequencing, of which 2537 were quantified. Seventeen cytochrome P450 (CYP) and 11 uridine 5'-diphospho-glucuronosyltransferase (UDP-glucuronosyltransferase, UGT) candidate genes involved in the side chain synthesis and modification of gypenosides were found. Seven putative CYPs (CYP71B19, CYP77A3, CYP86A7, CYP86A8, CYP89A2, CYP90A1, CYP94A1) and five putative UGTs (UGT73B4, UGT76B1, UGT74F2, UGT91C1 and UGT91A1) were selected as candidate structural modifiers of triterpenoid saponins, which were cloned for gene expression analysis. Comprehensive analysis of RNA sequencing and proteome sequencing showed that some CYPs and UGTs were found at both the transcription and translation levels. In this study, an expression analysis of 7 CYPs and 5 UGTs that contributed to gypenoside biosynthesis and distribution in G. pentaphyllum was performed, providing consistent results that will inspire more future research on vital genes/proteins involved in gypenoside biosynthesis.
Subject(s)
Cytochrome P-450 Enzyme System/genetics , Glucuronosyltransferase/genetics , Gynostemma/growth & development , Chromatography, Liquid , Cloning, Molecular , Cytochrome P-450 Enzyme System/metabolism , Gene Expression Profiling , Gene Expression Regulation, Neoplastic , Glucuronosyltransferase/metabolism , Gynostemma/genetics , Gynostemma/metabolism , Plant Extracts/biosynthesis , Plant Proteins/genetics , Plant Proteins/metabolism , Proteomics , Sequence Analysis, RNA , Tandem Mass SpectrometryABSTRACT
Recently, an important topic of research has been how climate change is seriously threatening the sustainability of agricultural production. However, there is surprisingly little experimental data regarding how elevated temperature and CO2 will affect the growth of medicinal plants and production of bioactive compounds. Here, we comprehensively analyzed the effects of elevated CO2 and temperature on the photosynthetic process, biomass, total sugars, antioxidant compounds, antioxidant capacity, and bioactive compounds of Gynostemma pentaphyllum. Two different CO2 concentrations [360 and 720µmolmol(-1)] were imposed on plants grown at two different temperature regimes of 23/18 and 28/23°C (day/night) for 60days. Results show that elevated CO2 and temperature significantly increase the biomass, particularly in proportion to inflorescence total dry weight. The chlorophyll content in leaves increased under the elevated temperature and CO2. Further, electron transport rate (ETR), photochemical quenching (qP), actual photochemical quantum yield (Yield), instantaneous photosynthetic rate (Photo), transpiration rate (Trmmol) and stomatal conductance (Cond) also increased to different degrees under elevated CO2 and temperature. Moreover, elevated CO2 increased the level of total sugars and gypenoside A, but decreased the total antioxidant capacity and main antioxidant compounds in different organs of G. pentaphyllum. Accumulation of total phenolics and flavonoids also decreased in leaves, stems, and inflorescences under elevated CO2 and temperature. Overall, our data indicate that the predicted increase in atmospheric temperature and CO2 could improve the biomass of G. pentaphyllum, but they would reduce its health-promoting properties.
Subject(s)
Carbon Dioxide/metabolism , Gynostemma/physiology , Hot Temperature , Photosynthesis , Chlorophyll/metabolism , Climate Change , Gynostemma/growth & development , Plant Leaves/metabolismABSTRACT
ETHNOPHARMACOLOGICAL RELEVANCE: To evaluate the safety of standardized extract of Gynostemma pentaphyllum in rats. MATERIALS AND METHODS: The water extract of Gynostemma pentaphyllum was prepared and standardized, the dry powder yielded 6% gypenosides. In the acute oral toxicity test, the single oral dose of 5000 mg/kg of Gynostemma pentaphyllum extract was given to female Sprague-Dawley rats. In subchronic toxicity test, the oral dose of 1000 mg/kg/day of the extract was given to rats in treatment and satellite groups for 90 days. Satellite groups of both sexes were kept for additional 28 days after 90-day treatment. Control rats received distilled water. RESULTS: Standardized extract of Gynostemma pentaphyllum did not cause death or any toxic signs in rats. The daily administration of the extract for 90 days did not produce lethal or harmful effects. Although certain hematological and blood chemistry values (i.e., neutrophil, monocyte, glucose, and serum alkaline phosphatase levels) were found to be statistically different from the control group, however; these values were within the ranges of normal rats. CONCLUSION: Standardized extract of Gynostemma pentaphyllum did not produce mortality or any abnormality in rats.
Subject(s)
Ethnopharmacology , Gynostemma/chemistry , Plant Extracts/toxicity , Administration, Oral , Animals , Dose-Response Relationship, Drug , Female , Gynostemma/growth & development , Male , Organ Specificity , Plant Components, Aerial/chemistry , Plant Extracts/isolation & purification , Plant Extracts/standards , Rats , Rats, Sprague-Dawley , Thailand , Toxicity Tests, Acute , Toxicity Tests, SubchronicABSTRACT
OBJECTIVE: To distinguish female and male plants of Gynostemma pentaphyllum quickly and accurately in the stage of seedling and to understand the relation between sex differentiation and endogenous plant hormone. METHOD: Stained methods of BTB and enzyme linked immuno-sorbent Assay were used. RESULT: 10 Hours after being dyed, the liquid extract of female plants turned into yellow, while extract of male ones turned green. There were obvious differences on iPAs and GA(1 + 3) contents but no differences on IAA and ABA contents between male and female plants during the stages of seedling and vegetative growth. CONCLUSION: BTB can be used for distinguishing female and male plants and there were a certain relation between sex and endogenous plant hormones.