Re-examination of the standard cultivation practices of rice in response to climate change in Korea

The impact of climate change has been simulated or estimated to bring about yield decline and quality deterioration of rice in Korea, a temperate country. To cope with these negative impacts, here we propose likely changes in the standard cultivation practices of rice in consideration of the current information on the progress/prediction of climate change and related physiological aspects of rice. Shifting grain-filling period could be a promising choice to optimize temperature for rice grain-filling, a crucial growth stage to productivity, hence providing rice plants with sufficient duration and solar radiation for the period. This choice, however, shortens days to flowering by the additive combined effects of high temperature by delayed transplanting, temperature rise itself by climate change, and accelerated phase change of rice by high temperature and short day-length. These combined effects may delay the time of transplanting in a great extent, hence reducing biomass accumulation of rice before flowering. In these conditions, recovering decreased biomass production is the key concern for rice productivity. This includes raising healthy seedlings by omitting the covering process, dense planting, and nutrient management to enhance plant’s uptake activity. Current standard water management, especially mid-term drainage and intermittent irrigation, would have more importance in the future since they mitigate methane emission from the paddy. Field monitoring for weeds and pests would be an important first step to identify newly developing or thriving species for establishing subsequent controlling strategies. Earlier weed control should be emphasized through adjusting time of herbicide application.     

Evaluation of regional climate scenario data for impact assessment of climate change on rice productivity in Korea

Spatial evaluation of the uncertainty associated with climate data would allow reliable interpretation of simulation results for regional crop yield using gridded climate data as input to a crop growth model. The objective of this study was to examine the spatial uncertainty of regional climate model data through determining optimal seeding date with the ORYZA2000 model for assessment of climate change impact on rice productivity in Korea. The optimal seeding date was determined at each grid point using regional climate model outputs under the RCP 8.5 scenarios. In major rice production areas such as inland plain regions, where temperatures of regional climate data were relatively accurate, the optimal seeding date determined using those gridded data were reasonable. However, areas with complex terrains including areas near bodies of water, e.g. coastal areas, riverbasins, lakes, and mountainous areas, had a relatively large uncertainty of the optimal seeding date determined using the regional climate data. These results indicated that the uncertainty of regional climate data at a high spatial resolution of 12.5 km should be taken into account in the regional impact assessment based on crop growth simulations in Korea. In addition, further studies would be merited to assess the impact of climate change on rice yield at an ultra-high spatial resolution of 1 km in Korea. Crop yields were projected to decrease after the 2020s when crop yield simulations from inland plain areas were considered, which suggested that adaptation strategies should be established and implemented in the near future.     

Antioxidant activity and inhibition of lipid peroxidation in germinating seeds of transgenic soybean expressing OsHGGT

Tocochromanols are potent lipid-soluble antioxidants and essential nutrients for human health. Genetic engineering techniques were used to develop soybeans with enhanced vitamin E levels, including tocotrienols, which are not found in soybean. The gene encoding rice homogentisate geranylgeranyl transferase (HGGT) was overexpressed in soybeans using seed-specific and constitutive promoters. The association between abundance of vitamin E isomers and antioxidant activity was investigated during seed germination. With the exception of β-tocotrienol, all vitamin E isomers were detected in germinating seeds expressing OsHGGT. The antioxidant properties of germinating seed extracts were determined using 1,1-diphenyl-2-picrylhydrazyl (DPPH) and 2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) radicals and lipid peroxidation (TBARS). Compared with intact wild-type seeds, transgenic seeds showed increases in radical scavenging of 5.4-17 and 23.2-35.3% in the DPPH and ABTS assays, respectively. Furthermore, the lipid peroxidation levels were 2.0-4.5-fold lower in germinating seeds from transgenic lines than in wild-type seeds. Therefore, it appears that the antioxidant potential of transgenic oil-producing plants such as soybean, sunflower, and corn may be enhanced by overexpressing OsHGGT during seed germination.     

Effect of Aspergillus oryzae-challenged germination on soybean isoflavone content and antioxidant activity

Application of microbial stress to soybean during germination induces the accumulation of phytoalexins, which have many health benefits. In this study, the effects of stress induced by Aspergillus oryzae on the phytochemical composition of germinating soybeans were investigated, and their radical scavenging activity was compared with those of ungerminated (US) and germinated (GS) soybeans. Additionally, the antioxidant activity of coumestrol, a soybean phytoalexin, against hydrogen peroxide-induced reactive oxygen species (ROS) was investigated in HepG2 cells. A. oryzae exposure significantly decreased the total isoflavone content and induced coumestrol and glyceollin I. A. oryzae-challenged germinated soybeans exhibited the highest radical scavenging activity (IC(50) = 0.55 mg/mL) as compared to US and GS. Coumestrol exhibited significantly higher radical scavenging activity than daidzein and genistein. Furthermore, coumestrol significantly prevented hydrogen peroxide-induced ROS production and lipid peroxidation and inhibited decreases in cell viability, intracellular glutathione (GSH) levels, and superoxide dismutase (SOD) activity. These results indicate that using food-grade A. oryzae to elicit the biosynthesis of phytoalexins alters the secondary metabolite profiles of the soybeans and offers enhanced bioactivity of soybean as a functional food ingredient.     

Metabolite profiling of Angelica gigas from different geographical origins using 1H NMR and UPLC-MS analyses

Angelica gigas obtained from different geographical regions was characterized using (1)H nuclear magnetic resonance (NMR) spectroscopy and ultraperformance liquid chromatography-mass spectrometry (UPLC-MS) followed by multivariate data analyses. Principal component analysis (PCA) and orthogonal partial least-squares-discriminant analysis (OPLS-DA) score plots from (1)H NMR and UPLC-MS data sets showed a clear distinction among A. gigas from three different regions in Korea. The major metabolites that contributed to the discrimination factor were primary metabolites including acetate, choline, citrate, 1,3-dimethylurate, fumarate, glucose, histamine, lactose, malate, N-acetylglutamate, succinate, and valine and secondary metabolites including decursin, decursinol, nodakenin, marmesin, 7-hydroxy-6-(2R-hydroxy-3-methylbut-3-ethyl)coumarin in A. gigas roots. The results demonstrate that (1)H NMR and UPLC-MS-based metabolic profiling coupled with chemometric analysis can be used to discriminate the geographical origins of various herbal medicines and to identify primary and secondary metabolites responsible for discrimination.     

Production of conjugated linoleic acid (CLA) by Bifidobacterium breve LMC520 and its compatibility with CLA-producing rumen bacteria

This study was performed to characterize the ability of an active Bifidobacterium strain to produce conjugated linoleic acid (CLA) and to test its possible utilization as a probiotic compatible to the ruminal condition. Bifidobacterium breve LMC520 can actively convert linoleic acid (LA) to cis-9,trans-11-CLA, which is a major isomer derived from microbial conversion. LMC520 showed reasonable tolerance under acidic conditions (pH 2.5 with 1% pepsin) and in the presence of oxgall (0-3%). The growth and CLA production of LMC520 were tested under ruminal conditions and compared with those of Butyrivibrio fibrisolvens A38, which is a major CLA producer in the rumen as an intermediate in the biohydrogenation (BH) process. LMC520 converted 15% of LA to CLA under ruminal conditions, which was 2 times higher activity than that of A38, and there was no decline in CLA level during prolonged incubation of 48 h. The BH activity of LMC520 was comparable to that of A38. When LMC520 was cocultured with A38, even with slight decrease of CLA due to high BH activity by A38, but the level of CLA was maintained by the high CLA-producing activity of LMC520. This comparative study shows the potential of this strain to be applied as a functional probiotic not only for humans but also for ruminants as well as to increase CLA production.     

Sesquiterpenoids isolated from the flower buds of Tussilago farfara L. inhibit diacylglycerol acyltransferase

Inhibition of acyl CoA:diacylglycerol acyltransferase (DGAT), which is a key enzyme in triglyceride synthesis in eukaryotic organisms, has been proposed as one of the drug targets for treating obesity, type II diabetes mellitus, and metabolic syndrome. Bioassay-guided fractionation of EtOH extract of the flower buds of Tussilago farfara , using an in vitro DGAT enzyme assay, resulted in the isolation of four known sesquiterpenoids, tussilagonone (1), tussilagone (2), 7beta-(3-ethyl-cis-crotonoyloxy)-1alpha-(2-methylbutyryloxy)-3,14-dehydro-Z-notonipetranone (3), and 8-angeloylxy-3,4-epoxy-bisabola-7(14),10-dien-2-one (4). DGAT1 inhibitory activity was studied by in vitro DGAT assay using rat liver microsomes and HepG2 cell microsomes. They showed DGAT1 inhibition with IC(50) values of 99.2 (1), 18.8 (2), 47.0 (3), and 211.1 (4) microM (for rat liver microsomes) and >1 mM (1), 49.1 (2), 160.7 (3), and 294.4 (4) microM (for HepG2 cell microsomes), respectively. Compound 2 showed the most potent inhibition against microsomal DGAT1 derived from rat liver and human hepatocellular carcinoma HepG2 cells and also significantly inhibited triglyceride synthesis by suppressing incorporation of [(14)C]acetate or [(14)C]glycerol into triglycerides in HepG2 cells. These findings suggest that tussilagone is a potential lead compound in the treatment of obesity and type 2 diabetes.     

Influence of varied soil microbial and inorganic nutrient conditions on the growth and vesicular-arbuscular mycorrhizal colonization of little bluestem [Schizachyrium scoparium (Michx.) Nash]

Summary A difference in biomass production between plants grown in autoclaved soil and non-autoclaved soil under N and base (Ca + Mg) treatments was probably caused by soil microbes other than vesicular-arbuscular mycorrhizal fungi. The plants were grown for 70 days in autoclaved soil, autoclaved soil with a vesicular-arbuscular mycorrhizal-free filtrate of non-autoclaved soil added, and non-autoclaved soil. The plants in each substrate received additional N, P, or Ca + Mg (base treatment) weekly. Control plants received no additional nutrients. The plant response to various substrates was a function of nutrient treatment. Colonization of roots by vesicular-arbuscular mycorrhizal fungi in non-autoclaved soil was lowest with the N and P treatments. There were significant negative correlations between vesicular-arbuscular mycorrhizal colonization and all plant growth variates. For all nutrient treatments, there were no differences in total biomass between plants grown in non-autoclaved soil and in the autoclaved-plus-filtrate substrate.     

猪苓的人工培养条件研究

猪苓的白色长菌丝在PDA培养基上能够形成厚实可剥的菌丝块。猪苓生长菌丝可形成锁状联结、顶端膨大,菌丝真径0.95～2.80um,适宜生长条件为20℃、pH4。振荡培养下,形成15～20um大小的菌丝块,颜色如潜伏其菌核的灰黄色。在6种生长原木上,猪苓形成菌丝块大小为3～5um。在PDA培养基上猪苓与蜜环菌混合培养比单独培养的菌丝粗,菌丝密度大,在原木上,猪苓菌丝与蜜环菌菌丝形成共生联结,同时在与蜜环菌紧连的菌丝块边缘,有多点状的自我防御结构。木质素降解活性检测表明,4个菌株中的A、B、C使澳酚蓝脱色后的吸光度为0.0635～0.0902,而菌株D的活性可以忽略。