Sweetpotato (Ipomoea batatas L.) is a globally important food crop that is susceptible to infestation with the root-knot nematode, Meloidogyne incognita, which causes substantial crop losses. Previous transcriptomic and proteomic analyses identified several genes that displayed differential expression patterns in susceptible and resistant cultivars in response to root-knot nematode (RKN) infection. As a result of previous study, RKN infection was confirmed in the RKN-susceptible sweetpotato cultivar Yulmi. Transcriptome analysis confirmed that among the genes that respond in this process, there are many genes related to ethylene biosynthesis. Therefore, in this study, we focused on the ACC oxidase (ACO) gene, the final enzyme of ethylene biosynthesis, and analyzed the expression patterns under various abiotic stress conditions. Using transcriptome data from our previous study, various expression changes in the four ACO genes used in this study were confirmed during RKN infection. The expression of G25011|TU41034 decreased during RKN infection compared to the untreated control, while the expression of G31097|TU51009, G28360|TU46486, and G15447|TU25395 genes increased in the early stages of RKN infection. Expressions of four ACO genes in leaves of sweetpoato were investigated under abiotic stress conditions such as wounding, high salinity, dehydration, and low temperature stress treatment. Expression of the G25011|TU41034 was significantly increased under abiotic stress conditions except low temperature. G31097|TU51009 was hardly expressed under abiotic stress conditions. Although the expression pattern of G28360|TU46486 and G15447|TU25395 was slightly different depending on the type of abiotic stress, an overall increase in expression was observed. It is expected that this study will be used as basic data on how ethylene biosynthesis responds not only to nematode infection but also to various abiotic stress conditions and will be helpful in functional studies of various crops.

The balloon flower (Platycodon grandiflorum A. DC.) is a medicinal and perennial flowering plant. Jangback is an important white-flower type balloon flower cultivar registered in South Korea, but no molecular marker was available to differentiate it from other white-flower lines. Therefore, we evaluated five P. grandiflorum white-flower lines and identified a single nucleotide polymorphism (SNP) derived from the chloroplast TrnL-F genomic sequence that specifically differentiated Jangback from the other four genotypes. Cultivar identification was achieved by detecting allelic variations of the SNP using amplification refractory mutation system-polymerase chain reaction (ARMS-PCR) analysis and high resolution melting (HRM) curve analysis. The present study describes a rapid and reliable method to authenticate the medicinally and economically valuable white-flower Jangback cultivar. Our results indicate that the plastid TrnL-F region provides for marker assisted identification and selection in intraspecific polymorphism studies, thereby the identified SNP marker provides a robust tool along with ARMS-PCR and HRM curve analysis for rapid and efficient identification of the medicinally valuable Jangback cultivar.

Background : Cudrania tricuspidata Bureau is a widely used medicinal perennial woody plant. Obtaining information about the genetic diversity of plant populations is highly important for conservation and germplasm utilization. In this study, we developed single nucleotide polymorphism (SNP) markers derived from chloroplast genomic sequences to identify distinct Korean-specific ecotypes of C. tricuspidata via amplification refractory mutation system (ARMS)-PCR analyses. We performed molecular authentication of twelve C. tricuspidata ecotypes from different regions using DNA sequences in the chloroplast TrnL-F intergenic region. Methods and Results : SNPs were identified based on the results of nucleotide sequence for the intergenic region of TrnL-TrnF gene (chloroplast). Molecular markers were designed for those SNPs with additional mutations on the second base from SNPs for amplification refractory mutation system-polymerase chain reaction (ARMS-PCR). HRM pattern analyses were performed using the Mx3005P QPCR System (Agilent Technologies, CA, USA). Conclusion : We collected 12 individual lines of C. tricuspidata from various region in South Korea and China. Based on the nucleotide sequence in the trnL-trnF intergenic region of these lines, six SNPs and a deletion of 12 bps were identified and 12 individual lines were able to be grouped in one Korean ecotype and two different ecotypes of chinese lines, chinese line 1 and 2. The SNP markers developed in this study are useful for rapidly identifying these specific C. tricuspidata ecotypes collected from different regions.

The effect of salicylic acid(SA) on antioxidant system and protective mechanisms against UV-B induced oxidative stress was investigated in cucumber(Cucumis sativus L.) leaves. UV-B radiation and SA were applied separately or in combination to first leaves of cucumber seedlings, and dry matter accumulation, lipid peroxidation and activities of antioxidant enzymes were measured in both dose and time-dependant manner. UV-B exposure showed reduced levels of fresh weight and dry matter production, whereas SA treatment significantly increased them. SA noticeably recovered the UV-B induced inhibition of biomass production. UV-B stress also affected lipid peroxidation and antioxidant enzyme defense system. Malondialdehyde(MDA), a product of lipid peroxidation, was greatly increased under UV-B stress, showing a significant enhancement of a secondary metabolites, which may have antioxidative properties in cucumber leaves exposed to UV-B radiation. Combined application of UV-B and SA caused a moderate increase in lipid peroxidation. These results suggest that SA may mediate protection against oxidative stress. UV-B exposure significantly increased SOD, APX, and GR activity compared with untreated control plants. Those plants treated with 1.0 mM SA showed a similar pattern of changes in activities of antioxidant enzymes. SA-mediated induction of antioxidant enzyme activity may involve a protective accumulation of H2O2 against UV-B stress. Moreover, their activities were stimulated with a greater increase by UV-B+SA treatment. The UV-B+SA plants always presented higher values than UV-B and SA plants, considering the adverse effects of UV-B on the antioxidant cell system. ABA and JA, second messengers in signaling in response to stresses, showed similar mode of action in UV-B stress, supporting that they may be important in acquired stress tolerance. Based on these results, it can be suggested that SA may participates in the induction of protective mechanisms involved in tolerance to UV-B induced oxidative stress.