본 연구는 과육색이 노란 국내 육성 키위 ‘Jecy Gold’ 품종의 수확 적기 판정과 후숙 후 당도 예측 방법을 개발하고자 수행하였다. 과실 생육 단계 중 과실 비대기는 BBCH 70~78(DAA 10~110), 과실 성숙 단계는 BBCH 80(DDA 140), 당도가 급격히 증가하는 시기는 BBCH 83(DDA 160), 과육이 부드러워지는 시기는 BBCH 87(DAA 190), 과실이 노화되는 시기는 BBCH 90(DDA 210)이었다. 이러한 결과를 토대로 BBCH 83(DAA 160일)에서 수확하는 것이 가장 바람직할 것으로 판단되었다. 후숙 전 과실 건물률과 후숙 후 당도가 정의 상관관계를 보였다. 후숙 전 건물률을 이용하여 후숙 후 당도를 예측하기 위하여 회귀분석을 수행한 결과, 후숙 후 당도(y)=1.1841ⅹ건물율(x)-3.5244(r²=0.9338)으로 나타났으며, 실측 값과 예측 값을 이용하여 회귀분석을 수행한 결과, 상관계수 R² 값이 0.86으로 높게 나타났다. 따라서 수확 시기의 건물률을 이용하면 후숙 후 당도를 추정할 수 있을 것으로 판단된다.

In Korea, 1,212 accessions of garlic are conserved in Namhae, Jeonju, Danyang and Muan with IT (Identity) number. This study was carried out to evaluate characteristics of 163 garlic cultivars conserved in Namhae branch, NIHHS, RDA and search valuable genetic resources for breeding. In horticultural characteristics, there was wide variation for bulb weight, clove weight and clove number per bulb with large coefficient of variation (CV) 40.04%, 43.98% and 39.64% respectively. Alliin content analyzed by HPLC was 16.75±6.22mg·g-1 DW (Dry weight) and had 37.16% CV. The highest alliin content was 32.27mg·g-1 in Local5. In correlation analysis, there were a strong positive correlation between bulb weight and bulb diameter and a non-correlation between clove number per bulb and bulb weight, height and diameter. Major characters included in the principal components were bulb weight, bulb height, bulb diameter, plant height, clove number per bulb, leaf sheath diameter and alliin content. According to characteristics of garlic, 163 germplasms were clustered into 10 groups. In total 10 clusters, the average bulb weight is the heaviest at 5th cluster and average alliin content is the highest at 4th cluster. These clusters will be used for selection breeding program to cultivate garlic that has heavier weight and high alliin content.

This study was conducted to investigate the effects of various mulching materials on growth and yield of okra (Abelmoschus esculentus L. Moench). Three kinds of polyethylene (PE) mulching materials were used which are: black (Black), green (Green), and white and black on both sides (White), black non-woven fabric (Fabric), and barley straw (Straw) and the control plot (Control) were also used in this study. The change of soil temperature was observed in various mulching materials with Green showing the highest average temperature of 24.4o, followed by Black > Fabric > Control > White > Straw. The variation of plant length,, aboveground weight, and root weight were constant in the order of Green > Black > White > Fabric > Control > Straw. Total yield (number of fruits) were 281,000 in Green which was the highest yield, and the least was from Straw which was 62.3% of Green. Total weight of fruits in Green was 395 kg which was the heaviest, and in Straw was least with 226 kg Hence, the weight of fruits

망고는 호광성 작물로써 많은 광을 필요하나 대부분의 농가에서는 하우스 내 밀식재배를 하기 때문에 수관내부의 광이 부족하여 생육이 잘 이루어지지 않고 과실의 착색 및 품질이 떨어지고 있다. 따라서 본 연구는 망고 하우스 내 토양에 다공질필름을 피복하여 수관하부의 광 환경을 개선하여 과실 품질 및 착색을 향상 시키며, 생육 시기별 피복 시기를 달리 하여 생육 별 피복 처리의 효과를 구명하고자 수행되었다. 1. 다공질필름 피복 처리 효과 1) 다공질필름 피복에 대한 광반사율은 대조구에 비해 처리구가 높았다. 2) 과중 및 가용성 고형물 함량의 변화에는 대조구에 비해 처리구가 높게 나타났으며 산 함량에는 유의 차가 인정되지 않았다. 3) 과피의 착색 정도에는 피복 처리가 대조구에 비해 착색이 잘 되었다. 2. 다공질필름 피복 시기별 처리 효과 1) 만개 후 5일부터 피복 처리를 했을 경우가 과중 및 가용성 고성물 함량이 높게 나타났으며, 산함량 및 과피의 착색정도에는 유의차가 인정되지 않았다. 2) 과실의 유리당 함량은 sucrose, fructose, glucose 순으로 많았으며, sucrose는 가용성 고형물 함량과 마찬가지로 만개 후 5일부터 피복했을 경우 높게 나타났다. 3)피복 시기에 따른 유기산 함량의 변화에는 유의차가 인정되지 않았다.

아티초크는 가을에 정식하여 겨울철 월동 중에 화아분화가 이듬해 5월경에 수확이 가능하다. 본 시험은 아티초크 육묘 중 저온처리를 하여 생산시기를 7월로 늦추고자 수행하였다. 시험품종은 ‘그린글로브’ 및 ‘임페리얼스타’를 이용하였다. 파종은 72공 플러그 트레이를 이용하여 2월 10일에 파종하였고 4주간 17oC에서 육묘한 후 3, 6, 9, 12oC에서 4주간 육묘하였으며 4월 8일에 노지 포장에 정식하였다. 재식거리는 이랑폭 150cm에 주간거리 50cm(1,523주/10a), 1조식으로 하였다. 온도 처리별로는 6oC 처리에서 화뢰 발생이 63%로 가장 많았고 12oC에서는 33%로 가장 낮았으며 무처리의 경우는 5%의 화뢰가 형성되어 저온에 민감한 품종임을 알 수 있었다. ‘그린글로브’ 품종의 경우 9oC에서 화뢰 형성율이 가장 높아 28%였고 12oC에서는 10%로 가장 낮았으며 무처리의 경우는 화뢰가 전혀 형성되지 않았다. 화뢰중은 ‘임페리얼스타’ 품종이 97g 내외였고 ‘그린글로브’ 86g 내외로 자랐다. 수량은 ‘임페리얼스타’에서 215kg, ‘그린글로브’에서는 108kg을 보였다.

제주지역 참다래 과원의 영양진단을 통해 참다래 수체 내 영양상태를 파악하여 시비기 준을 설정하기 위해 제주지역의 참다래 과원 110 곳의 토양과 참다래 잎을 조사하였다. 참다래 수체의 영양진단을 위한 엽채취 시기는 엽내 성분 함량이 가장 안정된 시기인 7 월 중순~8월초가 가장 적당하였다. 참다래 엽내 무기성분 평균함량은 질소 2.74, 인산 0.20, 칼륨 1.91, 칼슘 1.91, 마그네슘 0.51% ,철 147.0, 망간 160.1, 아연 54.0mg/kg 이었다. 엽내 무기성분 함량의 예상 임계치를 설정하여 정상 범위를 구한 결과, 질소는 2.5~3.0, 인산은 0.16~ 0.24, 칼륨은 1.80~2.44, 칼슘은 1.95~2.63, 마그네슘은 0.39~0.63%였다. 제주지역 참다래원 토양의 이화학성은 pH 5.46, 유기물 9.69%, 유효 인산 220.7 mg/kg, 치환성 칼륨 1.1, 칼슘 4.1, 마그네슘 1.48 c㏖/kg, 양이온 치환용 량 16.18 c㏖c/kg이었다.

Background: In the herbal medicinal industry, Angelica gigas Nakai, Angelica sinensis (Oliv.) Diels. and Angelica acutiloba (Siebold & Zucc.) Kitag. are often confused, because the roots of the three species can not be distinguished by their appearance. This confusion can cause serious side effects. In this study, we determined the origins of Angelica roots distributed in the Korean market using the simple sequence repeat (SSR) markers developed based on the A. gigas chloroplast DNA sequence. Methods and Results: We collected twenty seven A. gigas and three A. acutiloba samples from the Seoul, Daegu, and Cheongju herbal medicinal markets. Fifty sections of one collection were mixed and ground to make a powder, which was used for DNA extraction using the cetyl trimethylammonium bromide (CTAB) method. Chloroplast based SSR markers were applied to the DNA for the determination of the species. In addition, polymorphism was found in eight samples. The phylogenetic analysis showed that the A. gigas roots collected from herbal medicinal markets were clearly discriminated from A. sinensis and A. acutiloba even though they were grouped into four clusters. Conclusions: This study showed that chloroplast based SSR markers would help the discrimination of Angelica roots in the Korean herbal medicinal industry and the markers are useful to prevent confusion between Angelica roots.

Background : Codonopsis lanceolata is a perennial plant of Campanulaceae and mainly distributed in East Asia such as Korea, China, and Japan. C. lanceolata has a unique taste and aroma, and it is rich in minerals such as phosphorus and calcium, and vitamin B1 and B2, so our ancestors used the plant as medicinal herb and edible vegetable. However, systematic cultivation and development of varieties have not been achieved compared to demand or high added value. The genetic diversity and relationship analysis of the plants help to increase the efficiency of breeding through genetic variation. Methods and Results : Ten species of Codonopsis plants were used as materials and DNA was extracted from each 4 individuals per species and quantified at a concentration of 10 ng /㎕. The extracted DNA was pooled by species and PCR was performed using the EST-SSR marker developed based on C. lanceolata in the previous study. PCR amplification was carried out using a denaturation at 94℃ for 30 sec, annealing at 58℃ for 30 sec and extension at 72℃ for 30 sec, repeated for 35 total cycles. The PCR products were separated in a 4% agarose gell at 100 V for 40 min. Conclusion : In this study, C. lanceolata collections was determined among several Codonopsis species using these molecular marker. It is expected that the data of this study can be used as reference for genetic polymorphism analysis and related gene studies of Codonopsis species.

Background : Codonopsis lanceolata is a perennial plant of Campanulaceae with characteristic flavor and aroma and this plant has saponin, flavonoid, and inulin, which are reported to have physiological activity and antioxidant activity. In contrast, breeding or study of C. lanceolata varieties had not been done for a long time. Genetic polymorphism and phylogenetic relationship analysis of the plants by region of the crops can help the collection of genetic backgroud data for variety development. Methods and Results : In this study, we collected 26 C. lanceolata lines (95 individual plants) from 26 regions in Korea. We genotyped the collected lines using SSR markers developed in the previous study and analyzed the population structure based on the results. Population structures were analyzed using model-based STRUCTURE software (version 2.3.4) using the following parameters: Number of clusters (K) set = 1 to 12; Number of Iterations = 5; Length of Burning Period = 100,000; Number of MCMC (Markov Chain Monte Carlo) Reps after Burnin = 100,000. As a result, Of the 26 collections, were genetically grouped into 6 or 7 groups. Conclusion : The 26 C. lanceolata collections (95 individual plants) were genetically grouped but not grouped by collected regions. These results suggest that C. lanceolata has diverse genetic backgrounds and this data could be used as a basis for genetic polymorphism analysis of Codonopsis species.

Background: Rehmannia glutinosa is a perennial herb belonging to the family Scrophulariaceae. Its root has been utilized as a traditional medicine but the aerial parts (flower, flower stalk, leaf) are not used. We aimed to determine the content of three compounds [aucubin, catalpol, and γ-aminobutyric acid (GABA)] in the different organs of R. glutinosa cultivars (Dakang, Tokang, and Suwon 9) Methods and Results: The flower, flower stalk, leaf, and root of R. glutinosa were harvested at the end of August. The aucubin and catalpol contents were analyzed by LC/MS, whereas the GABA content was analyzed by GC/MS. The aucubin content was the highest in the leaf, while catalpol and GABA were the highest in the flower. The aucubin contents of leaf in Dakang, Tokang, and Suwon 9 were 1.43, 0.81, and 1.07㎎/g, respectively. The catalpol contents of flower in Dakang, Tokang, and Suwon 9 were 41.06, 28.78, and 37.48㎎/g, respectively, the GABA contents were 0.79, 0.76, and 0.65㎎/g, respectively. Conclusions: The aucubin, catalpol, and GABA contents were higher in the leaf and flower than that in the root. This study show that R. glutinosa leaf and flower can be used as a potential supplement.

Background : Platycodon grandiflorum has been used as food material and a traditional medicine in Korea. In order to develop an efficient in vitro micropropagation technique for a rare plant species and conservation for inbred line of plant breeding. Methods and Results : Plant regeneration via organogenesis and somatic embryogenesis was investigated in Platycodon grandiflorum. Leaf, stem, root tissues of 7-day-old seedlings were cultured on 1/2MS medium containing various concentration (0, 0.5, 1 and 2 ㎎/L) of IBA, BA and NAA. The results showed that 1/2MS medium supplemented with BA+NAA 2.0 ㎎/L yielded the highest callus formation ratio of 73.5%. When various tissues (leaf, stem, root) were tested on 1/2MS medium containing BA 2.0 ㎎/L+ NAA 2.0 ㎎/L for somatic embryogenesis, the optimum tissue for embryogenic shoot induction was stem tissue. Callus were cultured on MS medium containing various concentration (0, 0.5 and 1 ㎎/L) of BA and NAA. The best rooting rate was achieved by three different medium (B5, 1/2MS and MS) and 1/2MS medium cultured the highest rooting ratio (82%). Conclusion : This study suggested that above micropropagation techniques can be used for rapid multiplication as well as in vitro or in vivo conservation of the Platycodon species.

Background : Codonopsis lanceolata is a flowering perennial climber. The roots are used as medicinal materials or vegetables. C. lanceolata is distributed in India and East Asia such as China, Japan as well as Korea. Recently, demand for C. lanceolata is increasing as a healthy food. In South Korea, this plant is widely cultivated in Gangwon-do province. Although, C. lanceolata is one of the most important medicinal plants in Korea, an elite, inbred line or a variety has not been developed yet. Simple sequence repeat (SSR) marker is a powerful tool for analysis of genetic relationships. In addition, it is a useful tool for studying the non-reference plant genome, due to its even distribution throughout the genome, as well as its high polymorphism between individuals. Methods and Results : We constructed microsatellite-enrichment libraries using C. lanceolata genomic DNA, and obtained a total of 226 non-redundant contig sequences. Routine PCR was performed using gDNA as templates for the polymorphic markers screening. Finally, total 15 polymorphic SSR markers based on C. lanceolata genomic sequences were successfully developed. These markers were applied to 53 C. lanceolata collected from Korea. 103 alleles of the 15 SSR markers ranged from 3 to 19 alleles at each locus, with an average of 6.87. The average of observed heterozygosity and genetic diversity were 0.42 and 0.62, respectively. The average of polymorphism information content (PIC) value was 0.57. The genetic distance value ranged from 0.73 to 0.93, and there was no observed distinct group according to the collecting areas. Conclusion : We developed 15 novel SSR markers from C. lanceolata genomic sequences for further genetic studies. Also, we concluded that the lineage of C. lanceolata collected in Korea has not been established systematically.

Background : In the herbal medicine market, Angelica gigas, Angelica sinensis, and Angelica acutiloba are all called "Danggui" and used confusingly. We aimed to assess the genetic diversity and relationships among 14 Angelica species collected from different global seed companies. Toward this aim we developed DNA markers to differentiate the Angelica species. Methods and Results : A total of 14 Angelica species, A. gigas, A. acutiloba, A. sinensis, A. pachycarpa, A. hendersonii, A. arguta, A. keiskei, A. atropurpurea, A. dahurica, A. genuflexa, A. tenuissima, A. archangelica, A. taiwaniana, and A. hispanica were collected. The genetic diversity of all 14 species was analyzed by using five chloroplast DNA-based simple sequence repeat (SSR) markers and employing the DNA fragment analysis method. Each primer amplified 3 - 12 bands, with an average of 6.6 bands. Based on the genetic diversity analysis, these species were classified into specific species groups. The cluster dendrogram showed that the similarity coefficients ranged from 0.77 to 1.00. Conclusions : These findings could be used for further research on cultivar development by using molecular breeding techniques and for conservation of the genetic diversity of Angelica species. The analysis of polymorphic SSRs could provide an important experimental tool for examining a range of issues in plant genetics.

Background : Platycodon grandiflorum is a perennial plant and a member of Campanulaceae family. Since ancient times, they have been using P. grandiflorum as an important medicinal plant in Korea. Platycodin D is the most abundant saponin derived from P. grandiflorum and pharmacologically active component. Cytochrome P450s (CYPs) are important enzymes in the saponin biosynthesis. CYP is, in general, the terminal oxidase enzymes and essential roles in saponin biosynthesis pathway by hydroxylation or oxidaition of triterpene skeletons. Methods and Results : We tried to identify CYP genes related to saponin biosynthesis of P. grandiflorum through RNA-seq analysis. The sequencing was performed using Illumina Hi-Seq platform after cDNA library preparation. The produced reads were assembled using CLC Genomics Workbench software (CLC Bio, Inc.). We obtained 122,663 contigs and found 191 putative CYP genes. Familes of CYP716, CYP708, CYP93 and CYP51 were selected as putative saponin biosynthesis related gene families using phylogenetic relationship analysis. Conclusion : The results in this study could help to find the CYPs related to saponin biosynthesis pathway of P. grandiflorum.

Background : Chrysanthemum indicum L. is used in medicine, for bee, ornamental as multivoltinism plant resources. The purpose of this study was to evaluate methods of rooting promotion to make high quality medicinal plants, thereby increasing farm income. This study investigated the effects of different cuttage period, extraction site, shading degree, nursery tray for promoting cutting slips rooting in Chrysanthemum indicum L. Methods and Results : It is used New variety "Gamkuk 1" that were forstered in Gyeongsangnam-do Agricultural Research & Extension Services. Method of application with cuttage period were conducted under five condition; Around the middle of April, Toward the end of April, Early in May, Around the middle of May, Toward the end of May. Early in May plant length was longer than other cuttage period as 41.2%, 83.7% and are significant at significance level 0.05. Method of application with extraction site were conducted under three condition; 1 - 3 node, 4 - 6 node, 7 - 9 node. Leaf number in 1 - 3 node was more than other extration site as 19.4%, 33.6%. Also root length in 1 - 3 was more than other extration site as 10.5%, 23.2%. Method of application with shading degree were conducted under three condition; 50%, 70%, 90%. Plant length in 50 - 70% was longer than 90% shading degree as 23.8%, 24.2%. Also shading degree 50 - 70% had many root length and root number. Method of application with nursery tray were conducted under five condition; 72, 105, 128, 162, 200 tray. Plant length in 105, 128 tray was longer as 8.5 - 35.3% than other nursery tray and are significant at significance level 0.05. Conclusion : According to the results, Early in May, extraction site 1 - 3 node, shading degree 50 - 70%, nusery tray 105, 128 showed the highest growth on cutting slips root promotion in Chrysanthemum indicum L.

Background : Medicinal crop has been used in the traditional Asian medicinal methods. From ancient times, various kinds of medicinal crop are being cultivated in East Aisa including Korea, China and Japan. In Korea, they used a variety of medicinal plants in folk medicine and oriental medicine since ancient times. Molecular markers can be widely used in a variety of settings such as effective-loci estimation, genetic-diversity characterization, allelic-effect studies, gene-flow studies, quantitative-trait locus (QTL) mapping, and evolutionary studies. The genetic analyses of crops require large numbers of useful molecular markers for genetic or QTL identification, comparative mapping and breeding. Studying the genetic diversity and genetic relationship of crops can assist breeders. Crop genetics within a breeding program enable the economic and effective cultivar development. We tried to develop a variety of molecular markers from Angelica gigas genomic sequences for genetic studies and breeding. Methods and Results : A. gigas resources cultivated in Republic of Korea were collected. Fresh leaves were ground with liquid nitrogen and gDNA was extracted using a DNeasy Plant Mini kit (Qiagen, Valencia, CA, USA). We sequenced the whole genomes of five A. gigas accessions using Illumina HiSeq 2500 platform and identified genomic Simple Sequence Repeat (SSR) and InDel markers. DNA amplification was conducted using the PCR system (Bio-Rad T-100 Thermal Cycler). PCR products were separated by capillary electrophoresis on the ABI 3730 DNA analyzer (Applied Biosystems) and Fragment analyzer automated CE system (Advanced Analytical Technologies, Ankeny, IA, USA). Conclusion : We developed novel SSR and InDel markers from A. gigas genomic sequences for further genetic studies and breeding.

Background: In the herbal medicine market, Angelica gigas, Angelica sinensis, and Angelica acutiloba are all called "Danggui" and used confusingly. We aimed to assess the genetic diversity and relationships among 14 Angelica species collected from different global seed companies. Toward this aim we developed DNA markers to differentiate the Angelica species. Methods and Results: A total of 14 Angelica species, A. gigas, A. acutiloba, A. sinensis, A. pachycarpa, A. hendersonii, A. arguta, A. keiskei, A. atropurpurea, A. dahurica, A. genuflexa, A. tenuissima, A. archangelica, A. taiwaniana, and A. hispanica were collected. The genetic diversity of all 14 species was analyzed by using five chloroplast DNA-based simple sequence repeat (SSR) markers and employing the DNA fragment analysis method. Each primer amplified 3 - 12 bands, with an average of 6.6 bands. Based on the genetic diversity analysis, these species were classified into specific species groups. The cluster dendrogram showed that the similarity coefficients ranged from 0.77 to 1.00. Conclusions: These findings could be used for further research on cultivar development by using molecular breeding techniques and for conservation of the genetic diversity of Angelica species. The analysis of polymorphic SSRs could provide an important experimental tool for examining a range of issues in plant genetics.

Background : Platycodon grandiflorum is a perennial plant and a member of Camanulaceae family. Since ancient times, they have been using P. grandiflorum as an important medicinal plant in Korea. Platycodin D is the most abundant saponin derived from P. grandiflorum and pharmacologically active component. UDP-glycosyltransferases (UGTs) are important enzymes in the saponin biosynthesis. UGT is a glycosyltransferase and act on the final step of the secondary metabolite biosynthesis. Methods and Results : We tried to identify UGT genes related to saponin biosynthesis of P. grandiflorum through RNA-seq analysis. The sequencing was performed using Illumina Hi-Seq platform after cDNA library preparation. The produced reads were assembled using CLC Genomics Workbench software (CLC Bio, Inc.). We obtained 122,663 contigs and found 137 putative UGT genes. Familes of UGT71, UGT73, and UGT74 were selected as putative saponin biosynthesis related gene families using phylogenetic relationship analysis. qPCR condition about UGT73 is preheating 94℃ 180 sec, denaturation 94℃ 60 sec, annealing 53℃ 60 sec, extension 72℃ 90 sec, final extension 72℃ 600 sec, 45 cycles repeated. Conclusion : The results in this study could help to find the UGTs related to saponin biosynthesis pathway of P. grandiflorum.