Nugroho Nofriarno, B. Daryono, Avia Purnama Saputri, Estiyani Indraningsih
{"title":"ANALISIS FENOTIPE DAN PLOIDI TANAMAN MELON (Cucumis melo L.) HASIL PERLAKUAN EKSTRAK ETANOLIK DAUN TAPAK DARA (Catharanthus roseus [L] G. Don.)","authors":"Nugroho Nofriarno, B. Daryono, Avia Purnama Saputri, Estiyani Indraningsih","doi":"10.19109/BIOTA.V4I2.2061","DOIUrl":null,"url":null,"abstract":"Anti-mitotic agents such as colchicine have been used to induce polyploidy in various plants. On the other hand, vincristine and vinblastine are also antimitotic agent extracted from Periwincle (Catharanthus roseus [L] G. Don) were previously studied to produce autotetraploid on shallot tuber (Allium cepa L.). Therefore, in this study phenotype character and ploidy of muskmelon (Cucumis melo L.) produced by etanolic extract of periwikle leaves were determined. The effects of different concentration of etanolic extract of periwinkle leaves on polyploidy induction in muskmelon were examined. Melon seedling of two days old were immersed in 0.5%, 0.1%, and 0.05% for 8 hours. Then seedling was grown on the polybag and a drop of each concentration of periwinkle leaves’s etanolic extract was added into apical shoot. Melon seedling of ten days old were moved and cultivated and harvested on 60 days after cultivation. Phenotypic character such as: plant high, stem diameter, leaf area, fruit weight, fruit area around, flesh fruit thickness, skin fruit thickness, fruit horizontal diameter, fruit, vertical diameter, number of seeds, weight of 100 gram of seed, seed leght, seed width, and seed thickness were examined. The ploidy degree was determined by count of chromosome number root tips of second generation muskmelon sprout. Result of this study revealed that 0.05% etanolic extract of periwinkle leaves for 8 hours immersed is optimum concentration to induce autotetraploid muskmelon (4n=48). Autotetraploid phenotypic character of muskmelon produced by 0.05% etanolic extract of periwinkle leaves were generally bigger than control plants statistically significant in stem diameter, leaf area, and fruit horizontal diameter. The result also showed that the chromosome number of second generation autotetraploid muskmelon sprout was tetraploid (4n=48).","PeriodicalId":31624,"journal":{"name":"Jurnal Biota","volume":"89 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Jurnal Biota","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.19109/BIOTA.V4I2.2061","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
摘要
抗有丝分裂剂如秋水仙碱已被用于多种植物的多倍体诱导。另一方面,长春新碱和长春碱也是从长春花(Catharanthus roseus [L] G. Don)中提取的抗有丝分裂剂,在葱块茎(Allium cepa L.)上产生同源四倍体。因此,本研究测定了以甜瓜叶乙醇提取物为原料的甜瓜(Cucumis melo L.)的表型和倍性。研究了不同浓度长春花叶乙醇提取物对甜瓜多倍体诱导的影响。2日龄甜瓜幼苗分别在0.5%、0.1%和0.05%的培养基中浸泡8小时。然后在塑料袋上育苗,在顶芽中加入不同浓度的长春花叶乙醇提取物各一滴。10天大的瓜苗移栽,栽培后60天收获。检测了株高、茎粗、叶面积、果重、果周面积、果肉厚度、果皮厚度、果横径、果纵径、种子数、百克种子重、种子轻、种子宽、种子厚等表型性状。通过对二代甜瓜芽苗根尖染色体数目的计数来确定其倍性程度。结果表明,0.05%的长春花叶乙醇提取物浸泡8小时是诱导同源四倍体甜瓜的最佳浓度(4n=48)。0.05%长春花叶乙醇提取物所产甜瓜的同种四倍体表型性状在茎粗、叶面积和果实横径上均大于对照植株,具有统计学意义。结果还表明,第二代同源四倍体甜瓜芽的染色体数目为四倍体(4n=48)。
ANALISIS FENOTIPE DAN PLOIDI TANAMAN MELON (Cucumis melo L.) HASIL PERLAKUAN EKSTRAK ETANOLIK DAUN TAPAK DARA (Catharanthus roseus [L] G. Don.)
Anti-mitotic agents such as colchicine have been used to induce polyploidy in various plants. On the other hand, vincristine and vinblastine are also antimitotic agent extracted from Periwincle (Catharanthus roseus [L] G. Don) were previously studied to produce autotetraploid on shallot tuber (Allium cepa L.). Therefore, in this study phenotype character and ploidy of muskmelon (Cucumis melo L.) produced by etanolic extract of periwikle leaves were determined. The effects of different concentration of etanolic extract of periwinkle leaves on polyploidy induction in muskmelon were examined. Melon seedling of two days old were immersed in 0.5%, 0.1%, and 0.05% for 8 hours. Then seedling was grown on the polybag and a drop of each concentration of periwinkle leaves’s etanolic extract was added into apical shoot. Melon seedling of ten days old were moved and cultivated and harvested on 60 days after cultivation. Phenotypic character such as: plant high, stem diameter, leaf area, fruit weight, fruit area around, flesh fruit thickness, skin fruit thickness, fruit horizontal diameter, fruit, vertical diameter, number of seeds, weight of 100 gram of seed, seed leght, seed width, and seed thickness were examined. The ploidy degree was determined by count of chromosome number root tips of second generation muskmelon sprout. Result of this study revealed that 0.05% etanolic extract of periwinkle leaves for 8 hours immersed is optimum concentration to induce autotetraploid muskmelon (4n=48). Autotetraploid phenotypic character of muskmelon produced by 0.05% etanolic extract of periwinkle leaves were generally bigger than control plants statistically significant in stem diameter, leaf area, and fruit horizontal diameter. The result also showed that the chromosome number of second generation autotetraploid muskmelon sprout was tetraploid (4n=48).