{"title":"Somatic Embryogenesis and Plant Regeneration from Mature Zygotic Embryos of Red Spruce","authors":"I. Harry, T. Thorpe","doi":"10.1086/337905","DOIUrl":null,"url":null,"abstract":"Somatic embryogenesis and plantlet regeneration were obtained from mature embryos of red spruce, Picea rubens Sarg. Embryogenic tissues were produced from both 5- and 20-yr-old seed collections. The basal medium used was von Arnold and Eriksson's (AE) salt formulation supplemented with 1,000 mg/L casein hydrolysate, 250 mg/L L-glutamine, 10 μM each of naphthalene acetic acid and N6-benzyladenine (BA), 2% sucrose, and 0.3% Gelrite Gellan gum. Tissues were incubated in the dark at 26 C. Longterm cultures were maintained on the above medium, but with 5 μM BA. Tissues were cultured on phytohormone-free basal medium containing 1% activated charcoal for 7 d, and for maturation were transferred to basal medium containing 20-50 μM abscisic acid. When embryos appeared to be morphologically similar to fully imbibed zygotic embryos, they were removed for germination. They were partially dried and germinated on 1/2 AE at 24 C under reduced light. Plantlets were transferred to sterile peat moistened with 1/4 AE for further growth.","PeriodicalId":9213,"journal":{"name":"Botanical Gazette","volume":"152 1","pages":"446 - 452"},"PeriodicalIF":0.0000,"publicationDate":"1991-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1086/337905","citationCount":"63","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Botanical Gazette","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1086/337905","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 63
Abstract
Somatic embryogenesis and plantlet regeneration were obtained from mature embryos of red spruce, Picea rubens Sarg. Embryogenic tissues were produced from both 5- and 20-yr-old seed collections. The basal medium used was von Arnold and Eriksson's (AE) salt formulation supplemented with 1,000 mg/L casein hydrolysate, 250 mg/L L-glutamine, 10 μM each of naphthalene acetic acid and N6-benzyladenine (BA), 2% sucrose, and 0.3% Gelrite Gellan gum. Tissues were incubated in the dark at 26 C. Longterm cultures were maintained on the above medium, but with 5 μM BA. Tissues were cultured on phytohormone-free basal medium containing 1% activated charcoal for 7 d, and for maturation were transferred to basal medium containing 20-50 μM abscisic acid. When embryos appeared to be morphologically similar to fully imbibed zygotic embryos, they were removed for germination. They were partially dried and germinated on 1/2 AE at 24 C under reduced light. Plantlets were transferred to sterile peat moistened with 1/4 AE for further growth.