GROWTH AND MAINTENANCE OF AN EMBRYOGENIC CELL-CULTURE OF DAYLILY (HEMEROCALLIS) ON HORMONE-FREE MEDIUM

被引:25
|
作者
SMITH, DL [1 ]
KRIKORIAN, AD [1 ]
机构
[1] SUNY STONY BROOK,DEPT BIOCHEM & CELL BIOL,STONY BROOK,NY 11794
基金
美国国家航空航天局;
关键词
HEMEROCALLIS CV AUTUMN BLAZE; DAYLILY; SOMATIC EMBRYOGENESIS; HORMONE-FREE MEDIUM; TISSUE CULTURE;
D O I
10.1093/oxfordjournals.aob.a088180
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Callus cultures of the diploid daylily (Hemerocallis) clone 'Autumn Blaze' were initiated and maintained in hormone-containing nutrient medium. At various times (from 6 weeks to 1 year) after being initiated, hormone-derived cultures were evaluated for their ability to be maintained and to multiply on hormone-free medium at low pH (between pH 4 and 4.5). Cultures had to be exposed to hormone-containing medium for at least 12 weeks before they could be maintained on hormone-free medium at low pH. The transition to maintainability on low pH hormone-free medium included the production of many aberrant embryonal forms ('neomorphs'). However, all hormone-derived cultures tested consisted entirely of preglobular stage proembryos (PGSPs) after 12-24 weeks on low pH hormone-free medium. PGSP cultures have been maintained and multiplied as such for over 1 year on low pH hormone-free medium. PGSPs continue their development into various somatic embryo stages when cultured on hormone-free medium buffered at pH 5.8. The production of well-formed somatic embryos was greatly enhanced when PGSPs were plated on activated charcoal impregnated filter papers that were placed on top of the agar surface. The gross morphology and histology of the PGSPs and stages of somatic embryo development are presented. The work shows that the ability of hormone-free medium at low pH to permit PGSP multiplication without development into later stages of embryo development is not restricted to carrot. © 1991 Annals of Botany Company.
引用
收藏
页码:443 / 449
页数:7
相关论文
共 50 条
  • [31] MAINTENANCE OF SEPARATED RAT PITUITARY MAMMOTROPHS IN CELL-CULTURE
    SNYDER, J
    WILFINGER, W
    HYMER, WC
    ENDOCRINOLOGY, 1976, 98 (01) : 25 - 32
  • [32] MAINTENANCE AND MULTIPLICATION OF BESNOITIA-BESNOITI IN CELL-CULTURE
    GOBEL, E
    VONANGERER, H
    REIMANN, M
    WIDAUER, R
    MUNZ, E
    ZENTRALBLATT FUR BAKTERIOLOGIE MIKROBIOLOGIE UND HYGIENE SERIES A-MEDICAL MICROBIOLOGY INFECTIOUS DISEASES VIROLOGY PARASITOLOGY, 1987, 267 (02): : 286 - 287
  • [33] GROWTH-HORMONE SECRETION BY NORMAL AND TUMOROUS HUMAN PITUITARY SOMATOTROPHS IN CELL-CULTURE
    ADAMS, EF
    JEER, HS
    MASHITER, K
    NEUROENDOCRINOLOGY LETTERS, 1985, 7 (02) : 74 - 74
  • [34] GROWTH-MEDIUM FOR THE EVALUATION OF ANTIESTROGENIC COMPOUNDS IN MCF-7 CELL-CULTURE
    JAIN, PT
    PENTO, JT
    METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY, 1991, 13 (09): : 595 - 598
  • [35] NEW MAINTENANCE MEDIUM FOR CELL CULTURE
    BARON, S
    LOW, RJ
    SCIENCE, 1958, 128 (3315) : 89 - 90
  • [36] CELL-CULTURE ASSAY FOR FOLLICLE-STIMULATING-HORMONE
    BEERS, WH
    STRICKLAND, S
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1978, 253 (11) : 3877 - 3881
  • [37] CHICKEN KIDNEY CELL-CULTURE IN MEDIUM WITHOUT SERUM
    YAMAGUCHI, S
    KAWAMURA, H
    NATIONAL INSTITUTE OF ANIMAL HEALTH QUARTERLY, 1977, 17 (02) : 54 - 57
  • [38] SERUM-FREE MEDIUM OPTIONS FOR CHINESE-HAMSTER OVARY (CHO) CELL-CULTURE
    TILKINS, ML
    JUDD, D
    WEISS, S
    BOIME, I
    PIXLEY, M
    GORFIEN, SF
    MOLECULAR BIOLOGY OF THE CELL, 1992, 3 : A187 - A187
  • [39] STUDIES ON NUTRITION OF RICE CELL-CULTURE .1. SIMPLE, DEFINED MEDIUM FOR RAPID GROWTH IN SUSPENSION CULTURE
    OHIRA, K
    OJIMA, K
    FUJIWARA, A
    PLANT AND CELL PHYSIOLOGY, 1973, 14 (06) : 1113 - 1121
  • [40] GROWTH OF HUMAN ESOPHAGEAL EPITHELIUM IN CELL-CULTURE
    ZBORALSKE, FF
    BRADLEY, BR
    KARASEK, MA
    CLINICAL RESEARCH, 1982, 30 (01): : A93 - A93