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1.
Embryogenic callus cultures were obtained upon repeated sub-culture of non-embryogenic callus from nodal segments of Cymbopogon martinii (Roxb.) Wats. Murashige and Skoog's medium supplemented with 1mg/l 2,4-dichlorophenoxyacetic acid and 0.5 mg/l kinetin and Linsmaier and Skoog's medium supplemented with 2mg/l 2,4-dichlorophenoxyacetic acid and 0.4 mg/l kinetin were used as maintenance media for non-embryogenic and embryogenic cultures, respectively. Plant regeneration occurred through organogenesis in MS basal media containing 2 mg/l kinetin, 1 mg/l 6-benzylaminopurine, 0.2 mg/l biotin, 0.2 mg/l Ca-pantothonate and 0.1 mg/l napthalene acetic acid. Embryogenesis was induced in LS medium supplemented with 1 mg/l kinetin, 0.5 mg/l 6-benzylaminopurine and 0.1 mg/l 3-indole acetic acid. Plant regeneration at high frequency was recorded both through organogenesis and embryogenesis in different passages of long term callus cultures.Abbreviation MS
Murashige and Skoog medium
- LS
Linsmair and Skoog medium
- BAP
6-benzylaminopurine
- kin
kinetin
- 2,4-D
2,4-Dichlorophenoxyacetic acid
- IAA
Indole-3-acetic acid
- CH
Casein hydrolysate
- CaP
calcium pantothonate
- NAA
napthalene acetic acid 相似文献
2.
P. Jha C. B. Yadav V. Anjaiah V. Bhat 《In vitro cellular & developmental biology. Plant》2009,45(2):145-154
An efficient in vitro plant regeneration protocol through somatic embryogenesis and direct shoot organogenesis has been developed for pearl millet
(Pennisetum glaucum). Efficient plant regeneration is a prerequisite for a complete genetic transformation protocol. Shoot tips, immature inflorescences,
and seeds of two genotypes (843B and 7042-DMR) of pearl millet formed callus when cultured on Murashige and Skoog (MS) medium
supplemented with varying levels of 2,4-dichlorophenoxyacetic acid (2,4-D; 4.5, 9, 13.5, and 18 μM). The level of 2,4-D, the
type of explant, and the genotype significantly effected callus induction. Calli from each of the three explant types developed
somatic embryos on MS medium containing 2.22 μM 6-benzyladenine (BA) and either 1.13, 2.25, or 4.5 μM of 2,4-D. Somatic embryos
developed from all three explants and generated shoots on MS medium containing high levels of BA (4.4, 8.8, or 13.2 μM) combined
with 0.56 μM 2,4-D. The calli from the immature inflorescences exhibited the highest percentage of somatic embryogenesis and
shoot regeneration. Moreover, these calli yielded the maximum number of differentiated shoots per callus. An efficient and
direct shoot organogenesis protocol, without a visible, intervening callus stage, was successfully developed from shoot tip
explants of both genotypes of pearl millet. Multiple shoots were induced on MS medium containing either BA or kinetin (4.4,
8.8, 17.6, or 26.4 μM). The number of shoots formed per shoot tip was significantly influenced by the level of cytokinin (BA/kinetin)
and genotype. Maximum rooting was induced in 1/2 strength MS with 0.8% activated charcoal. The regenerated plants were transferred
to soil in pots, where they exhibited normal growth. 相似文献
3.
Li Liu Xiaoli Fan Junwei Zhang Meiling Yan Manzhu Bao 《In vitro cellular & developmental biology. Plant》2009,45(6):673-680
In this study, we have demonstrated that Zoysia japonica callus induced from mature seeds can produce high frequencies of plant regeneration and somatic embryogenesis, even following
a prolonged period of subculturing. Initial callus cultures were induced from mature seeds of Japanese lawngrass (Z. japonica Steud.) incubated on a medium containing major N6 medium salts, minor Murashige and Skoog (MS) medium salts, and modified MS medium organic elements supplemented with 3 mg
L−1 2,4-dichlorophenoxyacetic acid (2,4-D) and 0.01–0.02 mg L−1 6-benzyladenine. Compact callus were selected and subcultured monthly on a medium containing 2 mg L−1 2,4-D, 0.5 mg L−1 kinetin, 500 mg L−1 casein hydrolysate, 500 mg L−1 proline, and 500 mg L−1 myoinositol. Callus maintained in vitro for 18 mo could be induced to regenerate plantlets with a frequency of >90%. By contrast, 36-mo-old callus cultures failed
to produce normal shoot regeneration. However, the addition of CuSO4 to the subculture media maintained >90% regeneration frequencies in such long-term callus cultures. Histological observations
revealed that plant regeneration occurred both through somatic embryogenesis and organogenesis pathways. The ability to sustainable
regeneration in long-term callus cultures will be valuable to the program of genetic transformation and somaclonal variant
selection. 相似文献
4.
Simple hormonal regulation of somatic embryogenesis and/or shoot organogenesis in caryopsis cultures of Pogonatherum paniceum (Poaceae) 总被引:1,自引:1,他引:0
Wenguo Wang Xiaoguang Zhao Guoqing Zhuang Shenghua Wang Fang Chen 《Plant Cell, Tissue and Organ Culture》2008,95(1):57-67
Pogonatherum paniceum (Poaceae) is a perennial plant with good potential for eco-recovery and ornamental function. This study presents in vitro
culture systems of simple hormonal regulation of somatic embryogenesis and shoot organogenesis from mature caryopses. Mature
caryopses of P. paniceum were grown on Murashige and Skoog medium with 3% sucrose (w/v) and various concentrations or combinations of 2,4-dichlorophenoxyacetic
acid (2,4-D), α-naphthaleneacetic acid (NAA) and 6-benzylaminopurine (BAP). Morphological development was analyzed by light
microscope after histological sectioning. Four types of callus were induced by different concentrations of 2,4-D. Type I callus
was regenerated via somatic embryogenesis; type II callus failed to produce any regeneration; type III callus had both somatic
embryogenesis and shoot organogenesis capacities; and type IV callus only displayed shoot organogenesis capacity. Regarding
hormone combinations used in this study, NAA only induced type IV callus and BAP only induced direct multiple shoot formation.
The combinations of 2,4-D and NAA induced type III callus. Several of the regeneration pathways were simply controlled by
one or two kinds of plant hormones. The established systems will be helpful for further research on the developmental mechanism
of switch between somatic embryogenesis and shoot organogenesis. 相似文献
5.
Dominick V. Basile Nasrin Akhtari Yolanda Durand M. S. R. Nair 《In vitro cellular & developmental biology. Plant》1993,29(3):143-147
Summary
Artemisia annua L. is the source of a potent antimalarial, artemisinin. As part of a program to produce artemisinin through tissue culture,
a series of 14 multifactorial experiments were conducted to determine suitable conditions for initiating and maintaining friable
callus fromA. annua. In the first six experiments, three different nutrient formulations [Gamborg B5 (B5), Murashige and Skoog (MS), and Whetmore
and Rier (WR)], each with 32 combinations of auxins and cytokinins [2,4-dichlorophenoxyacetic acid (2,4-D) with benzyladenine
(BA), or 1-naphthaleneacetic acid (NAA) with 6-furfurylaminopurine (kinetin)], were tested. Both B5 and WR nutrients supported
friable callus formation from leaf explants with some combinations of auxin and cytokinin. Inasmuch as friable callus seemed
to be produced over a wider range of auxin and cytokinin concentrations in combination with B5, the remaining experiments
were conducted solely with this nutrient formulation. In the remaining eight experiments, it was determined that friable callus
formed when combinations of NAA with kinetin or 2,4-D and BA were used with B5 medium. Lighter colored, more friable callus
formed in response to 2,4-D and BA than with NAA and kinetin. No single combination of concentrations of auxin and cytokinin
seemed to be “ideal” for producing friable callus. Ranges of 2,4-D from 0.5 to 2.0 with BA between 0.025 and
0.1, or NAA between 0.5 and 2.0 with kinetin between 0.5 and 1.0 mg/liter, produced acceptable results. 相似文献
6.
Margherita Beruto Paolo Curir Pierre Debergh 《In vitro cellular & developmental biology. Plant》1996,32(3):154-160
Summary The effect of cytokinin on growth and plant regeneration of thalamus-derived calluses ofRanunculus asiaticus L. has been investigated with various concentrations of 6-benzyladenine and 6-furfurylaminopurine (kinetin), in a medium
containing 2,4-dichlorophenoxyacetic acid levels, which was decreased to 0 over three subcultures. Cytokinins, although not
essential, for initiating callus production, improved subsequent callus growth and plant regeneration. No somatic embryogenesis
was observed on calluses grown on media lacking cytokinins or containing only kinetin. Calluses manifested embryogenesis on
media containing 6-benzyladenie plus kinetin or only 6-benzyladenine. Nondifferentiating callus was characterized by a high
content of phenolic polymers and an elevated peroxidase and polyphenol oxidase activity in comparison with differentiating
callus. Differences in simple phenol concentrations were observed in the two kinds of callus. 相似文献
7.
Callus was induced in different somatic organs of Oryza sativa L. Specific minimum 2,4-dichlorophenoxyacetic acid (2,4-D) concentrations in the medium were necessary for the induction of callus from different organs while high levels of 2,4-D (6–10 mg/l) induced callus formation in each organ tested. The optimum 2,4-D concentration for callus induction and growth for root-derived calli was 2 mg/l and for leaf-derived 6 mg/l. Root and shoot organogenesis were induced in both root- and leaf-derived calli by sub-culturing to a medium lacking 2,4-D. Root organogenesis occurred at a higher frequency than shoot organogenesis. Shoot organogenesis rarely occurred in calli without differentiated roots. Increased age of callus cultures almost completely inhibited shoot development. The addition of the cytokinin 6-γ,γ-dimethylallyl-amino purine partially restored the potential for shoot organogenesis. Whole plants were easily recovered from the calli and grown to maturity with some plants exhibiting phenotypic abnormalities. 相似文献
8.
Plantlet regeneration through indirect somatic embryogenesis was attempted from rhizome derived callus of Cymbopogon winterianus Jowitt (cv. Jorlab2). Optimum callus was induced on Murashige and Skoog (MS) basal medium supplemented with 4 mg dm−3 2,4-dichlorophenoxyacetic acid (2,4-D). Initially the callus was friable, shiny white and watery in nature. After subculturing
on MS medium containing 2,4-D and kinetin (Kn), callus was transferred onto the MS medium supplemented with 2,4 -D, Kn and
coconut water to induce somatic embryogenesis. Optimum somatic embryogenesis (78.33 %) was achieved on MS medium containing
3.0 mg dm−3 2,4-D and 0.5 mg dm−3 Kn. High frequency (65 %) plantlet conversion from embryos was achieved in MS medium supplemented with 2 mg dm−3 N6-benzyladenine (BA), 0.5 mg dm−3 Kn, 0.2 mg dm−3 calcium pantothenate and 0.2 mg dm−3 biotin. 相似文献
9.
R. V. Sairam C. Wilber J. Franklin B. Smith J. Bazil R. Hassel D. Whaling K. Frutiger C. A. Blakey R. Vierling S. L. Goldman 《In vitro cellular & developmental biology. Plant》2002,38(5):435-440
Summary A protocol for high-frequency callus, somatic embryogenesis, and plant regeneration for Tripsacum is described. Plants were regenerated from complete shoot meristems (3–4 mm) via organogenesis and embryogenesis. In organogenesis,
the shoot meristems were cultured directly on a high cytokinin medium comprising 5–10 mgl−1 (22.2–44.4 μM) 6-benzyladenine (BA). The number of multiple shoots varied from six to eight from each meristem. The time required for production
of plants from organogenesis was rapid (4–6 wk). In contrast, callus was induced on an auxin medium and continuously cultured
on an auxin medium for production of somatic embryos. Prolific callus with numerous somatic embryos developed within 3–4 wk
when cultured on an auxin medium containing 5 mgl−1 (22.6μM), 2,4-dichlorophenoxyacetic acid (2,4-D). The number of shoots induced varied from two to five per callus. Regardless of
the cultivars used, the frequency of callus induction and plant regeneration was between 48% and 94%. The seed germination
procedures also were modified and resulted in a maximum of 60–80% seed germination. Finally, the rate of T-DNA transfer to
complete shoot meristems of Tripsacum was high on the auxin medium and was independent of whether super-virulent strains of Agrobacterium were used or not. 相似文献
10.
Keith A. Walker Poli C. Yu Shirley J. Sato E. G. Jaworski 《American journal of botany》1978,65(6):654-659
Organogenesis in alfalfa callus (Medicago sativa L. cv. ‘Regen S’) has been obtained by the transfer of callus from an induction medium containing growth regulators to a regeneration medium lacking growth regulators. The transfer of callus from induction medium containing high levels of 2,4-D and low levels of kinetin to regeneration medium resulted in the formation of shoots. Conversely, the transfer of callus from induction medium containing low levels of 2,4-D and high levels of kinetin resulted in the formation of roots. The pattern of organogenesis on regeneration medium was modified by the nutritional composition of that medium. When Blaydes medium supplemented with inositol and yeast extract was employed as regeneration medium, root organogenesis was inhibited. Root organogenesis was not inhibited by either Shenk and Hildebrandt medium or Gamborg's B5 medium. Shoot formation occurred on all of these media. A survey of the in vitro organ-forming capacity of 14 genotypic clones from the cv. ‘Regen S’ was conducted. The capacity to form organs differed quantitatively among the clones analyzed. A more detailed analysis of a highly responsive clone (RA3) and a poorly responsive clone (RA5) revealed no significant qualitative difference in their organogenic responses. 相似文献
11.
Immature inflorescences of kodo millet (Paspalum scrobiculatum L. cv. GPUK-3) were cultured on MS medium. Induction of embryogenic callus and subsequent somatic embryogenesis was possible
on both 2,4-D and Picloram alone or with kinetin from spikelets as well as rachis. Immature inflorescence cultured on medium
supplemented with lower levels of Picloram in combination with kinetin developed organogenic callus with shoot buds. Direct
somatic embryo formation on rachis was observed at higher levels of Picloram in combination with kinetin. Plant regeneration
was observed when calluses were transferred to α-napthaleneacetic acid (NAA) plus 6-benzylaminopurine (BA) supplemented MS
medium. Histological observations provided a clear evidence for both somatic embryogenesis and shoot organogenesis. Profuse
rooting was induced on phenylacetic acid (PAA) supplemented medium. Regenerated plants were successfully transferred to pots
under field conditions where most of the plants survived and set normal seeds. 相似文献
12.
Effects of cytokinin on adventitious root formation in callus cultures ofVigna unguiculata (L.) walp
Woong-Young Soh Pil-Son Choi Duck-Yee Cho 《In vitro cellular & developmental biology. Plant》1998,34(3):189-195
Summary Yellowish compact callus, induced from cowpea hypocotyls on Murashige and Skoog(MS) medium (1962) containing 0.2 mg/l(0.93
μM) kinetin and 0.4 mg/l (1.81 μM) 2,4-dichlorophenoxyacetic acid (2,4-D), was subcultured on MS medium containing cytokinin alone, auxin alone, or auxins
plus cytokinins in order to determine the effect of cytokinins on root organogenesis in callus cultures. The callus actively
proliferated on the same medium but did not show any organogenic activity macroscopically as well as microscopically. On medium
with N6-benzyladenine (BA) and 1-naphthaleneacetic acid (NAA), the yellowish compact callus first changed to pale green compact callus
and then many green spots appeared on its surface under light culture. But the yellowsih compact callus remained yellowish
and white spots appeared on its surface in dark culture. These spots gradually became white nodular structures. Adventitious
root formation from the nodular structures occurred not only on the same medium, but also on medium with either auxin or cytokinin
but not both. Yellowish compact callus on medium with auxin alone was transformed to yellowish friable callus, which did not
develop adventitious roots. The yellowish friable callus could gain rhizogenic activity only after morphological modification
to pale green compact callus on medium with auxin plus cytokinin. The modified callus did not form adventitious roots on medium
with auxins but only with cytokinins. Therefore, it is suggested that cytokinins have stimulating effects on root formation
from callus that previously did not show rhizogenic activity on medium with auxins alone. In addition, the rhizogenic potential
of cowpea callus was discriminated from that of leaf explants, which formed adventitious roots directly on medium with auxin
alone. 相似文献
13.
Margarita Cacho Margarita Morán María Teresa Herrera Jorge Fernández-Tárrago 《Plant Cell, Tissue and Organ Culture》1991,25(2):117-123
The effects of the auxins 2,4-D, NAA and IAA either alone or in combination with kinetin or BA were investigated to assess the morphogenetic potential of leaf, root and hypocotyl explants of Digitalis thapsi. Calluses were obtained from the three explants in basal medium without the addition of growth regulators and in leaves, the calluses formed roots. Application of 2,4-D, NAA or BA increased callus formation. The presence of NAA induced root formation and that of BA induced shoot formation via callus interphase. Indole-3-acetic acid alone only induced the generation of roots in the hypocotyl callus. Kinetin was ineffective in all the explants tested. Combinations of NAA with kinetin or BA were more effective in inducing organogenesis in leaf explants. Optimum responses were obtained in hypocotyl and root explants by using IAA in combination with BA, the highest rate of shoot regeneration being observed in hypocotyl explants.Rooting of the differentiated shoots was readily achieved in media without growth regulators. Regenerated plantlets were transferred to soil and grew with a survival rate of 70%.Abbreviations BA
benzyladenine
- 2,4-D
2,4-dichlorophenoxyacetic acid
- IAA
indoleacetic acid, Kin-kinetin
- NAA
naphthaleneacetic acid 相似文献
14.
《Plant science》1987,51(1):93-96
Somatic embryogenesis and subsequent formation of plantlets was achieved from callus cultures derived from mature zygotic embryos of Sinocalamus latiflora (Munro) McClure (Bamboo). Embryogenic callus was initiated on Murashige and Skoog's medium (MS) supplemented with 6 mg/l 2,4-dichlorophenoxyacetic acid (2,4-D), 3 mg/l kinetin, 250 mg/l polyvinylpyrrolidon and 5% sucrose. Prolonged culture of the embryogenic callus on the same medium resulted in embryoid formation. The embryoids developed further to yield whole plantlets when transferred to a medium containing lower concentrations of 2,4-D (3 mg/l) and kinetin (2 mg/l). 相似文献
15.
在以幼穗为外植体的诱导培养及其以后的继代培养与悬浮培养中,从以下几个方面对3个籼稻品种的体细胞胚胎发生(E)与器官发生(O)的特点作了比较研究.在形态上,(E)型愈伤由胚状体组成,具有层次分明的结构.胚状体由胚芽、胚根及盾片组成.而(O)型的愈伤没有上述组织的分化.没有层次结构。植株再生能力方面.与器官发生途径相比较,体细胞胚胎发生途径之分化频率高.保持再生能力持续的时间长.从每个愈伤上发生的再生植株数多.(O)型愈伤结构较疏松.建立结构良好的、细胞团较小的悬浮细胞系容易.但这种细胞系在液体条件下几乎丧失再生能力.而(E)型愈伤则相反.建立好的悬浮细胞系.需要时间较长.但在悬浮条件下仍然具有再生植株的能力。在诱导条件方面.2,4-D及激动素分别作用时可诱导器官发生,共同作用时则诱导体细胞胚胎发生.再生植株途径方面,由于水稻同时具有器官发生及体细胞胚胎发生的特点.无论在诱导条件上还是在(E)与(O)本身的特点上均不似萝卜或烟草那样专一.并且有(E)与(O)相互转化和混合发生的复杂情况. 相似文献
16.
Excised stem explants of Antirrhinum majus L. var. Kymosyblanc were grown in a denned medium to investigate factorsinfluencing bud and root development, callus induction, andsomatic embryogenesis. Auxins such as indoleacetic acid (IAA)and naphthaleneacetie acid (NAA) caused limited callus developmentand abundant root formation, whereas 2,4-dichlorophenoxyaceticacid (2,4-D) promoted soft friable callus with embryos and occasionaldevelopment of thick abnormal roots. 2-Naphthoxyacetic acid(NOA) and coconut milk (CM) used together induced friable greencallus growth and differentiation of small globular embryoswhich eventually developed into plantlets after transfer toauxin-free agar mineral medium containing sucrose. Cytokininssuch as benzyladenine (BA), zeatin, and kinetin induced compactgreen callus but in the absence of auxin failed to promote organogenesis.The interaction of IAA and kinetin resulted in the regenerationof the whole plant from stem explants. When NAA was used withkinetin, shoot development was totally inhibited and abundantroots were formed. Thus, the alternative morphogenetic eventsprobably reflect the biochemical subtleties occurring withinthe callus as a result of differences of actual endogenous levelsof growth substances in the tissues studied. These experimentshave been performed and interpreted on a histological basis. 相似文献
17.
Ning Zhang Wei Fang Yan Shi Qianqian Liu Haiyun Yang Renyi Gui Xinchun Lin 《Plant Cell, Tissue and Organ Culture》2010,103(3):325-332
In this study, mature zygotic embryos, plant growth regulators, and various media were tested with the aim of developing an efficient regeneration system for plantlets of the bamboo species Dendrocalamus hamiltonii. Callus formation was induced in explants cultured in Murashige and Skoog (MS) medium supplemented with 1.0–3.0 mg/l 2,4-dichlorophenoxyacetic acid. Optimal shoot differentiation and subsequent shoot growth were also obtained in MS medium supplemented with 2 mg/l benzyladenine, 1 mg/l kinetin, and 1 mg/l naphthaleneacetic acid. Root induction was enhanced by the addition of 5 mg/l indole-3-butyric acid to the culture medium. Histological analysis revealed that both somatic embryogenesis and organogenesis were induced during callus initiation, shoot differentiation, and the development of plantlets from the mature zygotic embryos. Our data provide a useful basis for developing culture protocols for the regeneration of bamboo plants. 相似文献
18.
Yasunari Ogihara 《Journal of plant research》1979,92(3):163-171
Effects of three different auxins and kinetin in various combinations on greening and redifferentiation of the callus ofHaworthia setata were investigated. All auxins at the concentration of 50 mg/l inhibited callus greening. NAA in combination with kinetin promoted both callus greening and production of redifferentiated
shoots. Low concentrations of IAA without kinetin promoted redifferentiation of shoots, but not callus greening. Addition
of 2,4-D completely inhibited both greening and redifferentiation regardless of the level of kinetin except for the effects
on shoot formation in the medium with 0.1 mg/l 2,4-D added. The calluses with the highest chlorophyll content were observed in the medium containing 2.0 mg/l kinetin without any auxins or with 0.1 mg/l NAA added. Most frequent shoot redifferentiation was observed in the medium containing 0.1 mg/l IAA without kinetin (redifferentiation rate; 67%), followed by the medium containing 10 mg/l NAA with 2.0 mg/l kinetin (44%), and 0.1 mg/l 2,4-D with 0.2 mg/l kinetin (33%). Generally, higher degrees of greening were associated with better growth. However, the auxins (IAA, NAA and
2,4-D) given at concentrations optimal for growth did not exhibit the highest degree of callus greening. Differences of the
three auxins in their actions and interaction with kinetin were disclosed.
Contribution from the Laboratory of Genetics, Faculty of Agriculture, Kyoto University, Japan, No. 423 相似文献
19.
C. A. Martínez A. M. Giulietti J. Rodríguez Talou 《Plant Cell, Tissue and Organ Culture》2011,104(1):91-100
Hypericum perforatum L. (St. John’s wort) produces a number of phytochemicals having medicinal, anti-microbial, anti-viral and anti-oxidative
properties. Plant extracts are generally used for treatment of mild to medium cases of depression. Plant regeneration can
be achieved in this species by in vitro culture of a variety of explants. However, there are no reports of regeneration from
petal explants. In this report plant regeneration from petal explants of St. John’s wort was evaluated. Petals of various
ages were cultured on agarized Murashige and Skoog 1962 (MS) medium supplemented with auxin and cytokinin (kinetin), maintained in the dark and callus and shoot regeneration determined
after 28 days. At an auxin to cytokinin ratio of 10:1, callus and shoot formation were induced by all levels of indole-3-acetic
acid (IAA), indole-3-butyric acid (IBA) and 1-naphthaleneacetic acid (NAA), while 2,4-dichlorophenoxyacetic acid (2,4-D) induced
only callus formation. The optimum level of auxin for shoot regeneration was 1.0 and 0.1 mg/l kinetin, where the regeneration
frequency was 100 percent for all three auxins. The highest number of shoots per explant (57.4 and 53.4) was obtained with
IAA and IBA, respectively. In the absence of auxin, kinetin levels of 0.1 and 0.25 mg/l induce callus and shoot formation
at low frequency but not at lower levels. Callus and shoot formation did not occur in the absence of growth regulators. Petal-derived
shoots were successfully rooted on half-strength MS medium without a requirement for exogenous auxin and flowering plants
were established under greenhouse conditions. From these results it can be concluded that auxin type is a critical factor
for plant regeneration from petal explants of Hypericum perforatum and there is no absolute requirement for high levels of cytokinin. 相似文献
20.
Summary Anthers of Feijoa sellowiana Berg. (feijoa) produced pollen callus when cultured in Murashige and Skoog medium containing 2,4-dichlorophenoxyacetic acid and benzyladenine or in nurse cultures. Somatic callus was also formed in large amounts from the connective and from the cut end of the filament. Anthers containing microspores at the stage immediately prior to the first pollen mitosis cultured in the presence of 3% sucrose, presented the highest frequencies of induction. Androgenetic divisions were initiated by the formation of two morphologically equal cells, the so-called B-pathway. Attempts to regenerate pollen plants were unsuccessful but leaf-like structures could be obtained in regeneration media containing combinations of gibberellic acid and benzyladenine.Abbreviations 2,4-D
2,4-diclorophenoxyacetic acid
- BA
benzyladenine
- FDA
fluorescein diacetate
- GA3
gibberellic acid
- Kn
kinetin
- MS
Murashige and Skoog (1962) medium 相似文献