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1.
Agave arizonica Gentry & Weber, an extremely rare and endangered species native to Arizona, was successfully propagated in vitro using modified
Murashige and Skoog media. Adventitious shoots developed from callus which formed on bulbil explants grown in a medium supplemented
with 1.4 μM 2,4-dichlorophenoxyacetic acid. These shoots proliferated by subculture in media supplemented with 44.4 μM 6-benzylaminopurine,
and either 0.5 or 5.4 μM naphthaleneacetic acid. Rooting occurred on shoots transferred to a growth regulator free medium.
Rooted plants transferred to potting soil could be established under greenhouse conditions following gradual acclimatization
indoors. 相似文献
2.
Mukhopadhyay Madhumita J. Mukhopadhyay Sandip Sen Sumitra 《Plant Cell, Tissue and Organ Culture》2002,69(1):101-104
The present study involves in vitro propagation of Iphigenia indica (Kunth.) through multiplication of whole corms and corm buds. The whole corms produced very small micro-corms, which developed plants individually whereas corm buds multiplied to produce numerous shoots at variable rates in presence of -naphthaleneacetic acid (NAA) and 6-benzylaminopurine (BAP). The best response in corm and bud multiplication was obtained in Murashige and Skoog's basal medium (MS) supplemented with 2.69 M NAA and 8.88 M BAP. The shoots regenerated were further cultured on MS medium containing NAA and indole-3-butyric acid (IBA) for initiation of roots. MS medium with 5.38 M NAA and 4.92 M IBA induced highest percentage of roots (81%) within 2 weeks in culture. 相似文献
3.
The initiation and development of somatic embryos and organogenic shoots and corm-like structures (CLSs) from petiole-derived
calli of Amorphophallus rivieri Durieu were observed histologically. The petioles were cultured on Murashige and Skoog (MS) medium supplemented with 5.37 μM
α-naphthaleneacetic acid (NAA) and 4.44 μM N6-benzylaminopurine (6-BA) for callus induction. The shoot and corm organogenesis occurred from the compact calli when they
were transferred to a medium containing 0.54 μM NAA and 4.44 μM 6-BA. A combination of 13.57 μM 2,4-dichlorophenoxyacetic
acid (2,4-D) and 8.88 μM 6-BA or 24.18 μM NAA and 6.66 μM 6-BA was optimum for induction of somatic embryos, which failed
to produce plantlets because of their structural abnormalities. Shoot regeneration predominantly happened through organogenesis
although somatic embryogenesis infrequently occurred. The subepidermal cells of the compact callus converted to competent
cells and started divisions, which resulted in formation of the meristemoids. The meristemoid cells continued division to
develop into bud primordia. Subepidermal cells could also form the globular structures. Subsequently, these globoids developed
into CLSs from which plantlets regenerated during subculture. Meanwhile, the CLSs were capable to form cormels, which could
be a promising way for the propagation of A. rivieri. 相似文献
4.
Crown and leaf slices of in vitro plantlets of a non-flowering Vetiveria zizanioides from Java were used to induce compact calli and to regenerate plantlets. The influence of different growth regulators (2,4-dichlorophenoxy
acetic acid, 6-benzylaminopurine), sucrose concentrations (10–100 g l−1), cultivation in light or dark, and cultivation time on callus induction medium (6 or 12 weeks), on the induction of compact
callus and the subsequent regeneration of plantlets was studied. Up to 75% of crown slices cultured on modified Murashige
and Skoog medium supplemented with 2.26 μM 2,4-dichlorophenoxy acetic acid, 2.22 μM 6-benzylaminopurine and 75 g l−1 sucrose developed compact callus. For subsequent regeneration of plantlets, callus induction in the light for 6 weeks on
the callus induction medium containing 10 g l−1sucrose, and subsequent transfer to the regeneration medium, was the best procedure, regenerating plantlets on around 60%
of the crown or leaf slices, with up to 100 plantlets per slice. We have compared the efficiency of the above mentioned procedure
with several other methods to regenerate plantlets. Our findings indicate that the procedure developed in this study was best
in regenerating plantlets for the used vetiver variant.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
5.
Summary A method for adventitious shoot induction from petiole explants of Heracleum candicans is reported. Shoot buds were induced on Murashige and Skoog (MS) medium with 4.4μM 6-benzylaminopurine (BA) and 1.1 μM 2,4-dichlorophen-oxyacetic acid (2,4-D). A wound response in the presence of BA and 2,4-D at the time of culture was necessary
for inducing shoot buds. The shoot bud regeneration was significantly influenced by size, type and orientation of explants
on the culture medium. These shoot buds developed into 4–5 cm shoots upon transfer to a medium containing 1.1μM BA and 0.5 μM α-naphthaleneacetic acid (NAA). The regenerated shoots formed rooted plantlets on MS medium supplemented with 4.9 μM indole-3-butyric acid (IBA). About 15 plants were established in the field for further evaluation. 相似文献
6.
Vengadesan G. Ganapathi A. Prem Anand R. Ramesh Anbazhagan V. 《Plant Cell, Tissue and Organ Culture》2000,61(1):23-28
In vitro morphogenesis via organogenesis was achieved from callus cultures derived from hypocotyl explants of Acacia sinuata on MS (Murashige and Skoog, 1962) medium. Calli were induced from hypocotyl explants excised from 7-day-old seedlings on
MS medium containing 3% sucrose, 0.8% agar, 6.78 μM 2,4-dichlorophenoxyacetic acid and 2.22 μM 6-benzylaminopurine. Regeneration
of adventitious buds from callus was achieved when they were cultured on MS medium supplemented with 10% coconut water, 13.2
μM 6-benzylaminopurine and 3.42 μM indoleacetic acid. Addition of gibberellic acid (1.73 μM) favored shoot elongation. Regenerated
shoots produced prominent roots when transferred to half strength MS medium supplemented with 7.36 μM indolebutyric acid.
Rooted plantlets, thus developed were hardened and successfully established in the soil. This protocol yielded an average
of 20 plants per hypocotyl explant over a period of 4 months.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
7.
Landi Sun Suiwen Hou Dali Wu Yingcong Zhang 《In vitro cellular & developmental biology. Plant》2008,44(5):396-400
This study describes a reliable protocol for callus induction and rapid mass propagation of the ecologically important plant,
Zygophyllum xanthoxylon (Bunge) Maxim. The optimum callus induction medium was Murashige and Skoog (MS) supplemented with 4.4 μM 6-benzylaminopurine
(BAP) and 2.7 μM α-naphthalene–acetic acid (NAA), on which the callus induction frequencies from different seedling explants
were all 100%. However, seedling-derived callus did not form regenerated shoots. In order to achieve shoot multiplication,
shoots were developed from cultured plumules, at an average of 3.1 shoots per explant, and the regenerated shoot tips were
further multiplied by subculture. The best shoot multiplication from shoot tips was achieved on MS supplemented with 5.4 μM
NAA and 22.2 μM BAP after 40 d of culture. Seventy-three percent of regenerated shoots formed roots when cultured on MS supplemented
with 8.6 μM IAA after 4 wk of culture. The plants that acclimatized successfully in sand flourished the following year, with
normal morphology and growth characteristics. 相似文献
8.
A procedure is outlined for the establishment of a proliferating cell suspension culture and subsequent plant regeneration
of the latex-producing plant,Calotropis gigantea (Linn.) R. Br. Friable calluses were obtained by culturing hypocotyl explants on modified Murashige and Skoog medium with
2.69 μM α-naphthaleneacetic acid and 4.44 μM 6-benzyl-aminopurine. Friable calluses were transferred to modified Murashige
and Skoog liquid medium containing 500 mg l−1 casein hydrolysate, 5% (v/v) coconut water and 5% (w/v) sucrose to initiate suspension cultures. Suspensions were subcultured
every 10–12 days and supplemented with 13.56 μM 2,4-dichlorophenoxyacetic acid (2,4-D). After 3–4 subcultures, suspensions
consisted of small, highly cytoplasmic cell clumps and large vacuolate cells. Plating the suspension clumps on medium containing
4.52 μM 2,4-dichlorophenoxyacetic acid and culturing in darkness produced macroscopic calluses, which subsequently produced
a high number of shoots when placed in light and supplemented with 2.22 μM 6-benzyl-aminopurine and 0.45 μM 2,4-dichlorophenoxyacetic
acid. Shoots were rooted using Bonner's solution containing 0.49 μM indole-3-butyric acid, and the plants successfully transferred
to soil.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
9.
Inflorescence apices are suitable explants for the rapid in vitro propagation of Musa spp. However, the diploid and triploid banana cultivars showed different in vitro responses with respect to the hormone combinations
in Murashige and Skoog medium. The diploid cultivar (Sannachenkadali, AA) induced a maximum number of multiple shoots in 8.9 μM
6-benzyl adenine (BA) whereas the triploid cultivar (Red banana, AAA) exhibited maximum multiplication in 22.2 μM 6-benzyl
adenine. MS medium supplemented with 11.4 μM indole acetic acid and 17.8 μM BA was also suitable for shoot proliferation in
triploid cultivar but not in the diploid cultivar. The regenerated shoots were rooted in Murashige and Skoog basal medium
within 10–15 days. The rooted plantlets were transferred to vermiculite and maintained at a temperature of 25 ± 2°C for 10 days
and then at room temperature (30–32°C) for 2 weeks before transferring to potted soil compost mixture. The plantlets showed
100% survival. 相似文献
10.
A protocol was developed for the induction, maturation and germination of somatic embryos from leaf tissue of jojoba [Simmondsia chinensis (Link) Schneider]. Explants were placed on their adaxial sides in Petri dishes and maintained in darkness on half-strength
Murashige and Skoog basal medium (MS/2). Combinations of 2,4-dichlorophenoxyacetic acid (1.35–4.52 μM) with 6-benzylaminopurine
(1.33–4.43μM) and 2 synthetic cytokinins, N-(2-chloro-4pyridyl)-N′-phenylurea (1.21–4.03μM) or (E)-6-[3-(trifluoromethyl)-but-2-enylamino]
purine (1.11–3.71μM) resulted in formation of embryogenic cultures and somatic embryos. After two 30-day subcultures, embryogenic
cultures were transferred onto MS/2 medium supplemented with different auxins and cytokinins. Somatic embryo maturation, germination
and plantlet formation were achieved using 1-naphthaleneacetic acid (3.75μM) or indole-3-butyric acid (3.44μM) in combination
with BA (0.44 or 1.33μM) or F3iP (0.37 or 1.11μM). Histology confirmed each stage of development.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
11.
Xiaojiao Han Hongqiang Yang Kaixuan Duan Xinrong Zhang Haizhou Zhao Shuzhen You Qianqian Jiang 《Plant Cell, Tissue and Organ Culture》2009,96(1):29-34
The effects of sodium nitroprusside (SNP) on the multiplication, regeneration and rooting of Malus
hupehensis Rehd. var. pinyiensis Jiang in tissue culture have been investigated. The results showed that the multiplication of plantlets was promoted significantly
by applying 20 μM SNP to the Murashige and Skoog (MS) medium containing 2.0 μM 6-benzylaminopurine (BA) and 1.0 μM zeatin
(ZT). Multiplication of plantlets from the 1st subculture was more sensitive to SNP than that from the 4th or 7th subculture.
The differentiation and regeneration of adventitious shoots from leaves or cotyledons increased significantly when 20–30 μM
SNP was supplied to the medium MS containing 25 μM BA, 2.5 μM α-naphthaleneacetic acid (NAA) and 2.5 μM ZT. Adventitious shoots regeneration frequency from cotyledons was higher than that
from leaves at the presence of SNP. The rooting of plantlets was promoted by SNP significantly and the best result for rooting
was achieved in the half-strength MS medium containing 75 μM SNP. In addition, adventitious roots without callus distributed
at the base of shoots when SNP was supplied. 相似文献
12.
María del Socorro Santos Díaz Candy Carranza Álvarez 《In vitro cellular & developmental biology. Plant》2009,45(2):162-170
Two procedures for the in vitro propagation of Encyclia mariae, a threatened Mexican orchid, were developed. In the first procedure, leaves from in vitro germinated seedlings were cultured on Murashige and Skoog medium (MS) supplemented with the range of 2.21–4.4 μM 6-benzylaminopurine
(BA) in combination with 2.69–10.74 μM naphthalene acetic (NAA), 2.07–8.29 μM indole-3-butyric (IBA), or 2.85–11.42 μM indole-3-acetic
acid (IAA) to determine the best medium for the induction of shooting. Maximum direct shoot formation from leaves was observed
on MS containing 22.21 μM BA and 10.74 μM NAA (25 shoots/explant). The second procedure began with the culture of protocorms
on media containing NAA, IBA, or IAA, which induced callus formation with high regenerative potential in the form of protocorm-like-bodies
(PLBs) that eventually differentiated into shoots. The optimal response was attained when these structures were cultured on
medium with 4.14 μM IBA (30 shoots/PLB). To promote the elongation of shoots derived from PLBs, the material was subcultured
onto MS medium containing 22.21 μM BA and 5.37 μM NAA. Through the exploration of the effects of auxins and matrix on the
rooting of shoots, it was determined that the optimal rooting occurred on media supplemented either with 5.71 μM IAA or 4.14 μM
IBA either on agar-gelled medium or in liquid media with coir as the matrix. Rooting was found to be 20% higher in liquid
media than in agar-gelled medium. 相似文献
13.
Thidiazuron Induced Multiple Shoot Induction and Plant Regeneration from Cotyledonary Explants of Mulberry 总被引:4,自引:0,他引:4
T. Dennis Thomas 《Biologia Plantarum》2003,46(4):529-533
A rapid micropropagation protocol through induced multiple shoots from the cotyledonary explant of mulberry (Morus alba L) is described. The highest number of shoots (20.3) was obtained when explants from 14-d-old embryos were cultured on Murashige
and Skoog (MS) medium supplemented with 7 μM thidiazuron for 45 d. Of the three cultivars used, cv. S-36 was the best followed
by cv. K-2 and S-1. The shoots were transferred to MS medium supplemented with 5 μM 6-benzylaminopurine for elongation. The
elongated shoots were rooted on half strength MS medium containing 1 – 7 μM indole 3-butyric acid or 1-naphthalene acetic
acid. The rooted plants were transplanted to soil with 90 % success. The emerged shoot primordia probably initiated from the
pre-existing meristems since the shoot bud show definite vascular connection to the major vascular tissue.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
14.
Picrorhiza kurrooa Royle ex Benth., a high value medicinal herb of alpine Himalaya and a source of hepatoprotective picrosides, is listed as
‘endangered’ due to heavy collection from its natural habitat. The present report deals with successful propagation of this
species using both conventional and in vitro techniques. Vegetative propagation was achieved by rooting runner cuttings with indole-3-butyric acid (IBA) or α-naphtheleneacetic
acid (NAA) treatment before planting. Nearly 87% rooting success was achieved by treatment of cuttings with 50.0 μM IBA. Seeds were given a presoaking treatment with gibberellic acid (GA3), 6-benzylaminopurine (BAP) or a combination of both to influence germination. More than 11-fold improvement in germination
was recorded in seeds treated with 250.0 μM GA3. In vitro shoot multiplication was achieved through sprouting of axillary buds using nodal segment. Multiple shoots were formed following
culture for 3 weeks on Murashige and Skoog (MS; 1962. Physiologia Plantarum 15: 473–497) medium containing 1.0 μM BAP. Cent
percent rooting success, without basal callus formation, was observed when individual microshoots were placed in MS medium
supplemented with IBA. The plantlets raised using conventional as well as tissue culture methods were hardened and successfully
established in the experimental field located at 2450 m elevation. In addition, strategies have been discussed to encourage
cultivation and in situ conservation of this highly valued medicinal herb so as to reduce pressure on its natural populations. 相似文献
15.
Summary An efficient protocol was established for in vitro shoot multiplication from nodal explants of Clitoria ternatea on semisolid Murashige and Skoog (MS) basal medium supplemented with 8.9μM 6-benzylaminopurine (BA). Inclusion of 1-naphthaleneacetic acid (NAA) in the culture medium along with BA promoted higher
rates of shoot multiplication than BA alone. The rate of shoot multiplication was maximum (5.21) after 4 wk of culture on
MS basal medium supplemented with 8.9μM BA and 1.34μM NAA. The elongated shoots rooted within 7–8d in half-strength MS basal salts supplemented with 1.34μM NAA and 2% (w/v) sucrose. About 85% of the rooted plantlets were acclimatized and transferred to the greenhouse. 相似文献
16.
The ability of the summer flowering Gladiolus dalenii Van Geel and the winter flowering G. tristis L. to form corms in vitro was investigated. G. dalenii spontaneously formed corms on a shoot induction medium consisting of the basal medium of Murashige & Skoog (1962) with up to 2.0 mg l-1 benzyladenine (BA), 3% sucrose and solidified with 2 g l-1 Gelrite®. The effect of different BA and sucrose concentrations as well as different temperatures on in vitro corm production of G. tristis was further investigated. The best production of shoots per explant was achieved on a medium containing 0.5 to 1.0 mg l-1 BA, sucrose concentrations of 6 to 9% and cultured at 15°C. The best corm production was achieved at the same temperature and with the same medium with the exception that BA was omitted from the medium. To test the effect of the osmotic potential on the formation of shoots and corms, sucrose was substituted by mannitol at various concentrations. Sucrose proved to be essential for both shoot and corm production and the use of mannitol had no beneficial effect. 相似文献
17.
A reliable method of plant regeneration has been achieved from decapitated mature embryo axes (DCMEA) explants. Shoots appear
directly from explants of genotype T-15-15 when cultured on Maheswaran and Williams (EC6) basal medium supplemented with N6-benzylaminopurine (BAP) and indole-3-acetic acid (IAA) at various combinations. The shoots elongated on half strength Murashige
and Skoog (MS) medium fortified with 3 μM gibberellic acid. Elongated shoots were rooted with 80 – 85 % efficiency on half
strength MS medium with 0.5 μM indole-3-butyric acid. Survival of plants in the pots was 75 – 80 %. This protocol was used
in Agrobacterium mediated transformation. The DCMEA explants were treated independently with two A. tumefaciens (LBA 4404) strains harbouring a binary vector carrying the green fluorescent protein (GFP) and β-glucuronidase (GUS) reporter
genes, respectively. Both the strains contained neomycin phosphotransferase selectable marker gene. After co-cultivation,
the explants were cultured on EC6 basal medium supplemented with 5 μM BAP and 1 μM IAA. The selection of putative transformants was on a medium containing
50 mg dm−3 kanamycin. Expression of GUS and GFP gene was confirmed by histochemical assay and fluorescence microscopy, respectively.
The elongated shoots expressing GFP reporter gene were rooted and transferred to pots for hardening. The integration of GFP
gene into the genome of putative transformants was confirmed by Southern blotting.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
18.
U. A. Jo H. N. Murthy E. J. Hahn K. Y. Paek 《In vitro cellular & developmental biology. Plant》2008,44(1):26-32
An efficient, simple micropropagation method was developed for Alocasia amazonica using corms in semisolid and liquid cultures. Explants were cultured onto Murashige and Skoog (MS) medium (Murashige and
Skoog, Physiol. Plant. 15:473–497, 1962) supplemented with different cytokinins (Benzyladenine [BA, 2.22–13.32 μM], kinetin [2.32–13.95 μM], Thidiazuron [TDZ, 0.45–4.54 μM])
and cytokinin in combination with auxins [naphthalene acetic acid (NAA, 0.54–5.37 μM)/indole acetic acid (IAA, 0.57–5.71 μM)/indole
butyric acid (IBA, 0.49–4.9 μM)]. All supplementary-induced shoot proliferation and the optimal results was on the medium
supplemented with 2.27 μM TDZ, which induced 5.1 shoots per explant. Among the different concentrations of sucrose (0–120 g
l−1) tested for shoot proliferation, 30 g l−1 was found suitable for corm cultures of Alocasia amazonica. The optimal shoot proliferation and biomass values were with the plantlets grown at 30 μmol m−2 s−1 photosynthetic photon flux (PPF) and 25°C. Liquid cultures found suitable for shoot proliferation and biomass accumulation
was compared to semisolid cultures. Comparative studies of bioreactor systems [continuous immersion (with or without net)
and temporary immersion in liquid media using ebb and flood] revealed that shoot multiplication and growth were greatest with
the raft bioreactor system. Plantlets (cormlets) from the bioreactor were hydroponically cultured for 30 days, and 100% of
plants were acclimatized successfully. The simple efficient method of production of plantlets (cormlets) is useful for large-scale
multiplication of this important ornamental plant.
An erratum to this article can be found at 相似文献
19.
Callus cultures from zygotic embryos of neem (Azadirachta indica) were initiated and analyzed for azadirachtin production. Medium components were screened and optimized using the statistical
techniques of Plackett–Burman and response surface methodology. The Plackett–Burman design, with five medium components (Murashige
and Skoog major salts, sucrose, casein hydrolysate, indole-3-acetic acid, and N6-benzylaminopurine), was performed to screen the variables that significantly affected azadirachtin production. The three
variables—Murashige and Skoog major salts, sucrose, and N6-benzylaminopurine—significantly affected azadirachtin production and were significant factors for optimization using response
surface methodology. The experimental results were fitted to a second-order polynomial model with a correlation coefficient
(R
2) of 0.9582. The optimal concentrations of variables for maximum azadirachtin production were full-strength Murashige and
Skoog major salts, 5.68% sucrose, and 10.42 μM N6-benzylaminopurine. The maximum azadirachtin production by the predicted model was 5.13 mg/g dry weight, which was in agreement
with the actual experimental value of 4.97 mg/g dry weight. 相似文献
20.
G. G Ning S. P Bai M. Z Bao L. Liu 《In vitro cellular & developmental biology. Plant》2007,43(2):95-100
Using immature embryos and cotyledons as explants, a successful system to culture immature embryos and induce direct regeneration
from cotyledons was established for Prunus mume “Xuemei”. For immature embryo culture, a high frequency of plantlet formation (89.5%) from the embryonic axis was obtained
using half-strength Murashige and Skoog (1/2 MS) medium supplemented with 13.2 μM 6-benzyladenine (BA) and 2.7 μM 1-naphthaleneacetic
(NAA). Shoots formed directly from cotyledons with the embryo axis intact when explants were cultured on 1/2 MS medium containing
2.2 μM BA with different combinations of NAA (2.7, 5.4 μM) and indole-3-butyric acid (IBA) (0, 2.5, 5.0 μM). Better results
were achieved when the embryonic axis was removed from the cotyledons and cultured on 1/2 MS medium supplement with 13.2 μM
BA, 2.7 μM NAA or 2.2 μM BA, 2.2 μM thidiazuron (TDZ), and 2.7 μM NAA, respectively. Regenerated shoots were successfully
rooted on 1/2 MS or Woody Plant medium (WPM) supplemented with 2.5–5.0 μM IBA. The effect of the embryonic axis, BA, and TDZ
on cotyledon regeneration was investigated in detail. Rooted plantlets were transferred to soil successfully. 相似文献