scholarly journals Hormone-injected leaf cutting, a new efficient in vivo multiplication protocol for two succulent plants

Author(s):  
Xiaodan Xu ◽  
Wei Zheng

This study aimed to establish a simple and efficient in vivo multiplication protocol by leaf cutting to satisfy the supply of young succulent ornamentals Pachyveria pachytoides and Sedum morganianum. The regenerability of leaves injected with 6-benzylaminopurine (BAP) and α-naphthalene acetic acid (NAA) in vivo were tested with common leaf cutting as control. Results showed a 100% shoot induction frequency using hormone-injeceted methods for the two species. The number of shoots per leaf of 4.0 or 6.0 mg l −1 BAP and 0.1 mg l −1 NAA injected in vivo (5.08-5.14 in P. pachytoides, and 6.22-6.74 for S. morganianum) were significantly greater than that of the other treatments. Since the h ormone-injected leaf cutting needs no aseptic operation which is necessary for in vitro multiplication, it is simple for the commercial production of the two species. The new in vivo propagation method would be of great interest for growers and breeders of succulent plants.

2017 ◽  
Author(s):  
Xiaodan Xu ◽  
Wei Zheng

This study aimed to establish a simple and efficient in vivo multiplication protocol by leaf cutting to satisfy the supply of young succulent ornamentals Pachyveria pachytoides and Sedum morganianum. The regenerability of leaves injected with 6-benzylaminopurine (BAP) and α-naphthalene acetic acid (NAA) in vivo were tested with common leaf cutting as control. Results showed a 100% shoot induction frequency using hormone-injeceted methods for the two species. The number of shoots per leaf of 4.0 or 6.0 mg l −1 BAP and 0.1 mg l −1 NAA injected in vivo (5.08-5.14 in P. pachytoides, and 6.22-6.74 for S. morganianum) were significantly greater than that of the other treatments. Since the h ormone-injected leaf cutting needs no aseptic operation which is necessary for in vitro multiplication, it is simple for the commercial production of the two species. The new in vivo propagation method would be of great interest for growers and breeders of succulent plants.


2015 ◽  
Vol 22 (1) ◽  
pp. 33-36
Author(s):  
A. Benniamin ◽  
G. Jothi ◽  
M. Sundari

Protocols of axillary bud multiplication were established for Dodonaea viscosa (Sapindaceae). Murashig & Skoog’s medium with 0.2 mg/l BAP with 0.01 Naphthalene acetic acid induced high rate of shoot induction and an average of five shoots per node. Subsequent culture enhanced the number of shoots. Callus initiated from the basal cut end explants differentiated in to more than 10 shoots on MS Medium with 0.4mg/l Benzylaminopurine and 0.02mg/l Indole Butric Acid. Eighty per cent of the rooted shoots survived when transferred to greenhouse and subsequently to the field.


2012 ◽  
Vol 7 (4) ◽  
pp. 698-707 ◽  
Author(s):  
Ely Zayova ◽  
Ira Stancheva ◽  
Maria Geneva ◽  
Maria Petrova ◽  
Rumiana Vasilevska-Ivanova

AbstractAn effective in vitro protocol for rapid clonal propagation of Echinacea purpurea (L.) Moench through tissue culture was described. The in vitro propagation procedure consisted of four stages: 1) an initial stage - obtaining seedlings on Murashige and Skoog (MS) basal medium with 0.1 mg L−1 6-benzylaminopurine, 0.1 mg L−1 α-naphthalene acetic acid and 0.2 mg L−1 gibberellic acid; 2) a propagation stage — shoot formation on MS medium supplemented with 1 mg L−1 6-benzylaminopurine alone resulted in 9.8 shoots per explant and in combination with 0.1 mg L−1 α-naphthalene acetic acid resulted in 16.2 shoots per explant; 3) rooting stage — shoot rooting on half strength MS medium with 0.1 mg L−1 indole-3-butyric acid resulted in 90% rooted microplants; 4) ex vitro acclimatization of plants. The mix of peat and perlite was the most suitable planting substrate for hardening and ensured high survival frequency of propagated plants. Significant higher levels were observed regarding water-soluble and lipid-soluble antioxidant capacities (expressed as equivalents of ascorbate and α-tocopherol) and total pnenols content in extracts of Echinaceae flowers derived from in vitro propagated plants and adapted to field conditions in comparison with traditionally cultivated plants.


2016 ◽  
Vol 47 (3) ◽  
Author(s):  
AL-Hamidawi & Hamad

This research was conducted at the plant tissue culture Lab. College of Agriclture, University of Baghdad from February to October 2015. The aim of the study was investigate the  influence of light quality and Naphthalene  Acetic Acid(NAA) on some properties of roots for two varieties Martinque and Yanara shoots of Gerbera jamesonii, cultured on MS medium supplemented with 0.3 mg.L -1 Spermidine. The results indicated that 1/2 MS medium with free auxin NAA gave the highest percentage of rooting (75 %) Which differed significantly from the other concentrations of NAA. White light gave the hightest percentage of rooting (89 %), that was not significantly different from the red  light (78%) . While the treatment of Martinque variety under White light gave the highest percentage of rooting (100%), that was not significantly different from Yanara variety that gave (78%). MS medium with free auxin NAA gave the highest number of roots (7.5 % root/shoot ) that was significantly different on all the other concentrations of NAA. MS medium with free auxin NAA under White light of roots (6.6 root/shoot) at Martinque variety . While MS medium with free auxin NAA under blue light gave the highest number of roots (10.10 roots/shoot) that was not different significantly from red light it gave (8.9 root/shoot) Martinque variety gave the highest rate of root length ( 1.62 cm) Which not differend  significantly from Yanara variety it gave (1.49 cm) While The treatment of Martinque variety under White light with NAA- free medium gave the highest rate of root length (3.40 cm) and was significantly different on all the other interactions


1969 ◽  
Vol 23 (3) ◽  
pp. 567-583 ◽  
Author(s):  
J. D. Sutton

1. Studies were made of the fermentation of D-glucose, D-fructose, D-galactose, D-xylose, L-arabinose and sucrose by rumen contents from two cows fed 1 kg hay and 4 or 5 kg flaked maize once daily. The proportions of volatile fatty acids (VFA) in the rumen before addition of carbohydrates varied widely but on average acetic acid constituted about 52%, propionic acid about 29% and n-butyric acid about 13% of the total.2. In in vitro experiments, 896 mg of the monosaccharides and 851 mg sucrose were added to 150 g mixed rumen contents incubated for 2 h; the carbohydrates were added at 10 min intervals throughout the incubation on three occasions with each cow. Mean proportions of the carbohydrates fermented ranged from about 60% of the pentoses to about 85% of sucrose and glucose. Of the VFA produced from galactose and the pentoses, acetic acid constituted about 40%, propionic acid 45–55% and n-butyric acid 1–7%; very little n-valeric acid was produced. With the other carbohydrates results from the two cows differed, owing mainly to the production of appreciable amounts of n-valeric acid with one cow only. Acetic acid constituted about 40% of the VFA produced from fructose and sucrose, propionic acid 20–40%, n-butyric acid 14–22% and n-valeric acid up to 12%. The proportions of VFA produced from glucose were intermediate between the other two groups.3. Net recovery of carbon from fermented carbohydrate in VFA was about 35–45%. A further 1–6%, of fermented glucose, fructose and sucrose was recovered in lactic acid.4. In in vivo experiments, the monosaccharides only were infused into the rumen for 8 h at the rate of 200 g/h. Changes in the concentrations of substrates and products varied widely, owing to the variable basal fermentation, but changes in the proportions of VFA in the rumen were similar to those found in vitro.5. The results of the in vitro experiments were compared with those obtained in earlier experiments in which the same cows were given a diet containing 70% hay. Significant regressions (P < 0.05) were found between the molar proportions of acetic, propionic and n-valeric acids produced from the substrates and the proportions of these acids present in the rumen contents at the start of the incubations, but the relationships differed markedly among the different carbohydrates. Most of the significant regressions were positive but negative regressions for propionic acid production from fructose and sucrose with one cow suggested the existence of more complex interrelationships among two or more VFA.


1973 ◽  
Vol 29 (02) ◽  
pp. 490-498 ◽  
Author(s):  
Hiroh Yamazaki ◽  
Itsuro Kobayashi ◽  
Tadahiro Sano ◽  
Takio Shimamoto

SummaryThe authors previously reported a transient decrease in adhesive platelet count and an enhancement of blood coagulability after administration of a small amount of adrenaline (0.1-1 µg per Kg, i. v.) in man and rabbit. In such circumstances, the sensitivity of platelets to aggregation induced by ADP was studied by an optical density method. Five minutes after i. v. injection of 1 µg per Kg of adrenaline in 10 rabbits, intensity of platelet aggregation increased to 115.1 ± 4.9% (mean ± S. E.) by 10∼5 molar, 121.8 ± 7.8% by 3 × 10-6 molar and 129.4 ± 12.8% of the value before the injection by 10”6 molar ADP. The difference was statistically significant (P<0.01-0.05). The above change was not observed in each group of rabbits injected with saline, 1 µg per Kg of 1-noradrenaline or 0.1 and 10 µg per Kg of adrenaline. Also, it was prevented by oral administration of 10 mg per Kg of phenoxybenzamine or propranolol or aspirin or pyridinolcarbamate 3 hours before the challenge. On the other hand, the enhancement of ADP-induced platelet aggregation was not observed in vitro, when 10-5 or 3 × 10-6 molar and 129.4 ± 12.8% of the value before 10∼6 molar ADP was added to citrated platelet rich plasma (CPRP) of rabbit after incubation at 37°C for 30 second with 0.01, 0.1, 1, 10 or 100 µg per ml of adrenaline or noradrenaline. These results suggest an important interaction between endothelial surface and platelets in connection with the enhancement of ADP-induced platelet aggregation by adrenaline in vivo.


1987 ◽  
Vol 52 (9) ◽  
pp. 2317-2325 ◽  
Author(s):  
Jan Hlaváček ◽  
Jan Pospíšek ◽  
Jiřina Slaninová ◽  
Walter Y. Chan ◽  
Victor J. Hruby

[8-Neopentylglycine]oxytocin (II) and [8-cycloleucine]oxytocin (III) were prepared by a combination of solid-phase synthesis and fragment condensation. Both analogues exhibited decreased uterotonic potency in vitro, each being about 15-30% that of oxytocin. Analogue II also displayed similarly decreased uterotonic potency in vivo and galactogogic potency. On the other hand, analogue III exhibited almost the same potency as oxytocin in the uterotonic assay in vivo and in the galactogogic assay.


2009 ◽  
Vol 36 (No. 4) ◽  
pp. 140-146 ◽  
Author(s):  
J.K. Kanwar ◽  
S. Kumar

The influence of growth regulators, explants and their interactions on in vitro shoot bud formation from callus was studied in <I>Dianthus caryophyllus</I> L. The leaf and internode explants were cultured on Murashige and Skoog (MS) medium containing different concentrations of growth regulators. The highest callus induction was observed with 2 mg/l 2,4-dichlorophenoxy acetic acid (2,4-D) and 1 mg/l benzyl adenine (BA). Out of twenty seven shoot regeneration media tested, only 2 mg/l thidiazuron (TDZ) and zeatin alone or in combination with naphthalene acetic acid (NAA) and/or indole acetic acid (IAA) could differentiate calli. The highest average number of shoots was observed with 2 mg/l TDZ and 1 mg/l IAA. Significant differences were observed in calli producing shoots and number of shoots per callus in the explants of leaf and internode. The shoots were elongated and multiplied on MS medium supplemented with 1 mg/l BA and solidified with 1% agar. The shoots were rooted and hardened with 76% survival success in pots after six weeks of transfer to the pots.


Author(s):  
Thriveni Vasanth Kumar ◽  
Manjunatha H. ◽  
Rajesh Kp

Objective: Dietary curcumin and capsaicin are well known for their health beneficial potencies. The current study was done to assess the anti-inflammatory activity of curcumin, capsaicin and their combination by employing in vitro and in vivo models.Methods: We investigated the protective effect of curcumin, capsaicin and their combination using in vitro heat induced human red blood cell (HRBC) membrane stabilisation, in vivo 3% agar induced leukocyte mobilisation and acetic acid induced vascular permeability assay.Results: Curcumin, capsaicin and their combination exhibited concentration dependent protective effect against heat-induced HRBC membrane destabilisation, while combined curcumin and capsaicin restored 87.0±0.64 % membrane stability and it is found to be better than curcumin, capsaicin and diclofenac sodium (75.0±0.25. 72±0.9 and 80.0±0.31 %) protective effect. In agar suspension induced leukocyte mobilization assay, the combined curcumin and capsaicin had shown 39.5±1.58 % of inhibition compared to individual curcumin and capsaicin, which showed moderate inhibition of 16.0±3.14 and 21.6±2.17 % respectively. Besides, the combined curcumin and capsaicin had shown highly significant inhibition of acetic acid-induced vascular permeability in rats (62.0±3.14 %), whereas individual curcumin and capsaicin showed moderate inhibition of vascular permeability with 36.0±2.41 and 43.0±1.92 % respectively.Conclusion: This study demonstrates the significant anti-inflammatory property of combined curcumin and capsaicin at half of the individual concentration of curcumin and capsaicin.


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