scholarly journals Construction of an RNAi vector for knockdown of GM-ACS genes in the cotyledonary nodes of soybean

2017 ◽  
Vol 26 ◽  
pp. 40-45
Author(s):  
Chunming Liu ◽  
Bowen Yang ◽  
Yuetong Ming ◽  
Jianfeng Liu ◽  
Yunqing Cheng
1997 ◽  
Vol 75 (3) ◽  
pp. 492-500 ◽  
Author(s):  
Delphine Popiers ◽  
Frédéric Flandre ◽  
Brigitte S. Sangwan-Norreel

In vitro regeneration of pea (Pisum sativum L.), a regeneration recalcitrant legume, was optimised using thidiazuron. Buds were initiated from the meristems of the cotyledonary nodes of embryo axes, isolated from mature seeds, and subcultured on Murashige and Skoog medium supplemented with 13.3 μM 6-benzylaminopurine, 16.1 μM α-naphthaleneacetic acid, and 0.2 μM 2,3,5-triiodobenzoic acid. Proliferation of buds was preceded by the formation of white nodular-like protrusions. These structures were cut transversally in fine slices and subcultured on the same medium or in presence of thidiazuron that produces a second wave of secondary budding. The best results (90–110 buds per expiant) were obtained with 10 μM thidiazuron. The capacity of regeneration was genotype independent and reproducible. Buds elongated on the initial medium, then formed roots in presence of 5.37 μM α-naphthaleneacetic acid. and developed into viable plants. Key words: Pisum sativum L., regeneration, meristems, embryo axes, thidiazuron.


2012 ◽  
Vol 63 (6) ◽  
pp. 570 ◽  
Author(s):  
P. Saravana Kumar ◽  
R. J. Lawn ◽  
L. M. Bielig

Amphicarpy, an adaptive trait whereby both aerial and underground fruits are formed on the one plant, occurs in several plant taxa, notably the Phaseoleae legumes. Amphicarpic species offer the dual potential benefits of enhanced persistence through their underground seed, combined with ease of harvest of their aerial seed. While amphicarpy has been reported in several endemic Australian tropical legumes, information on the trait is sparse. The objective of the current research was to compare aerial and underground reproductive structures in amphicarpic tropical legumes from four different sub-tribes within the Phaseoleae: three Australian endemic species, Vigna lanceolata (sub-tribe Phaseolinae), Flemingia pauciflora (sub-tribe Cajaninae), and Glycine falcata (sub-tribe Glycininae); and the exotic pasture legume Centrosema rotundifolium (sub-tribe Clitoriinae). As far as we know, this report of amphicarpy in F. pauciflora is the first record of the trait in a member of the Cajaninae. Descriptions, drawings, and photographs of the morphology and anatomy of the aerial and underground fruiting structures were documented. In general, the aerial flowers in all genotypes studied were chasmogamous, allowing at least some opportunity for outcrossing. In contrast, the underground flowers were invariably much reduced, with a small, non-pigmented corolla enclosed in much-reduced, scale-like sepals. Nonetheless, anthers and viable pollen were observed in the underground flowers in all four species. With the exception of C. rotundifolium, the underground fruiting structures formed on rhizomes which initially arose either from the underground cotyledonary nodes or, in the case of G. falcata, which is epigeal, from the junction of the stem and taproot. The rhizomes gave rise to ramets when they emerged at the surface or from holes in pot bases. The V. lanceolata accessions also produced fleshy tubers which gave rise to rhizomes, especially in subsequent years. In C. rotundifolium, the geocarpic structures arose on specialised, fleshy, geotropic stems that grew down from the stoloniferous stems. In all species, the number of seeds per underground pod was fewer than in the aerial pods, and the underground seeds were invariably larger, although the extent differed between legume genotypes. There was no evidence of effects on growth or development depending on whether plants were grown from aerial or underground seeds. Some of the adaptive and agronomic implications of the key findings are discussed. In particular, it is argued that amphicarpy in the Australian species is an adaptation to seed predation, and to spatially heterogeneous inland soils.


Author(s):  
S. Parvin ◽  
M. Kausar ◽  
M. Enamul Haque ◽  
M. Khalekuzzaman ◽  
B. Sikdar ◽  
...  

A rapid and efficient protocol is outlined for in vitro propagation of muskmelon(Cucumis melo L.) Shoot tips, nodal segments and cotyledonary nodes from invitro grown seedlings were used as explants. The explants were inoculated on MS medium fortified with different combinations and concentrations of growthregulators viz., BAP, NAA, GA3 and IBA for multiple shoot regeneration.Effective result was found on MS medium supplemented with 2.0 mg/l BAP, inwhich 90% and 70% cultures induced multiple shoots from nodal segments andshoot tip explants, respectively. Whereas, 70% cultures of cotyledonary nodeswere found to induced shoots on MS medium with 1.5 mg/l BAP + 0.1 mg/l GA3. In vitro regenerated shoots were subcultured on half strength MS mediumsupplemented with different concentrations of IBA and NAA for successful rootinduction and the effective result (up to 70%) was found in medium with 1 mg/lIBA. Well rooted in vitro grown plantlets were acclimatized in sandy soil, whereas 70% plantlets survived


Plants ◽  
2020 ◽  
Vol 9 (3) ◽  
pp. 318
Author(s):  
Mehtab Muhammad Aslam ◽  
Joseph K. Karanja ◽  
Qian Zhang ◽  
Huifeng Lin ◽  
Tianyu Xia ◽  
...  

The tissue culture regeneration system of Lupinus albus has always been considered as recalcitrant material due to its genotype-dependent response and low regeneration efficiency that hamper the use of genetic engineering. Establishment of repeatable plant regeneration protocol is a prerequisite tool for successful application of genetic engineering. This aim of this study was to develop standardized, efficient protocol for successful shoot induction from cotyledonary node of white lupin. In this study, 5 day old aseptically cultured seedlings were used to prepare three explants (half cotyledonary node, HCN; whole cotyledonary node, WCN; and traditional cotyledonary node, TCN), cultured on four concentrations of M519 medium (M519, ½ M519, 1/3 M519, and ¼ M519), containing four carbohydrate sources (sucrose, fructose, maltose, and glucose), and stimulated with various combinations of KT (kinetin), and NAA (naphthalene acetic acid) for direct shoot regeneration. High frequency of 80% shoot regeneration was obtained on ½ M519 medium (KT 4.0 mg L−1 + NAA 0.1 mg L−1) by using HCN as an explant. Interestingly, combinations of (KT 4.0 mg L−1 + NAA 0.1 mg L−1 + BAP 1.67 mg L−1), and (KT 2.0 mg L−1 + NAA 0.1 mg L−1) showed similar shoot regeneration frequency of 60%. Augmentation of 0.25 g L−1 activated charcoal (AC) not only reduced browning effect but also improved shoot elongation. Among the all carbohydrate sources, sucrose showed the highest regeneration frequency with HCN. Additionally, 80% rooting frequency was recorded on ½ M519 containing IAA 1.0 mg L−1 + KT 0.1 mg L−1 (indole acetic acid) after 28 days of culturing. The present study describes establishment of an efficient and successful protocol for direct plant regeneration of white lupin from different cotyledonary nodes.


2016 ◽  
Vol 41 (3) ◽  
pp. 521-528
Author(s):  
MR Kabir ◽  
S Ahmed ◽  
MAY Akhond

Seedling-derived cotyledonary nodes and hypocotyl explants of BARI Dherosh- 1 were cultured in vitro on MS medium supplemented with varying concentrations of 2, 4-Dichlorophenoxy acetic acid (2, 4-D), 6- Benzylaminopurine (BAP), Thidiazuron (TDZ), BAP with 1-Nepthaleneacetic acid (NAA), BAP with Indole 3-butyric acid (IAA) and Zeatin with IAA along with a control. Shooting response (100%) with callus was only observed from cotyledonary nodes on thidiazuron (TDZ) where hypocotyls produced only callus or callus with roots on different concentrations of plant growth regulators. Considering the shooting response, the cotyledonary nodes of BARI Dherosh-1 were cultured on various concentrations of TDZ for regeneration. The highest percentage (64.0) with maximum number (6.8) of shoots per explant were observed in 0.044 ?M TDZ in 8.4 days. The regenerated shoots were rooted on ½ strength MS, MS supplemented with 2.46 ?M IBA and 0.53 ?M NAA. The highest percentage (83.3) and minimum days (9.7) required for root induction were recorded in 2.46 ?M IBA. The rooted plantlets were transferred to soil and hardened in the plastic pots under green house conditions. The rooted shoots grew normally under natural conditions following acclimatization.Bangladesh J. Agril. Res. 41(3): 521-528, September 2016


1975 ◽  
Vol 53 (9) ◽  
pp. 921-928 ◽  
Author(s):  
James E. Rahe ◽  
Robert M. Arnold

Phaseollin accumulated locally at point-freezing injuries on hypocotyls of intact etiolated seedlings of Phaseolus vulgaris. Maximum amounts occurred within 24 to 30 h after injury. Smaller amounts accumulated at similar sites on hypocotyls excised at the time point-freezing injuries were made, and the accumulation was less localized. Increasing amounts of phaseollin occurred at sites increasingly distant from the cotyledonary nodes in both intact and excised hypocotyls. Much higher levels of phaseollin were elicited by excision per se than by point-freezing. Phaseollin was not detected after freezing of whole hypocotyls, indicating that living tissue adjacent to injuries is required for accumulation. The data are discussed in relation to host–parasite specificity, with particular reference to the interaction between P. vulgaris and Colletotrichum lindemuthianum.


1975 ◽  
Vol 53 (3) ◽  
pp. 243-248 ◽  
Author(s):  
Carol A. Peterson ◽  
R. A. Fletcher

Lateral buds at the cotyledonary nodes of soybean plants grown under the conditions used in this study usually remain inhibited. These buds grow when the apical part of the plant is removed. They will grow, but less strongly, when the roots as well as the apex of the plant are removed and the basal end of the cut stem is placed in a mineral salt solution. Bud growth is further diminished by decreasing the length of stem left attached to the bud. The cotyledon is essential for bud growth on plant segments maintained in nutrient solution, but it can be replaced by a 1% sucrose solution during the early days of bud growth. Buds which are completely detached from the stem and placed in 1% sucrose do not elongate, but a small number of cell divisions are detectable, indicating that the early events of the release from inhibition have occurred. Buds elongate when they are apically or centrally located on stem segments. Increasing the length of the attached stem segments increases the growth of the buds. Additions of the cytokinin benzyladenine to plants causes a dramatic increase in bud growth when buds are attached to stem segments but does not stimulate growth of buds without stem segments. It is concluded that benzyladenine alone will not substitute for a factor(s) present in the stem which is necessary for bud growth. Increasing stem lengths above buds located at the basal ends of segments inhibits bud growth. It is suggested that this may be due to an accumulation of endogenous auxin at the site of the buds.


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