Recalcitrant Genotypes Research Articles

A new approach for efficient regeneration of a recalcitrant genotype of sunflower ( Helianthus annuus ) by organogenesis induction on split embryonic axes

A new approach for shoot regeneration from split embryonic axes of Helianthus annuus var. RHA266, a poor responding genotype to in vitro culture, has been developed. The regeneration procedure is based on successive excision of the apical and axillary shoots originating from pre-existing meristems. This elimination process stimulates adventitious shoot bud formation in 80% of treated explants. Although newly induced buds were observed on hormone-free medium, higher rate of induction and bud development were obtained on medium containing 0.1 mg l−1 BA. All regenerated plants were phenotypically similar to seed-derived RHA 266 plants with no observed somaclonal variation, as assessed by AFLP analysis. The efficient shoot regeneration from newly formed meristematic cells should offer opportunities to genetically engineer economically important sunflower genotypes that have proven till now, to be recalcitrant towards other regeneration systems.

Putrescine-enhanced somatic embryos and plant numbers from elite oat (Avena spp. L.) and reciprocal crosses

Mature embryos from hulled, regenerable GP-1 (A. sativa L.), hull-less, recalcitrant Tibor (A. nuda L.) and reciprocal crosses were cultured in vitro on a putrescine- (Put) containing medium. Hormone-free Murashige and Skoog medium (MS-0) or shoot proliferation medium (SPM) [2.0 mgl−1 (9.0 μM) 2,4-dichlorophenoxyacetic acid (2,4-D)], with and without 0.5 mM Put or 1 mM Put, were tested for effects on somatic embryogenesis and plant regeneration. Put/SPM (0.5mM) was the best medium for both somatic embryos (SEs) and plant numbers per gram of callus, regardless of genotype. This effect was most evident in Tibor, which produced no somatic embryos or plants on SPM, a previously published regeneration medium, and in Tibor ×GP-1, which produced reduced numbers of SE and plants on the remaining media. The number of SEs per gram of callus for GP-1 and GP-1× Tibor showed little significant differences between the different media. Put treatments produced plants from the four genotypes but the regeneration efficiency on Put-containing medium was similar or even better than on SPM for explants containing maternal GP-1 germplasm. This suggests that Put-containing MS-0 medium can be used for testing regeneration of other oat lines. In addition, SPM containing 0.5 mM Put can be used to induce significant regeneration of plants from normally recalcitrant genotypes. This improvement greatly increases the number of potential germplasms for further transformation efforts.

The effect of ovary-conditioned medium on microspore embryogenesis in common wheat (Triticum aestivum L.)

Microspores were isolated from wheat (Triticum aestivum L.) spikes of various genotypes following an effective pretreatment that induced microspore embryogenesis. The isolated microspores were cultured with or without live ovaries, and with or without medium pre-conditioned by ovaries for varying periods of time. Live ovaries alone increased androgenic embryoid yields up to 4.5-fold over the control for microspores isolated from responsive genotypes. While live ovary co-culture alone was not effective for microspores isolated from recalcitrant genotypes, the addition of medium preconditioned by ovaries to microspore cultures increased embryoid yield by more than 100-fold. Without ovary-conditioned medium, no embryoids could be obtained from some recalcitrant genotypes. Ovary-conditioned medium apparently functions to increase embryoid yields by providing essential substance(s) for elaboration of the embryogenic program already triggered during pretreatment.

Enhancement of microspore culture efficiency of recalcitrant barley genotypes

The culture response of isolated microspores of seven recalcitrant cultivars of barley has been largely improved by identifying an appropriate pretreatment and utilizing ovary co-cultivation. After comparison of three pretreatment media, medium B was shown to be most efficient for inducing microspore embryogenesis, while 0.3 M mannitol frequently used for the responsive cv. Igri was found to be ineffective for recalcitrant genotypes. A further significant improvement of embryogenesis was achieved by using ovary co-culture, which resulted in an overall 2.1-fold increase in embryo formation and 2.4-fold increase in green plant regeneration from all cultivars compared with the control. Optimal co-culture conditions were identified as 5 ovaries/ml medium kept over 20 days in induction culture. Microspore plating densities in cultures with and without co-culture were found to be optimal at 4×104/ml and 8–12×104/ml, respectively. The most effective and reproducible method for culturing microspores of recalcitrant genotypes appeared to be the combination of medium B pretreatment with ovary co-culture. By using this procedure, the genotypic difference in microspore embryogenesis could be reduced. It was found that medium B mainly enhanced percent live embryogenic microspores, and ovary co-culture subsequently improved cell division and embryogenic development. The method described here is important for the application of the microspore culture technique to barley breeding and biotechnology.

Competence of Arabidopsis thaliana genotypes and mutants for Agrobacterium tumefaciens-mediated gene transfer: role of phytohormones.

Many plant species and/or genotypes are highly recalcitrant to Agrobacterium-mediated genetic transformation, and yet little is known about this phenomenon. Using several Arabidopsis genotypes/ecotypes, the results of this study indicated that phytohormone pretreatment could overcome this recalcitrance by increasing the transformation rate in the known recalcitrant genotypes. Transient expression of a T-DNA encoded ss-glucuronidase (GUS) gene and stable kanamycin resistance were obtained for the ten Arabidopsis genotypes tested as well as for the mutant uvh1 (up to 69% of petioles with blue spots and up to 42% resistant calli). Cultivation of Arabidopsis tissues on phytohormones for 2-8 d before co-cultivation with Agrobacterium tumefaciens significantly increased transient GUS gene expression by 2-11-fold and stable T-DNA integration with petiole explants. Different Arabidopsis ecotypes revealed differences in their susceptibility to Agrobacterium-mediated transformation and in their type of reaction to pre-cultivation (three types of reactions were defined by gathering ecotypes into three groups). The Arabidopsis uvh1 mutant described as defective in a DNA repair system showed slightly lower competence to transformation than did its progenitor Colombia. This reduced transformation competence, however, could be overcome by 4-d pre-culture with phytohormones. The importance of pre-cultivation with phytohormones for genetic transformation is discussed.

Cultural Conditions Affecting the Frequency of Embryoid Formation in Sweetpotato (Ipomoea batatas)

Somatic embryogenesis in sweetpotato is highly genotype dependent. Unfortunately, many desirable agronomic varieties do not produce embryos capable of germination when published protocols are followed. Using one responsive and three recalcitrant cultivars, we examined the effect on embryogenesis of auxin, nitrogen, and carbon; explant source; and desiccation. All cultivars formed proembryonic masses on medium supplemented with either 2,4-D or picloram; picloram favored the growth of nonembryogenic callus. Twenty mm each of ammonium and nitrate promoted the best proembryo formation in all cultivars. Ammonium was essential for embryogenesis; replacing ammonium with proline, glutamine, asparagine, glycine, or casein hydrolysate resulted in poor or no proembryo formation. More proembryos formed on medium supplemented with sucrose than with glucose, fructose, or maltose. Leaf discs from the first fully expanded leaf produced more embryos than younger leaves for all cultivars; discs taken from the lamina produced more embryos than discs including portions of the midrib. Proembryos matured and germinated only after at least 3 weeks on medium containing 5% w/v polyethylene glycol 8000, greater than 3.3 mm myo-inositol, and 1 or 10 μm abscisic acid. More whole plants were obtained from the responsive cultivar Jewel than from the recalcitrant genotypes.

Predictive correlates of shoot regeneration from potato protoplast culture

Adaptation of protoplast regeneration systems for use on untested or recalcitrant potato genotypes can be a time-consuming exercise. Callus growth and xylogenesis were evaluated as early correlates of shooting potential to shorten this process. Callus growth was of limited value for predicting organogenesis but a linear relationship was observed between xylogenesis and shooting frequency. Increases in xylem content above a minimum threshold corresponded with increases in shooting frequency. The predictive value of the relationship was tested using a simple protocol modification (the culture of calli on a filter paper base). Calli on filter paper produced more xylem elements and shoots than those plated directly on medium. The potential of xylem content as a predictive test of shooting frequency is discussed.

Screening Pyrus Germplasm for in Vitro Rooting Response

Micropropagated shoots of 49 Pyrus species and cultivars and one selection of Pyronia veitchii (Trabut) Guillaumin were evaluated to test their responses to several in vitro rooting techniques. Auxin treatment was required for rooting in most cases. Eighteen of 50 accessions rooted ≥50% with a 15-second, 10-mm IBA dip followed by growth on medium with no growth regulators (NGR). Twelve accessions rooted on a medium with 10 μm IBA applied for 1 week followed by NGR medium for 3 weeks; NGR medium alone was effective for only two accessions. Twenty-eight accessions rooted poorly with IBA treatments; an additional treatment of a 15-second dip in 10 mm NAA followed by NGR medium produced ≥50% rooting for eight genotypes. Root production increased for 10 of 19 especially recalcitrant genotypes by 10 μm IAA treatments in darkness or at 30C and NAA dip treatments. Of rooted shoots, 73% survived acclimation in the greenhouse. Selections of Pyrus betulifolia Bunge, P. calleryana Decne., P. hondoensis Kikuchi and Nakai, P. koehnei C. Schneider, P. pashia Buch.-Ham. ex D. Don, P. pyrifolia (Burm.f.) Nakai cv. Shinseiki, P. regelii Rheder, P. ussuriensis Maxim., and the Pyronia veitchii selection failed to root in any of the treatments. Twenty-five of 32 P. communis L. cultivars and three other species rooted on at least one of the treatments. Chemical names used: 1-naphthaleneacetic acid (NAA), 1H-indole-3-butyric acid (IBA), 1H-indole-3-acetic acid (IAA).

Endogenous polyamine content during in vivo maturation and in vitro culture of maize pollen

Changes in polyamine content during in vivo maturation and in vitro culture of maize (Zea mays L.) pollen were studied. The endogenous content of free, conjugated and bound polyamines was analyzed during 30 days of pollen evolution, in both developmental pathways (microsporogenesis and androgenesis). The induction of androgenesis from cold-pretreated uninucleate pollen results, in most of cases, in a lower total polyamine content than that of the in vivo uninucleate pollen. These differences indicate that polyamine metabolism is altered during the induction of androgenesis, and this could be a consequence of increased polyamine assimilation. In general, pollen stages that involve cell division (tetrades, pre-anthesis pollen and four-day cultured pollen) are characterized by a predominance of free Spd. The increase of Spd and Spm in 15-day cultured pollen, when the first embryoids are formed, outline the possible implication of these polyamines in embryogenetic processes. Furthermore, these findings may contribute to the improvement of maize androgenesis yield, especially in recalcitrant genotypes, by the exogenous application of polyamines or polyamine-inhibitors to the culture medium.

Changes in free radical profiles during the callogenesis of responsive and recalcitrant potato genotypes

Changes of the in vitro morphogenetic state may be achieved for some potato genotypes, but others are unresponsive (recalcitrant). Although the biochemical basis for somatic recalcitrance is unknown, evidence suggests that two different aspects of oxidative stress may be involved. Phenolic oxidation is a major problem in manipulating cultures of woody plant species (Thorpe & Harry 1990) and lipid peroxidation has been associated with recalcitrance in monocotyledonous plants (Cutler et al. 1989; Benson et al. 1992). Both oxidative phenomena are believed to be free-radical mediated, but to date there is no reported direct evidence for the formation of free radicals during plant tissue culture callogenesis. The objectives of the present study were twofold; to assess the feasibility of using electron paramagnetic resonance (EPR) spectroscopy to detect free radicals directly in plant tissue cultures and to investigate free radical activity during dedifferentiation of responsive and unresponsive potato genotypes.

Effect of experimental conditions and genotypic variability on somatic embryogenesis in Coffea arabica

The somatic embryogenic potential of leaf explants from greenhouse-grown plants of eight Coffea arabica genotypes was investigated on three different gelose-gelled culture media (Dublin, Pierson, and Yasuda). Four of these genotypes were reactive. Optimal somatic embryogenesis was obtained when the explants were taken from microcutting and cultured on gelrite-gelled Yasuda's medium. Under these culture conditions, somatic embryos and plantlets were obtained in two previously recalcitrant genotypes. The histocytological callus development was found to be identical in responsive or recalcitrant genotypes. Embryogenic cells formed at two successive points during callogenesis and their subsequent development varied according to culture conditions. Cells initiated in 10- to 15-day-old calli either degenerated or developed directly into embryos. Cells initiated in 60-day-old calli became isolated and developed into embryos or their development was arrested. Embryos obtained in these conditions were able to develop into plantlets. Key words: Coffea arabica, genotypic variability, histocytology, in vitro culture, somatic embryogenesis.

Comparison of media for their aptitude in wheat anther culture

Different media were evaluated with anthers of five spring wheat (Triticum aestivum L.) genotypes for their ability to produce embryos and green plants in anther culture. Our first experiment showed that the addition of a combination of 19 amino acids significantly increased the number of embryos and green plants obtained. The mean number of green plants per 100 anthers for the two genotypes in this experiment, HY320 and B723, went from 28.2 without amino acids in the medium, to 46.7 with addition of amino acids. Our second experiment with the genotypes HY320, Wim and Laval-19 showed that liquid medium with Ficoll is more efficient for anther culture (9.9 green plants/100 anthers) than solid (0 green plants), gelationous media (2.5 green plants/100 anthers) or liquid medium with Membrane Rafts (0 green plants; Hoechst Celanese Corp.). Our third experiment revealed that the effect of replacement of sucrose by maltose varied with the genotype of the donor plant. Maltose partially inhibited the androgenesis of three responsive genotypes, HY320, Wim and Reliance (40.3 green plants/100 anthers instead of 43.9 with sucrose), while maltose significantly increased the androgenesis of the recalcitrant genotype Laval-19 (10.8 green plants/100 anthers instead of 5.4 with sucrose). An amino acid x maltose interaction was also observed. Amino acids without maltose increased androgenesis, but the addition of maltose to the amino acid-enriched medium eliminated this positive effect of the amino acids.

Protoplast culture and plant regeneration of different agronomically important Brassica species and varieties

Protoplast cultures were prepared from 6-day-old hypocotyls of six spring, seven winter cultivars of Brassica napus L. and one line of Brassica campestris L. The molarity of enzyme solution was raised to 0,714 M mannitol resulting in well manipulable, cytoplasm dense protoplasts. In the protoplast purification procedure density gradient centrifugation was used to minimize physical damage of protoplasts. Three different protoplast culture systems —(1) liquid, (2) 2nd day embedded, (3) directly embedded in low melting agarose were compared. The two different protoplast embedding techniques resulted in the same efficiency of cell division as the liquid culture method and over this fact the colony browning was avoided. Using protoplast agarose-embedding and culture techniques, healthy calli were obtained for plant regeneration experiments. Incorporation of silver nitrate into the regeneration medium improved the efficiency of plant regeneration in responsive genotypes and the regeneration was induced in three nonresponsive (without silver nitrate) genotypes, too. The supplement of silver nitrate in regeneration medium was especially advantageous in plant regeneration of B. campestris. Out of fourteen commercial cultivars of Brassica napus and B. campestris, there is only one recalcitrant genotype in obtaining plantlets from protoplast-derived calli.

Medium‐Genotype‐Interaction on Androgenetic Haploid Production in Wheat

AbstractThe present study investigates the effects of media on the rate of green plantlet formation from anther cultures of five different winter and spring wheat cultivars. An increased number of embryos and calli were produced on Ficoll‐containing liquid potato‐2 medium, whereas the addition of 0.2 M/l maltose increased the rate of regeneration. The genotypes had strong effect on the formation of plantlets, but the developed procedure allows also the regeneration of recalcitrant genotypes. On the best medium sequence, a total of 2430 anthers over all genotypes were plated which developed 1325 macroscopic structures (55 %) of which 159 green plants have developed, i.e. 12 % from the structures and 7 % from the plated anthers, respectively.

Effects of donor plant environment and light during incubation on anther cultures of some spring wheat (Triticum aestivum L.) cultivars

Four different growth environments (field, two phytotron greenhouses and one growth chamber) were compared, using two genotypes of spring wheat, one recalcitrant and one responsive. Field-grown plants gave inferior results. Large improvements could be made by improving the conditions, embryoid frequencies in the two genotypes reaching 77.1% and 183.9% per 100 anthers, respectively. High light intensity during the induction phase strongly suppressed induction in both genotypes, but stimulated regeneration of green plants in the recalcitrant genotype, which had the lowest regeneration ability. Weak, diffuse light did not inhibit induction while the positive effect on regeneration was maintained. Also, another recalcitrant genotype was grown in the field, together with two F1-hybrids (recalcitrant x recalcitrant and recalcitrant x responsive). Evidence for a three-factor system was obtained.

Genetic and physiological influences on differentiation in tissue cultures of a legume, Lathyrus sativus

Callus initiation and subsequent organogenetic potential in cultures of shoot meristems of Lathyrus sativus is under genetic control. This genetic influence is observable not only at the broader intercultivar level, but also between genotypes descended from the same cultivar. However, it is possible to achieve higher levels of morphogenetic response even in recalcitrant genotypes by using the physiologically altered explant. On activation of the dormant lateral bud meristems consequent to decapitation of the apical bud, it is possible to induce organogenesis in the tissues of all genotypes. Callus masses arising from the shoot meristems and leaf expiants of cv. 'LSD-3' also exhibit somatic embryogenesis which results in the development of mature plantlets under culture conditions.

Short Communication: In vitro response of papaya (Carica papaya) to plant growth regulators

Abstract. Teixeira da Silva JA. 2016. In vitro response of papaya (Carica papaya) to multiple plant growth regulators. Nusantara Bioscience 8: 77-82. The use of plant growth regulators (PGRs) in papaya (Carica papaya L.) tissue culture is essential for tissue and organ culture in vitro. In this study, in a bid to expand the information available on the response to PGRs, a wide range of PGRs, roughly divided into four groups (auxins, cytokinins, alternative PGRs, growth inhibitors, and retardants) was tested. Among them, the auxins 2,4-D, dicamba, and picloram formed most callus (hard and soft). Callus inductions by chitosan and coconut water are novel results for papaya. Shoots only formed in response to BA and TDZ, but TDZ-induced shoots were fascinated and/or hyperhydric. These results provide novel perspectives for papaya researchers who may have recalcitrant genotypes or tissues that are unresponsive in vitro.