Recovery of fertile plants from isolated,cultured maize shoot apices

Maize shoot apices (1 to 2mm size) from two sources were used to recover normal plantlets. The first explant source included shoot apices from the embryonic axis of immature embryos, 12–14 days post pollination in the glasshouse (spring) or 15–20 days post pollination in the summer nursery. In most explants, the shoot apical meristem was surrounded by a coleoptile primordium which was removed before culture. The second explant source included shoot apices from the plumules of 72 h imbibed mature kernels. The coleoptile and all other leaf layers (leaf-1 to leaf-3 or 4) of the plumule were removed before culture to expose the apical meristem. Among the genotypes studied, a recovery of 43% (Mo17) to 100% (Oh43) of plantlets was achieved from shoot apices from immature embryo plumules cultured in MS medium. Recovery of 80% of Oh43 plantlets in MS medium and 40% of A188 plantlets from apices of plumules of imbibed (72 h) seeds in MS medium containing 2,4-dichlorophenoxyacetic acid was recorded. The plantlets derived from both explant sources grew normally and produced viable seeds upon pollination.     

罗汉果不同器官直接分化再生苗的研究

以青皮果品种的叶片、叶柄和无芽茎段作为外植体,研究其直接分化再生苗能力的差异。结果表明:⑴MS 6-BA1.0mg/L IAA0.1mg/L和MS 6-BA2.0mg/L IAA0.1mg/L两组培养基均可使叶片外植体直接分化出芽并建成再生苗。叶片基部的分化能力最强,中部稍次,尖部最弱。⑵MS 6-BA3.0mg/L IAA0.1mg/L则诱导叶片外植体首先脱分化形成愈伤组织,继而再分化成再生苗,,且畸形苗居多,无应用价值。⑶叶柄和无芽茎段在三组培养基中都只能脱分化形成大量愈伤组织,难以分化再生苗。     

Direct Organogenesis in Hypocotyl Cultures of Tamarindus Indica

Direct differentiation of shoot buds from hypocotyl segments of 12-d-old seedlings of Tamarindus indica was obtained on Murashige and Skoog (MS) medium with or without growth regulators. The highest regeneration (66 %) and the maximum number of shoots (3 - 4) per explant were obtained from the explants on MS medium containing 6-benzylaminopurine (5 × 10-6 M). A maximum roots per shoot were produced on medium containing 3-indole butyric acid (5 × 10-6 M). The resulting plantlets were hardened and transferred to soil in pots where 75 % of them survived and resumed growth. Histological examination of explants suggests that the shoots were of de novo origin which would make this system suitable for transformation experiments. This revised version was published online in July 2006 with corrections to the Cover Date.     

Regeneration of niger (Guizotia abyssinica Cass.) CV Sahyadri from seedling explants

Root, hypocotyl and cotyledonary explants of niger (Guizotia abyssinica Cass) CV. Sahyadri were aseptically cultured on Murashige and Skoog's basal medium (MS) containing BAP and kinetin. Multiple shoot regeneration was induced from hypocotyl and cotyledonary explants while root explants produced only callus on MS medium supplemented with BAP. BAP (1 mg l^-1) was optimum for shoot regeneration. Regenerated shoots were transferred to MS medium without auxins, with auxins and with increasing concentrations of sucrose for rooting. Complete plantlets were obtained in all cases; however, 0.5 mg l^-1 NAA was the best for induction of roots. Ninety-seven per cent of the plantlets survived and completed their life cycle when transferred to natural conditions.Abbreviations BAP 6-benzylamino purine - NAA -naphthaleneacetic acid - IAA indole-3-acetic acid - IBA indole-3-butyric acid     

Regeneration in cultures of Papaver bracteatum as influenced by growth hormones and temperature

Callus was induced on Papaver bracteatum Lindl. seedlings inoculated on Murashige & Skoog (1962) medium supplemented with -naphthaleneacetic acid (NAA) (1.0 mg 1^-1) and benzylamine purine (BA) (0.5 mg 1^-1). Subculture resulted in excellent callus proliferation but no organogenesis. Shoots were regenerated in cultures grown on MS medium containing NAA (1.0 mg 1^–1), BA (0.5 mg 1^–1) and casein hyrdrolyzate (2.0 mg 1^-1). The shoots developed into plantlets after 8 weeks of culture, and were induced to root on 1/2 MS without the addition of growth regulators. The rooted plantlets were transferred to soil after hardening.MS at full strength was found inhibitory for callus induction and proliferation, but 1/2 MS was suitable. Similarly callus growth was very slow at 25°C but increased when the temperature was lowered to 15°C as did bud initiation.Abbreviations BA benzylamine purine - IAA indoleacetic acid - K kinetin (6-furfurylamino purine) - NAA -naphthalene acetic acid - 2,4-d 2,4-dichlorophenoxyacetic acid     

Plate-shaped nuclear pole bodies in the monothalamous foraminiferKibisidytes sp.

Summary Cultures capable of continuous plantlet production have been established from excised, immature embryos ofSorghum bicolor and the course of development of the plantlets has been followed by light and scanning electron microscopy. Such analyzes revealed that there are two distinct methods of plantlet production. Shoot primordia and embryo-like structures arisede novo from cells of the scutellum. However, when these cultures are transferred to fresh medium a further proliferation of shoot buds occurs by the formation of axillary shoot primordia. The cultures are therefore more comparable to shoot cultures than to callus cultures. Over 300 plantlets producedin vitro have been transferred to potting compost and grown to maturity. Most plants flowered and set seed. Fifteen plants were sterile but were of normal chromosome number (2 n=20) and it is presumed that the sterility was due to segregation of restorer genes in the immature embryos used to initiate some of the cultures.Abbreviations used in the text 2,4-D 2,4 dichlorophenoxyacetic acid - MS Murashige and Skoog - NAA -Naphthalene acetic acid - 6-BAP 6-Benzylaminopurine     

In vitro propagation of Typhonium flagelliforme (Lodd) blume

Summary An in vitro culture system was developed for Typhonium flagelliforme using buds from the rhizomes. The mineral salts of four media were tested. These were Murashige and Skoog (MS), Nitsch and Nitsch (NN), Gamborg B5 (GB5) and White (W) of which MS medium was found to be the best medium for in vitro culture of T. flagelliforme. The addition of as low as 0.1 mg l⁻¹ (0.54 μM) α-naphthalene acetic acid (NAA) with the presence or absence of N⁶-benzyladenine (BA) in the MS medium caused abnormal shoot formation. The best medium for maximizing shoot number combined with normal complete plantlets from each bud was MS medium supplemented with 0.3 mg l⁻¹ (1.33 μM) BA and 0.5 mg l⁻¹ (2.46 μM) indole-3-butyric acid (IBA). The best acclimatization process was to transfer the normal plantlets, with all the leaves removed, into sand plus coconut husks substrate (1∶1) and placed in intermittent water mists house or shaded plant house with 50% light exclusion. Ninety two percent of the plantlets survived using this acclimatization method.     

Potential implications of biopriming in banana (Musa spp) plantlets against banana bunchy top virus (BBTV)

Abstract

Transplant media as a means for the introduction of biological agents is currently being investigated in a variety of crops. This study aimed to investigate the impact of microbial inoculation in micropropagated banana plantlets to enhance their resistance against Banana bunchy top virus (BBTV). Virus indexed micropropagated plantlets of banana were subjected to root colonization followed by foliar spraying with bacterial strains Pseudomonas fluorescens Pf1, CHA0 and Bacillus subtilis EPB22 during primary and secondary hardening stage in the nursery, at the time of repotting and 3 months after planting in the pot. Microbe inoculated plantlets showed enhanced PR proteins and defense enzymes besides reducing banana bunchy top disease incidence under glasshouse condition. The results indicated the effective use of beneficial microbes in reducing the disease incidence of BBTV in tissue culture banana plantlets. In addition, the molecular characterization of endophytes isolated from banana plantlets, using SDS-PAGE and RAPD-PCR revealed that endophytes were categorized into two distinct groups. These results emphasize the significance of microorganisms in protection of young plantlets from transplanting stresses in field. Further, the use of beneficial microorganisms instead of chemicals sustains an ecological niche in the agricultural ecosystem.     

Effects of several establishment modes of Miscanthus × giganteus and Miscanthus sinensis on yields and yield trends

Miscanthus is a C4 perennial grass originating from East Asia, the yields of which progressively increase in the first years of growth. Several species for bioenergy have been studied since the mid‐1980s in Europe, in particular (Miscanthus × giganteus [M. × giganteus]), due to its high yields. M. × giganteus is mainly cultivated in France and established from rhizomes. Our study aimed to assess, in field conditions, alternative establishment methods combined with an alternative species, Miscanthus sinensis (M. sinensis). We set up a multi‐environment experimental network. On each trial, we tested two treatments with M. × giganteus, established from rhizomes (G_r‐sd) and from plantlets obtained from rhizomes (G_p‐sd), and two treatments with M. sinensis seedlings transplanted in single (S_p‐sd) and double density (S_p‐dd). ANOVA was performed to compare establishment and regrowth rates across treatments, as well as yields across treatments and site‐years. A logistic model was used to describe yield trends and to compare the maximum yield reached and the rate of yield increase of both species. Results showed that miscanthus establishment from plantlets resulted in higher establishment (between 87% and 92%) and regrowth (between 91% and 94%) rates compared to establishment from rhizomes. Treatments with M. × giganteus obtained higher average yields across site‐years than those with M. sinensis, but more variable yields across site‐years. We showed a strong species effect on yields, yield components (shoot weight, shoot density and shoot number per plant) and light interception (through leaf area index). Lastly, to use M. sinensis established from transplanted plantlets as an alternative to M. × giganteus, research would be required on the breeding of M. sinensis sterile seeds to avoid risks of invasiveness.     

黄独脱毒苗快繁及产业化技术探讨

以黄独脱毒苗为试材,采用植物组织培养方法研究不同因素对脱毒苗快繁技术的影响。结果表明,在黄独脱毒苗快繁中,白砂糖可替代蔗糖,果酱瓶可替代三角瓶,液体培养优于固体培养,但自来水不能代替蒸馏水。黄独脱毒苗在移栽的过程中,气孔关闭率在第5天时达到最高,以后气孔逐渐恢复关闭功能。脱毒苗与非脱毒苗的块茎在直径和鲜重上均有显著差异,表明黄独经脱毒后可提高产量。