Kinetics of Douglas-fir (Pseudotsuga menziesii) somatic embryo development

1998 ◽  
Vol 76 (5) ◽  
pp. 863-871 ◽  
Author(s):  
Ryan P Taber ◽  
Chun Zhang ◽  
Wei-Shou Hu

Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco) is one of the most economically important softwood species in the Pacific Northwest region. Somatic embryogenesis is a potential mass propagation technology for increasing the productivity of existing forest acreage. Combined with traditional breeding methods and recent advances of genetic engineering in plant species, somatic embryos can shorten the elite clone selection process significantly. Somatic embryo culture of Douglas-fir involves three stages: maintenance, abscisic acid (ABA) singulation, and maturation. At the beginning of all stages of culture, the population of cells with embryogenic potential is increased through the weekly subcultured maintenance stage; transfer into the ABA singulation stage initiates embryo development, while cotyledonary embryos are formed in the maturation state. The first two stages were carried out in submerged suspension culture, while during the maturation stage the developing embryos were placed on a polyester pad in a Petri dish. The growth kinetics in these stages were investigated. Fresh and dry weights were observed to double in the maintenance stage, while a smaller increase occurred in the ABA singulation stage. NH4+ was consumed preferentially to NO3- in all culture stages. Sucrose, the primary carbon source, was hydrolyzed to glucose and fructose rapidly. During cultivation, glucose and fructose were consumed simultaneously. The hydrolysis of sucrose resulted in a slight osmolarity increase at the beginning of all culture stages, while the subsequent consumption of glucose and fructose coincided with a gradual decrease in osmolarity. This dynamic osmolarity pressure profile is most profound in the maturation stage, in which the initial high osmotic pressure of 600 ± 20 mOsm/kg (mean ± SD) increased to 700 ± 27 mOsm/kg after sucrose was hydrolyzed but decreased to 350 ± 14 mOsm/kg after the depletion of sugars at the end of cultivation. The complete process of embryo development, from the week-long maintenance culture, through the weekly subcultured ABA singulation culture, to the maturation of embryos took between 70 and 80 days. Each millilitre of culture present at the onset of maintenance culture gave rise to approximately 420 mature embryos. During that same time period, the biomass increased approximately 100 times. Prolonging the cultivation time failed to increase the yield of mature embryos. These results give a more complete view of the kinetic behavior of developing Douglas-fir embryos and will aid in the optimization and scale-up of this important process.Key words: somatic embyrogenesis, Douglas-fir, Pseudotsuga menziesii, growth kinetics, ABA, osmolarity, development.

2018 ◽  
Vol 8 ◽  
pp. 1293-1308
Author(s):  
D. K. Isutsa ◽  
R. N. Mayoli ◽  
A. B. Nyende ◽  
C. M. Mweu

Coffee is one of the most important crops cultivated in the world for use in beverages and confectionaries. Embryogenesis is a complex process that begins with a single cell and ends with the formation of mature embryos. Somatic embryo development involves accumulation of complex metabolites and storage reserves. This present experiment identified and quantified endogenous phytocomponents and amino acids present during somatic embryogenesis of ‘Ruiru 11’. Laboratory experiments for this study were set up in the Coffee Research Institute, Kenya at Ruiru. Third leaf pair explants were excised from 8-month-old greenhouse-grown mother plants sterilized and cultured in half strength Murashige and Skoog basal salts augmented with Thidiazuron. Once embryos had developed, the cultures were analysed for phytocomponents using GCMS and HPLC. The results showed that palmitoleic and stearic acids were highest (23.3 µg/g and 69.9 µg/g respectively) in brown embryogenic cultures. Cis 7,8 epoxy-2-methyl octadecane was highest (253 µg/g) in green embryogenic cultures. (Z)-3-Tetradecene was highest (25 µg/g) in brown non-embryogenic cultures. Z, Z-3,13- Octadecedien-1-ol and (Z)-7-Hexadecenal were highest (32.1 µg/g and 70.2 µg/g respectively) in green embryogenic cultures. Alanine content was highest (4.4 µg/g) in embryos of brown cultures. Amino acids, fatty acids and their derivatives are potential biomarkers for embryogenesis. Other phytocomponents should be identified and their role in coffee somatic embryogenesis determined. Further studies regarding the status of the phytocomponents identified in the present study, especially in particular stages of embryo development are needed to propose treatments to improve coffee somatic embryo development.


HortScience ◽  
1994 ◽  
Vol 29 (11) ◽  
pp. 1349-1352 ◽  
Author(s):  
Whei-Lan Teng ◽  
Yann-Jiun Liu ◽  
Yu-Ching Tsai ◽  
Tai-Sen Soong

A bioreactor was used to establish a scale-up system for somatic embryogenesis in `Scarlet' carrot (Daucus carota L.). At a cell density of 1–2 × 106 cells/ml, mature and germinating embryos could be observed within 4 to 5 weeks. As cell density exceeded 2 × 106 cells/ml, the culture turned darker yellow, and embryo development was inhibited. Cell densities below 106 cells/ml resulted in abnormal embryos. Bioreactor design had a critical impact on somatic embryogenesis due to various types and the strength of shear forces generated. In this study, an air-lift bioreactor was selected from three different types (spinner flask, screen column bioreactor, and air lift) because it resulted in the highest biomass production and somatic embryogenesis. Foaming was eliminated by preculture of embryogenic cells in flasks; cells were then sieved on a 60-μm polyester screen and thoroughly rinsed with distilled water before being transferred to the bioreactor. Such preculture for at least 10 days significantly increased the regeneration of somatic embryos. During somatic embryogenesis, dissolved O2 concentrations decreased to 33% of saturation, and then increased up to 80% when embryo development approached maturity and mature embryos germinated. Bioreactor-cultured embryos germinated with relatively short cotyledons and long roots, whereas flask-cultured embryos germinated with relatively long cotyledons and short roots.


Plant Disease ◽  
2013 ◽  
Vol 97 (6) ◽  
pp. 744-748 ◽  
Author(s):  
Jerry E. Weiland ◽  
Bryan R. Beck ◽  
Anne Davis

Pythium species are common soilborne oomycetes that occur in forest nursery soils throughout the United States. Numerous species have been described from nursery soils. However, with the exception of P. aphanidermatum, P. irregulare, P. sylvaticum, and P. ultimum, little is known about the potential for other Pythium species found in nursery soils to cause damping-off of tree seedlings. A greenhouse study was conducted to evaluate the pathogenicity and virulence of 44 Pythium isolates representing 16 species that were originally recovered from soil at three forest nurseries in Washington and Oregon. Seeds of Douglas-fir (Pseudotsuga menziesii) were planted into soil infested with each of the isolates. Seedling survival, the number of surviving seedlings with necrotic root lesions, and taproot length were evaluated 4 weeks later. Responses of Douglas-fir to inoculation varied significantly depending on Pythium species and isolate. Eight species (P. dissotocum, P. irregulare, P. aff. macrosporum, P. mamillatum, P. aff. oopapillum, P. rostratifingens, P. sylvaticum, and P. ultimum var. ultimum) significantly reduced the number of surviving seedlings compared to the noninoculated treatment. However, all Pythium species caused a greater percentage of seedlings to develop root lesions (total mean 40%) than was observed from noninoculated seedlings (17%). Taproot length varied little among Pythium treatments and was not a useful character for evaluating pathogenicity. Results confirm the ability of P. irregulare, P. mamillatum, and P. ultimum var. ultimum to cause damping-off of Douglas-fir seedlings, and are indicative that other species such as P. dissotocum, P. aff. macrosporum, P. aff. oopapillum, P. rostratifingens, and P. sylvaticum may also be responsible for seedling loss.


1998 ◽  
Vol 28 (8) ◽  
pp. 1198-1206 ◽  
Author(s):  
Paige E Axelrood ◽  
William K Chapman ◽  
Keith A Seifert ◽  
David B Trotter ◽  
Gwen Shrimpton

Poor performance of Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco) plantations established in 1987 has occurred in southwestern British Columbia. Affected sites were planted with 1-year-old container stock that exhibited some root dieback in the nursery. A study was initiated in 1991 to assess Cylindrocarpon and Fusarium root infection in planted and naturally regenerating (natural) Douglas-fir seedlings from seven affected plantations. Percentages of seedlings harboring Cylindrocarpon spp.and percent root colonization were significantly greater for planted seedlings compared with natural seedlings. A significant linear trend in Cylindrocarpon root colonization was observed for planted seedlings with colonization levels being highest for roots closest to the remnants of the root plug and decreasing at distances greater than 10cm from that region. This trend in Cylindrocarpon colonization was not observed for natural seedlings. Cylindrocarpon destructans (Zins.) Scholten var. destructans and C.cylindroides Wollenw. var. cylindroides were the only species isolated from planted and natural conifer seedlings. For most sites, percentage of seedlings harboring Fusarium spp.and percent Fusarium root colonization were less than for Cylindrocarpon. Recovery of Fusarium spp.from seedlings and root colonization levels were not significantly different for planted and natural seedlings from all sites.


1989 ◽  
Vol 1 (12) ◽  
pp. 1137-1146 ◽  
Author(s):  
J L Zimmerman ◽  
N Apuya ◽  
K Darwish ◽  
C O'Carroll

2004 ◽  
Vol 161 (2) ◽  
pp. 229-236 ◽  
Author(s):  
Dunja Leljak-Levanić ◽  
Nataša Bauer ◽  
Snježana Mihaljević ◽  
Sibila Jelaska

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