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41.
不同继代培养次数对苹果八棱海棠离体培养和遗传转化的影响 总被引:3,自引:0,他引:3
以苹果八棱海棠离体新梢和幼叶为外植体,研究不同继代次数对其离体繁殖、再生和遗传转化的影响。结果表明,随着继代培养次数的增加,继代10次和48次的八棱海棠离体增殖倍数、生根能力、不定芽的再生频率、每外植体再生芽数和GUS基因瞬时表达率均显著高于继代5次的;继代10次的增殖倍数和GUS阳性率明显多于继代48次的,其它指标相互间差异不显著;说明继代10次的芽苗较适合用于八棱海棠离体培养的外殖体材料,其幼叶较适于遗传转化研究。 相似文献
42.
Nothofagus leoni has a restricted distribution in Chilean forests. This work determines suitable culture conditions forin vitro multiplication and rooting through shoots obtained from seedlings. Broadleaved Tree Medium was suitable for shoot multiplication.
A medium with a pulse of 0.55 μM BA in the first subculture and two subcultures on BA-free medium resulted in a multiplication
rate at day 63 of × 5.7, without callus growth or shoot neoformation. Rooted shoots of good quality (number and length of
roots without callus growth) were obtained with 1.23 μM IBA (91.4% of rooting). The first roots appeared at day 11, reaching
a higher speed of rooting at day 15. 相似文献
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A rapid multiplication system for ‘Candidatus Liberibacter asiaticus’ through regeneration of axillary buds in vitro
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LEI Tian-gang HE Yong-rui ZOU Xiu-ping WANG Xue-feng FU Shi-min PENG Ai-hong XU Lan-zhen YAO Li-xiao CHEN Shan-chun ZHOU Chang-yong 《农业科学学报》2022,21(6):1683-1693
‘Candidatus Liberibacter asiaticus (CLas)’, which causes citrus Huanglongbing (HLB) disease, has not been successfully cultured in vitro to date. Here, a rapid multiplication system for CLas was established through in vitro regeneration of axillary buds from CLas-infected ‘Changyecheng’ sweet orange (Citrus sinensis Osbeck). Stem segments with a single axillary bud were cultured in vitro to allow CLas to multiply in the regenerating axillary buds. A high CLas titer was detected in the regenerated shoots on an optimized medium at 30 days after germination (DAG). This titer was 28.2-fold higher than in the midribs from CLas-infected trees growing in the greenhouse. To minimize contamination during in vitro regeneration, CLas-infected axillary buds were micrografted onto seedlings of ‘Changyecheng’ sweet orange and cultured in a liquid medium. In this culture, the titers of CLas in regenerated shoots rapidly increased from 7.5×104 to 1.4×108 cells μg–1 of citrus DNA during the first 40 DAG. The percentages of shoots with >1×108 CLas cells μg–1 DNA were 30 and 40% at 30 and 40 DAG, respectively. Direct tissue blot immunoassay (DTBIA) indicated that the distribution of CLas was much more uniform in regenerated plantlets than in CLas-infected trees growing in the greenhouse. The disease symptoms in the plantlets were die-back, stunted growth, leaf necrosis/yellowing, and defoliation. The death rate of the plantlets was 82.0% at 60 DAG. Our results show that CLas can effectively multiply in citrus plantlests in vitro. This method will be useful for studying plant-HLB interactions and for rapid screening of therapeutic compounds against CLas in citrus. 相似文献
45.
对百合鳞片进行了试管快速繁殖研究.结果表明:外植体取样部位影响百合小鳞茎的增殖率,幼嫩的基部增殖率高,而外部、顶部细胞老化的鳞片增殖率低.百合小鳞茎的形成主要靠不定芽的形成. 相似文献
46.
利用盐场原有设施进行青蛤增养殖技术研究,并对青蛤生长,幼苗放养季节,规格,密度等做了系统研究。增殖试验在一号水库内进行,分两个试验区,382.6公顷为资源繁殖保护区;84.1公顷为移苗增殖区,经过二年多实施,资源繁殖保护区资源量将增9.1倍,净增959.3吨;移苗增殖区资源量净增8.7倍,净增资源量270.7吨,总效益732万元。 相似文献
47.
Summary The EVIKA Research Centre has developed a disease eradication system for the initial material of seed potato, which consists
of 1. Selection of the initial material for eradication, plant thermotherapy, meristem tip cultivation and testing for viruses;
2. Re-eradication (thermotherapy of test-tube plants, cultivation of meristem tips, testing for viruses, testing of varietal
quality and yield of disease-free meristem clones, and the selection of meristem clones with best varietal characteristics;
3. Renewing of the initial material (all processes as above, but the initial material is selected from the seed potatoes grown
for at least 3 years in the field).
Field trials were conducted after the second cycle of eradiaction to determine whether the plantlets were true-to-type and
to assess the yield, disease resistance and tuber dry matter. Recently we have also started in vitro testing of meristem plants
resistance to late blight, hoping that this approach will improve the selection efficiency.
Propagation and growing of the seed tubers consists of 3 main steps: 1. Plantlet propagation in vitro; 2. Greenhouse propagation
in plastic rolls; and 3. Planting the first generation tubers in the field. Under our conditions it is the cheapest, simplest
and most effective way.
Multiplication of the meristem-derived plants is done by shoot tip cuttings in a greenhouse in plastic rolls with peat as
the growing medium. The first generation of seed tubers is grown in the field. In our trials plant productivity was affected
by the method of multiplication, growing conditions and genotype. The highest yield per hectare was obtained with plants multiplied
in plastic rolls. The in vitro plants had more tubers per plant than plants multiplied in plastic rolls. In seed production
fields the productivity of plants was more influenced by following our instructions than by multiplication and growing methods.
The number of tubers per plant obtained with over 0.5 million plants was 6.5–9.0.
In the second generation of seed tubers, grown under equal density, the greater-sized tubers gave more tubers with lower weight
than the smaller-sized tubers. Cutting tubers had no effect on the plant development and tuberization. 相似文献
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A. Giné M. López‐Gómez M. D. Vela C. Ornat M. Talavera S. Verdejo‐Lucas F. J. Sorribas 《Plant pathology》2014,63(6):1446-1453
Several studies were carried out to determine (i) thermal requirements for development, egg production and emergence of juveniles, and completion of the life cycle of Meloidogyne incognita and Meloidogyne javanica on cucumber, (ii) the maximum multiplication rate and the equilibrium density of root‐knot nematodes on cucumber and yield losses in pot and plastic greenhouse experiments, and (iii) the relationships between relative leaf chlorophyll content (RLCC) and relative cucumber dry top weight biomass (RDTWB) in relation to increasing nematode densities at planting (Pi) in pot experiments. Thermal requirements of M. incognita and M. javanica on cucumber did not differ, irrespective of the biological stage. In the pot experiments, M. javanica completed one generation. The maximum multiplication rate (a) was 833, and the equilibrium density (E) varied according to the effective inoculum densities. The relationship between RDTWB and Pi fitted the Seinhorst damage function model. The RLCC value at 40 or 50 days post‐inoculation also fitted the damage model and was related to RDTWB. In greenhouse experiments, conducted from 2009 to 2012, M. incognita completed three generations. The values for a and E were 1147 and 625 second stage juveniles (J2) per 250 cm3 soil, respectively. The tolerance limit was below zero, and the minimum relative yield ranged from 0·12 to 0·34. 相似文献