Cryopreservation of in vitro sugar beet ( Beta vulgaris L.) shoot tips by a vitrification technique

2000 ◽  
Vol 19 (11) ◽  
pp. 1064-1068 ◽  
Author(s):  
B. Vandenbussche ◽  
G. Weyens ◽  
M. De Proft
Keyword(s):  
2013 ◽  
Vol 12 (4) ◽  
pp. 168-178 ◽  
Author(s):  
Farhad Taghipour ◽  
Narges Janalizade ◽  
Maryam Eshrati ◽  
Taraneh Hassanzade ◽  
Fahrul Huyop

Bioenergy ◽  
2021 ◽  
Author(s):  
M. V. Roik ◽  
N. S. Kovalchuk ◽  
O. A. Zinchenko ◽  
L. H. Fedoroshchak ◽  
V. I. Vlasiuk ◽  
...  

Purpose. Investigation of cytogenetic aspects of embryological processes in the culture of immature apomictic embryos, breeding genotypes of sugar beet with cytoplasmic sterility for differentiation and selection by gametophyte reduced parthenogenesis. Methods. Cytological, biotechnological, fluorescent cytophotometry, field, laboratory. Results. The cytogenetic features of genesis of immature apomictic embryos cells induced in vitro on the 12th, 20th and 22th days of development have been investigated on the basis of CMS apozygotic lines of Beta vulgaris and alloplasmic lines of wild species Beta maritime and Beta patula. Indicators of efficiency of haploid reduced parthenogenesis in vitro in alloplasmic lines significantly exceeded the best technologies in pollen-sterile lines of sugar beet from 3.79% to 6.25% and had a value of 62.2%, 24.8%, and 16.7%, respectively. Stabilization of genome ploidy to diploid was carried out in selected breeding numbers without colchicine, based on evaluation and selection of genome ploidy using software of ploidy analyzer (AP) Partec. Conclusions. The efficiency of haploid reduced parthenogenesis induction in vitro in apozygotic CMS breeding genotypes of sugar beet as affected by genetic potential of cytoplasm and taking into account the total percentage of haploids (50 units; 100 units) and myxoploids (50 units; 100 units) has been investigated. Homozygous lines were created by stabilizing the genome ploidy of haploid and myxoploid micro sprouts during III–IV passages without the use of colchicine. Technologies of rooting in the open ground for use in the breeding process of sugar beets have been improved.


2021 ◽  
Vol 31 (1) ◽  
Author(s):  
Nasr A. Ghazy ◽  
Omnia A. Abd El-Hafez ◽  
A. M. El-Bakery ◽  
Dalia I. H. El-Geddawy

Abstract Background Soft rot disease caused by Pectobacterium carotovorum was observed in various crops which lead to yield shortages and economic losses. Main body Therefore, both in vitro and in vivo experiments, aim to assess the effect of nanoparticles and biological treatments to control soft rot disease in sugar beet plant. The treatments comprised three silver nanoparticles (Ag NPs) concentrations (50, 75, and 100 ppm), three Spirulina platensis extract concentrations (50, 75, and 100%), and Bacillus subtilis (1 × 109 CFU ml) 100%. Under in vitro condation, results of the antibacterial activity showed that the zones of inhibition recorded 4.33 cm for 100 ppm Ag NPs, 0.43 cm for 100% algal extract, and 0.2 cm for bacterial treatments. Also, disease incidence % of bacterial soft rot was significantly decreased in all treatments in pot and field experiments. For resistant enzymes activity, B. subtilis 100% showed the most effect (84 mg min−1), followed by S. platensis extract 75%, (57 mg min−1), and Ag NPs 75 ppm (44 mg min−1), for poly phenol oxidase (PPO) at 81 days after sowing (DAS), but at 102 DAS revealed opposite results. On the contrary, peroxidase (PO) at 81 DAS showed different effects where treatment with S. platensis extract 100% increased it significantly (0.546 mg min−1) compared to control (0.535 mg min−1). The same trend was observed at 102 DAS. These results were reflected on sugar quality where Ag NPs 100 ppm treatment recorded the highest significant value (20.5%) followed by S. platensis 75% (19 %); however, the differences among them were not statistically significant. Conclusion This study indicated that the potential benefits of using silver nanoparticles and two biological treatments to control soft rot disease in sugar beet (Beta vulgaris L).


Sugar Tech ◽  
2021 ◽  
Author(s):  
Magdalena Tomaszewska-Sowa ◽  
Anna J. Keutgen

AbstractSugar beet (Beta vulgaris L.) is referred to as a strategic species due to its exceptional economic and functional importance. Sugar beet is cultivated in order to provide material for sugar production as it is the world’s second source after sugar cane. However, in this species, the regeneration of haploid shoots is difficult in comparison to other cultures or isolated microspores. Haploid plants of sugar beet can be derived from in vitro culture mostly via gynogenesis. Therefore, the aim of this research has been to increase the effectiveness of shoot formation from unpollinated sugar beet ovules by optimising the regeneration technique via induced gynogenesis. Various types and concentrations of chosen carbohydrates in media were evaluated. The Murashige and Skoog medium containing 4.4 μmol/L of 6-benzylaminopurine was solidified by 0.7% of agar and enriched with either sucrose (0.06 mol/L or 0.09 mol/L), glucose (0.09 mol/L), fructose (0.09 mol/L), maltose (0.09 mol/L) or with a combination of sucrose (0.04 mol/L) and mannitol (0.04 mol/L) or with sucrose (0.04 mol/L) and fructose (0.04 mol/L). The control medium contained 0.09 mol/L sucrose without any cytokinins. Of all the analysed media, the best for shoot regeneration turned out to be the media with 4.4 µmol/L 6-benzylaminopurine, solidified with 0.7% agar, additionally containing 0.09 mol/L glucose or 0.06 mol/L sucrose. On those media, over three-fold more shoots compared with the control medium were produced.


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