Previous Page  4 / 21 Next Page
Information
Show Menu
Previous Page 4 / 21 Next Page
Page Background

Page 46

conferenceseries

.com

Volume 8

Journal of Biotechnology & Biomaterials

ISSN: 2155-952X

Biotech Congress 2018 & Enzymology 2018

March 05-07, 2018

JOINT EVENT

20

th

Global Congress on

Biotechnology

3

rd

International Conference on

Enzymology and Molecular Biology

&

March 05-07, 2018 London, UK

Notes:

Development of approach to obtain

Brachypodium distachyon

L. regenerative plants with morphogenetic

stability

Omirbekova N Zh, Mursalieva V K, Zhusupova A I, Zhunusbaeva Zh K

and

Kenzhebaeva S S

Al-Farabi Kazakh National University, Kazakhstan

T

he aim of the research is development of effective methodological approaches of

in vitro

cultivation, object 21 line (BD21) B.

distachyon. In order to develop cultivation methods, ability for callus formation, regeneration of generative and vegetative organs

of VD21 was studied. To cultivate, Linsmayer-Skoog and Murashige-Skoog medium, additional introduction of phytohormones

was used. Aseptic culture conditions for callusogenesis cultivation: under dark conditions at a temperature of 24°C, for t shoots

regeneration: 16/8 hour photoperiod and lighting of 3000 lux. Inflorescence and immature embryos isolated from green spikes of

vegetating plants and isolated embryos from mature seeds were used as primary explants to induce callus formation

in vitro

. During

immature embryo cultivation, callus formation takes place near the corimbe for 20-25 days. During the cultivation of whole caryopsis

with mature embryos, the sprouts grew after a week of cultivation on MS medium without hormones. The level of maturity of isolated

caryopsis has a significant influence on the callus formation and the type of callus tissue. The mature caryopsis formed callus on

the 10th day of cultivation with a frequency of 75%. The cultivation of the overgrown caryopsis in the dark on medium MS 1 with

2 mg/L 2.4 DPA, led to the formation of a primary shoot in 60% of explants; the formation of callus in the area of the scute, but for

30-35 days. Passage of the callus on the same medium and on the hormone-free medium led to the appearance of greenish pointwise

impregnation of 30% of the calluses. For microclonal propagation, nodal segments of young shoots of plants were introduced into the

culture. To culture introduction, side shoots 5 cm long with 3-4 interstitial sites were cut, the microcrops were planted in inducing

media. The shoot-forming capacity of primary explants was about 59%; the multiplication factor for two passages was 5.7.

Recent Publications

1.

Omirbekova N, Kenzhebayeva S, Capstaff N, Fatma Sarsu, et al. (2017) Searching a spring wheat mutation resource for

correlations between yield, grain size, and quality parameters. Journal of Crop Improvement 31:209-228.

2.

Omirbekova N, Kenzhebayeva S, Doktyrbay G et al. (2016) Frequency of vernalization requirement associated dominant

VRN-A1 gene and earliness related Esp-A1 candidate genes in advanced wheat mutant lines and effect of allele on flowering

time. International Journal of Biology and Chemistry 9:24-30.

3.

Omirbekova N, Zhussupova A and Zhunusbayeva Zh (2015)

Brachypodium distachyon

as a model plant in wheat rust

research. International Journal of Biology and Chemistry 2:52-55.

Biography

Omirbekova N Zh graduated from Al-Farabi Kazakh National University and Lomonosov Moscow State University and has completed her Doctoral studies from

Al-Farabi Kazakh National University. She is currently a Professor at the Department of Molecular Biology and Genetics, School of Biology and Biotechnology

of KazNU named after Al-Farabi (Republic of Kazakhstan). Her research interests include chemical mutagenesis, genetics and biochemistry of wheat. She has

published more than 30 papers in high valued journals.

nargul.tata@gmail.com

Omirbekova N Zh et al., J Biotechnol Biomater 2018, Volume 8

DOI: 10.4172/2155-952X-C2-091