4 research outputs found
Recent advances in flower color alteration by metabolic manipulation of carotenoid biosynthesis
U hortikulturi je prisutna stalna potreba za ukrasnim biljkama sa novim karakteristikama, gde boja
cveta predstavlja jednu od najvažnijih osobina koja određuje njihovu komercijalnu vrednost. Sa razvojem
metoda genetičkog inženjeringa otvorena je mogućnost kreiranja biljaka sa željenom bojom cvetova koja
se ne može postići klasičnim ukrštanjem ili mutagenezom. Boja cvetova kod biljaka određena je sadržajem
tri biljna pigmenta: antocijanina, karotenoida i betalaina. Do sada, najveći napredak postignut je genetičkom
modulacijom biosinteze antocijanina. Na ovaj način postignute su nove boje cvetova kod
najmanje 50 ukrasnih vrsta, a neki od tih modifikovanih varijeteta su već dugi niz godina u slobodnoj prodaji.
Međutim, promena boje cveta manipulacijom biosintetskog puta karotenoida je dokumentovana
kod svega nekoliko ukrasnih vrsta i poslednjih godina intenzivirana su istraživanja u tom pravcu. U ovom
radu je razmatran potencijal ovog pristupa, sa posebnim osvrtom na rezultate postignute na promeni boje
cvetova kod kultivara ljubičice uvodjenjem gena za kapsantin-kapsorubin sintazu.In horticulture, there is a constant need for ornamental plants with new characteristics, where the flower
color is one of the most important features that determines their commercial value. With the development
of genetic engineering methods, it has been possible to create plants with the desired flower
color which cannot be achieved by classical breeding or mutagenesis. The flower color in plants is determined
by the content of three plant pigments: anthocyanins, carotenoids and betalains. Up to date, the
greatest progress has been made by genetic modulation of anthocyanin biosynthesis. In this way, the new
flower colors have been achieved in at least 50 ornamental species, and some of these modified varieties
have been on market for many years. However, the alteration of flower color by manipulating the carotenoid
biosynthetic pathway has been documented in only a few ornamental species, and the research has
been significantly increased last few years. In this paper, the potential of this approach is considered, with
special reference to the results achieved on flower color alteration of pansy cultivars by introducing the
gene for capsanthin-capsorubin synthase
Elimination of TSWV from Impatiens hawkerii Bull. and regeneration of virus-free plant
The possibility for obtaining virus free plants from Impatiens hawkerii Bull. shoots infected with Tomato spotted wilt virus (TSWV) through meristem-tip culture was examined. TSWV presence in I. hawkerii plants was detected by DAS-ELISA and RT-PCR and identification of the virus was confirmed by sequencing one of the chosen isolate (GenBank Accesion CQ132190). Meristem-tip explants (0.3-1.5 mm) from virus-infected shoots are cultured on MS media supplemented with different concentrations of the cytokinins, CPPU or TDZ (0.01-1.0 mu M), respectively. Using this system, a large number of in vitro shoots could be produced from a single explant. Also, cytokinins showed a stimulatory effect on the length, fresh and dry weights of the newly formed shoots. Plant pigments content in I. hawkerii shoots increased significantly in the presence of cytokinins. Rooting of shoots was spontaneous on the same media. Rooted plantlets were transferred to soil where 97% successfully acclimatized. By DAS-ELISA and RT-PCR, 80% of the in vitro plantlets were shown to be a virus-free. Considering these, the present protocol seems to be an efficient method for in vitro generation of virus-free I. hawkerii plantlets by meristem tip cultures
Primena tehnika in vitro kulture za eliminaciju virusa iz ukrasnih biljaka
Viruses are responsible for numerous epidemics in different crops in all parts of the world. As a consequence of their presence great economic losses are being incurred. In addition to the development of sensitive techniques for detection, identification and characterization of viruses, substantial attention has also been paid to biotechnological methods for their elimination from plants. In this review article, the following biotechnological in vitro culture techniques for virus elimination from ornamental plants are presented: meristem culture, thermotherapy, chemotherapy, cryotherapy or a combination of these methods. The plant species, as well as the type of virus determine the choice of a most suitable method. The state of the art in investigation of virus elimination from Impatiens sp. in Serbia is summarized.Virusi su odgovorni za brojne epidemije na različitim usevima u svim delovima sveta. Posledica njihovog prisustva su velike ekonomske štete, pa osim razvoju osetljivih tehnika za detekciju, identifikaciju i karakterizaciju virusa, velika pažnja se poklanja i biotehnološkim metodama za njihovu eliminaciju. U ovom preglednom radu predstavljene su tehnike in vitro kulture za eliminaciju virusa iz biljnog materijala: kultura meristema, termoterapija, hemoterapija, krioterapija ili kombinacija ovih metoda. Koja će metoda biti primenjena zavisi od biljne vrste, kao i od vrste virusa. U radu je dat pregled istraživanja na eliminaciji virusa iz Impatiens sp. u Srbiji
Elimination of TSWV from Impatiens hawkerii Bull. and regeneration of virus-free plant
The possibility for obtaining virus free plants from Impatiens hawkerii
Bull. shoots infected with Tomato spotted wilt virus (TSWV) through
meristem-tip culture was examined. TSWV presence in I. hawkerii plants
was detected by DAS-ELISA and RT-PCR and identification of the virus
was confirmed by sequencing one of the chosen isolate (GenBank Accesion
CQ132190). Meristem-tip explants (0.3-1.5 mm) from virus-infected
shoots are cultured on MS media supplemented with different
concentrations of the cytokinins, CPPU or TDZ (0.01-1.0 µM),
respectively. Using this system, a large number of in vitro shoots
could be produced from a single explant. Also, cytokinins showed a
stimulatory effect on the length, fresh and dry weights of the newly
formed shoots. Plant pigments content in I. hawkerii shoots increased
significantly in the presence of cytokinins. Rooting of shoots was
spontaneous on the same media. Rooted plantlets were transferred to
soil where 97% successfully acclimatized. By DAS-ELISA and RT-PCR, 80%
of the in vitro plantlets were shown to be a virus-free. Considering
these, the present protocol seems to be an efficient method for in
vitro generation of virus-free I. hawkerii plantlets by meristem tip
cultures