Search results for "Tissue culture"

In vitro control of adventitious bud differentiation by inorganic media components in leaves of matureJuniperus oxycedrus

1995

The effects of changes in the concentration of macronutrients on BA-induced caulogenesis from leaves of matureJuniperus oxycedrus cultured on modified Murashige and Skoog or Schenk and Hildebrandt media are reported. The bud-forming capacity of the explants depended mainly on the ratios among the levels of ammonium, nitrate, and potassium. The most favorable media formulations for differentiation of adventitious buds were those with nitrate:potassium, ammonium:potassium, and nitrate:ammonium ratios near 1, around 0.1, and between 9 and 15, respectively. The total ionic strength of the media limited bud induction, but only when a disequilibrium of these ratios was produced.

Selection and long-term cultures of high-yielding Digitalis obscura plants: RAPD markers for analysis of genetic stability

1996

Fifteen wild-growing plants of Digitalis obscura collected in three differents regions were characterized according to their capacities to biosynthesize cardenolides and to proliferate in vitro. Great genotype-dependent variabilities were found in both parameters. Selected genotypes were differentiated using randomly amplified polymorphic DNA (RAPD) markers. Once an elite genotype with high-yielding properties was isolated and micropropagated during 2 years, identity of the donor plant and the regenerants was confirmed by RAPD analysis.

�ber den Nachweis des Erythropoetins in der Gewebekultur

1958

GAMETIC AND SOMATIC EMBRYOGENESIS BY ANTHER CULTURE TECHNIQUE IN CITRUS AND IN OTHER MEDITERRANEAN FRUIT TREES

2010

Rates of uptake and metabolism of indole-3-acetic acid and 2,4-dichlorophenoxyacetic acid by cultured leaf segments at different stages of developmen…

1987

Immature leaf tissue of Triticum timopheevi Zukh. responded to supplied auxin and showed cell division in culture. The rates of uptake and of metabolism of indole-3-acetic acid and 2,4-dichlorophenoxyacetic acid by such tissues were measured and compared with those of mature auxin-unresponsive tissue. The purpose of these experiments was to determine whether or not the concentration of auxin in cultured mature tissue was a factor limiting the cell division response to auxin. The data indicate that neither alterations in rates of uptake nor alterations in rates of metabolism could explain the loss of responsiveness to auxin which apparently occurs during cell differentiation. The results are…

The ambiguous role of 2,4-dichlorophenoxyacetic acid in wheat tissue culture

1986

The very basal, highly immature regions of dissected young leaves of Triticum aestivum L. cv. Kite formed adventitious roots on a nutrient medium supplemented with comparatively low concentrations (0.16 to 0.63 μM) of 2,4-dichlorophenoxyacetic acid (2,4-D). Higher concentrations (up to 640 μM) had to be applied to stimulate growth from more mature regions higher up the leaf. Yet, already at 2.5 μM roots were less distinct and more callus-like, and eventually (at 10 to 640 μM) only a subculturable callus of apparently suppressed, slowly proliferating root primordia developed. Furthermore, at the most basal, highly immature regions growth was significantly retarded when the auxin concentratio…

Factors influencing axillary shoot proliferation and adventitious budding in cedar.

2005

We developed procedures for in vitro cloning of Cedrus atlantica Manetti and C. libani A. Rich explants from juvenile and mature plants. Explant size was one determinant of the frequency of axillary bud break in both species. Shoot tips and nodal explants mainly developed calli, whereas bud sprouting occurred in defoliated microcuttings cultured on a modified Murashige and Skoog medium without growth regulators. Isolation and continuous subculture of sprouted buds on the same medium allowed cloning of microcuttings from C. atlantica and C. libani seedlings and bicentennial C. libani trees, thus providing a desirable alternative for multiplying mature trees that have demonstrated superior ch…

Effect of auxin on the mitotic cell cycle in cultured leaf segments at different stages of development in wheat

1987

Young leaves of Triticum timopheevi Zukh. show a defined gradient of development. One-mm-long sections from such leaves were cultured in vitro. At a low concentration of exogenous auxin, cells in the most basal, highly meristematic explants divided readily in culture, but in the absence of auxin they soon ceased dividing and were arrested in G1 and G2 of the mitotic cell cycle. In the region adjoining the meristem, where most cells were arrested in G1, very high concentrations of auxin had to be applied to reinitiate cell division, i.e. stimulate transitions from G1 to S-phase and from G2 to mitosis. Above this potentially auxin-responsive region, which represented less than 50% of the tota…

Moss cell cultures as sources of arachidonic and eicosapentaenoic acids

1986

AbstractLipid classes from tissue cultures of the moss Leptobryum pyriforme (Hedw.) Wils. were analyzed. In the total lipid fraction, this species contained 20% arachidonic acid and about 7% eicosapentaenoic acid. The distribution of these fatty acids showed a preference for the phospholipid fraction. In particular, the phosphatidylethanolamine fraction was enriched in arachidonic acid. The arachidonic acid content of Leptobryum could be altered by transferring the cultures to different culture conditions. Mosses show high organic mass production in tissue cultures in relatively simple media. The great potential of using mosses as sources for the production of polyunsaturated fatty acids is…

Effect of plant growth regulators and basal media onin vitro shoot proliferation and rooting ofMyrtus communis L.

1996

The influence of macronutrients and growth regulators on in vitro shoot proliferation and rooting of an East Spanish population ofMyrtus communis L. were studied. Preincubation of field material on a medium without mineral salts prevented the browning from phenolic exudates. For multiplication, nodal segments of 5 mm fromin vitro produced shoots were cultured on Murashige and Skoog (MS), Schenk and Hildebrandt (SH) and Heller (H) media (full strength or diluted to 1/2 or 1/4), with 6-benzylaminopurine (BAP) at concentrations 4.4, 13.3 and 22.2 ΜM or kinetin (K) at concentrations 4.7, 14.0 and 23.2 ΜM. The optimum shoot proliferation was on quarter-strength MS medium with 4.4 ΜM BAP, whereas…