Mecoprop as a growth factor in wheat and rye tissue cultures

1979 ◽  
Vol 57 (14) ◽  
pp. 1479-1483 ◽  
Author(s):  
Estela Sánchez de Jiménez ◽  
Ezequiel Murillo

Wheat and rye calli were induced on Murashige–Skoog medium by the addition of 2, 4-D[(2,4-dichlorophenoxy)acetic acid]. The effect of Mecoprop [2(4-chloro-2-methyl)phenoxy propionic acid], an analogue of this auxin, was also tested and the rates of callus growth were compared with the ones obtained with 2, 4-D. On Murashige–Skoog medium, Mecoprop induced and supported callus growth of the various cereals tested more efficiently than did 2, 4-D. This effect was more pronounced on wheat callus. When both auxins were present in the culture medium, the enhancing effect of Mecoprop was slightly higher. The specific affinity of both auxins for wheat chromatin was measured. The results indicated that both substances, 2, 4-D and Mecoprop, selectively dissolve wheat chromatin. However, lower concentrations of Mecoprop than of 2, 4-D are required to dissolve the same amount of chromatin. It is concluded that in cereal cell cultures, Mecoprop is a more efficient growth factor than 2, 4-D.

1975 ◽  
Vol 53 (10) ◽  
pp. 957-963 ◽  
Author(s):  
D. Dudits ◽  
G. Nemet ◽  
Z. Haydu

Callus cultures of wheat (Triticum aestivum L.) were established by incubation of segments from root tips, shoots of seedlings, and from rachis with B5 and T media. 2,4,5-Tri-chlorophenoxyacetic acid, Benazolin, and Banvel D (Dicamba) were found to be appropriate growth regulators for initiation and maintenance of wheat callus cultures. Cytokinins inhibited callus growth. This effect was less pronounced with zeatin than with kinetin and benzyladenine. Supplementation of media with cytokinins, however, increased the number of roots formed in the callus. Shoots and complete plants were regenerated from rachis and shoot callus.


1985 ◽  
Vol 108 (4) ◽  
pp. 545-549 ◽  
Author(s):  
Mitsuhide Naruse ◽  
Kazuo Shizume ◽  
Tadashi Inagami

Abstract. Mouse adrenal tissue has been reported to contain high renin activity. However, it is not clear whether the renin is produced inside the tissue or is derived from a blood-borne component. We have investigated a cloned cell line of mouse adrenocortical tumour (Y-1) which has a steroidogenic activity. Sizable quantities of renin were demonstrated, predominantly in the cell lysate. This renin activity was distinguished from cathepsin D in view of its specific affinity to anti-renin antibody, optimal pH was determined, and the substrate specificity was checked with haemoglobin. Immunoreactive angiotensins were also detectable, but were demonstrated both in the cell and in the culture medium. This study provides further evidence for the existence of renin intrinsic to the adrenal gland. This study also suggests an intracellular role for renin and possible secretion of generated angiotensins.


1992 ◽  
Vol 40 (6) ◽  
pp. 737 ◽  
Author(s):  
SW Adkins

The protective conditions under which callus cultures are grown to prevent microbial contamination and to reduce tissue desiccation cause the accumulation of volatiles in the vessel headspace and reduce the availability of oxygen for respiration. To demonstrate the importance of the gaseous atmosphere to culture growth a study was undertaken on non-morphogenic rice and wheat callus incubated under a number of environmental conditions. Changes in the gaseous atmosphere above rice (Oryza sativa L.) callus during routine culture in a petri dish suppressed growth and promoted necrosis. Incubating callus under a continuous flow of gas mixtures of known composition suggested that the inhibition of growth was caused by the accumulation of high levels of ethylene and to the rapid depletion of oxygen. In order to evaluate the importance of ethylene accumulation aminoethoxyvinyl glycine (AVG), I-aminocyclopropane-I-carboxylic acid (ACC) and silver nitrate (AgNO3) were added to the nutrient medium and ethylene was measured during callus culture. Ethylene restricted callus growth particularly under high (35°C) compared with moderate (25°C) incubation temperatures and under illuminated compared with dark incubation. Under illuminated incubation at 25°C, AVG ( 5 μM ) and AgNO3 (50 μM) improved rice callus growth by 69 and 54% respectively while ACC (100 μM) decreased growth by 15%. Furthermore, rice callus growth was better in large compared with small culture vessels since ethylene accumulation was reduced. In contrast, wheat (Triticum aestivum L.) callus grew well in the petri dish system and released very little ethylene into the culture vessel headspace. Growth was better under illuminated than darkened conditions and under moderate (25°C) compared with high (35°C) incubation temperatures. Furthermore, wheat callus growth was only marginally better in large compared with small culture vessels. Ethylene was not a restrictive factor of wheat callus growth since only low levels were detected in all conditions of incubation. Better control of ethylene and increased oxygen availability could be a way of increasing cell and tissue production for genetic engineering studies of otherwise recalcitrant species such as rice, and may be a way of improving manipulation of wheat.


2012 ◽  
Vol 45 (3) ◽  
pp. 71-78
Author(s):  
Iustina Brînduşa Ciobanu ◽  
Dana Constantinovici ◽  
L. Creţu

Abstract This study was performed to reveal the changes in cell division, as a result of the prolonged period of subculture on micropropagation medium, of five local varieties of Solanum tuberosum L. maintained on in vitro collection at Suceava Genebank, Romania. For this purpose it was used the Murashige-Skoog medium (MS- 1962) with addition of 40 g/l sucrose, and 6 mg/l daminozide. The effect of prolonged period of subculture up to two and 12 months was expressed as mitotic index and frequency of cells with abnormal division. Mitotic index ranged from 20.1 to 22.1% after 12 days, between 15.5 - 17.7% after two months and between 17.7 - 19.2% after 12 months of subculture. The results obtained showed that the frequency of aberrant cells increased with the preservation time on the in vitro cultures and their accumulation rate depended on the genotype. Were identified interphases with micronuclei, metaphases with retarded chromosomes, ana-telophases with chromosomal bridges, retarded chromosomes and chromosomal fragments, but their percentage was low in all the genotypes.


2014 ◽  
Vol 62 (1-2) ◽  
pp. 43-45 ◽  
Author(s):  
Barbara Dohnal ◽  
Wanda Kisiel

The addition of an aqueous extract from fruitbodies of <i>Tylopilus felleus</i> to tissue cultures of <i>Holarrhena antidysenterica</i> (<i>Apocynaceae</i>) caused the accumulation of an unknown compound in the culture medium. The compound was isolated and identified as 5-hydroxymethyl-2-furancarboxaldehyde (1). Moreover, biosynthesis of phenolic compounds was stimulated in response to the stress agents of the fungal preparation. Methyl ferulate (2) was the major phenolic constituent.


2011 ◽  
Vol 55 (2) ◽  
pp. 181-187 ◽  
Author(s):  
Sumiyo Mimura ◽  
Naohiro Kimura ◽  
Mitsuhi Hirata ◽  
Daiki Tateyama ◽  
Midori Hayashida ◽  
...  

Development ◽  
1991 ◽  
Vol 111 (2) ◽  
pp. 635-645 ◽  
Author(s):  
K.M. Stocker ◽  
L. Sherman ◽  
S. Rees ◽  
G. Ciment

In previous studies, we showed that neural crest (NC)-derived cells from embryonic quail dorsal root ganglia (DRG) and peripheral nerve (PN), which do not normally give rise to melanocytes, become committed to melanogenesis following treatment in culture with the phorbol ester drug 12-O-tetradecanoyl phorbol-13-acetate (TPA). These and other observations support the notion that melanocytes and Schwann cells are derived from a common bipotent intermediate in the neural crest lineage—the melanocyte/Schwann cell progenitor. In this study, we test the possibility that peptide growth factors found in the embryonic environment might act similarly to TPA to influence the fates of these cells. DRG and PN explants were cultured in medium supplemented with a variety of growth factors, and then the cultures were examined for the presence of pigment cells. We found that basic fibroblast growth factor (bFGF), but not various other growth factors, induced pigmentation in about 20% of these cultures. When low concentrations of TPA were included in the culture medium, bFGF augmented the TPA-induced pigmentation, significantly increasing the proportion of pigmented cultures. These effects of bFGF were age-dependent, and could be blocked by addition of a bFGF-neutralizing antibody to the culture medium. In contrast to these stimulatory effects of bFGF, transforming growth factor-beta 1 (TGF-beta 1) was found to inhibit the TPA- or bFGF-induced pigmentation of DRG cultures. These data suggest, therefore, that at least some NC-derived cells are responsive to bFGF and TGF-beta 1, and that these growth factors may play an important role in the control of NC cell fate.


1998 ◽  
Vol 274 (1) ◽  
pp. G21-G28 ◽  
Author(s):  
Ke-Xin Liu ◽  
Yukio Kato ◽  
Tai-Ichi Kaku ◽  
Kunio Matsumoto ◽  
Toshikazu Nakamura ◽  
...  

The effect of protamine on the proliferative activity of hepatocyte growth factor (HGF) was examined in α-naphthyl isothiocyanate-intoxicated rats. Protamine preinjection increased the hepatocyte labeling index induced by HGF four- to fivefold. A similar effect was also observed in partially hepatectomized rats. Because a cell surface heparin-like substance can bind to HGF and protamine has an affinity for heparin, protamine may affect HGF pharmacokinetics. In fact, protamine injection caused a transient increase in plasma HGF concentrations after administration of HGF and, in vitro, protamine eluted HGF prebound to heparin-Sepharose. Protamine also reduced the plasma clearance of HGF and increased 2.5-fold the exposure of hepatocytes to HGF in vivo. The enhancing effect of protamine on the mitogenic response of hepatocytes to HGF was also observed in vitro (∼2-fold after protamine pretreatment compared with HGF alone), suggesting that the enhancing effect of protamine on HGF-induced liver regeneration results from dual effects exerted by protamine 1) lowering the overall elimination of HGF and 2) directly stimulating hepatocyte mitosis induced by HGF.


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