Alkaloids in Stem Roots of Nicotiana tabacum and Spartium junceum Transformed by Agrobacterium rhizogenes

1987 ◽  
Vol 42 (1-2) ◽  
pp. 69-72 ◽  
Author(s):  
Michael Wink ◽  
Ludger Witte

Abstract The growth of root hairs from stems of Nicotiana tabacum and Spartium junceum was induced by Agrobacterium rhizogenes. Stem roots of Nicotiana contained nicotine and a second alkaloid, probably anabasein. Root hairs from stems of Spartium contained cytisine, N methylcytisine and anagyrine as major alkaloids. The alkaloid content of the tumors was 3-12 times higher than that of the respective healthy host tissue.

1995 ◽  
Vol 25 (2) ◽  
pp. 229-232
Author(s):  
Sergio Echeverrigaray

Morphological and proteic modifications in Nicotiana tabacum L. transformed by Agrobacterium rhizogenes were evaluated by the comparison of normal and transformant plants regenerated from hairy-roots formed by the strains A4 or IB-642 of A. rhizogenes. Changes in apical dominance were observed in IB-642 transformants, which exhibited an abnormal development of axiliary buds. The electrophoretic analysis indicated an increase in peroxidase activity and the induction of several isozymes of this complex in the transformants. The SDS-PAGE patterns comparison allows to identify several changes, specially, the increase in 31-33 and 54 kD polypeptides in the transformants.. Biochemical analysis suggests the induction of a pathogen or stress like response of the transformants due to the high auxin concentration codified by A. rhizogenes T-DNA incorporated to the plant genome.


1989 ◽  
Vol 16 (6) ◽  
pp. 517 ◽  
Author(s):  
SD Tyerman ◽  
P Oats ◽  
J Gibbs ◽  
M Dracup ◽  
H Greenway

Nicotiana tabacum plants were grown in solution culture with salinity treatments of 1, 100 and 200 mol m-3 [NaCl], in Hoagland solution. After several weeks, solute concentrations and osmotic pressure of cell sap from the roots were measured. Increases in cellular [Na+] and [Cl-] and a smaller reduction in [K+] accounted for the difference in sap osmotic pressure between the 200 mol m-3 and 1 mol m-3 treatments. Turgor pressure (P) of fully expanded cortex cells measured with the pressure probe were 0.48 MPa in 1 mol m-3, 0.24 MPa in 100 mol m-3, 0.20 MPa in 200 mol m-3, and these values agreed with those calculated by difference between internal and external osmotic pressure. Low values of volumetric elastic modulus (ε), ranging from 1.2 MPa to 3.0 MPa at P = 0.42 MPa were obtained, which accounted for long equilibration times to changes in water potential. There was no effect of high salinities on ε after accounting for the fact that ε was a function of P and neither was there an effect on hydraulic conductivity (Lp), which ranged between 1.9 × 10-8 and 24.1 × 10-8 m s-1 Mpa-1. At 200 mol m-3 [NaCl]o, and to a lesser degree at 100 mol m-3 [NaCl]o, root hairs became deformed to resemble spherical bladders (mean diameter = 88 �m) which displayed similar P and water relations to other epidermal cells and cortex cells. In other experiments the response to a sudden reduction in [NaCl], from 200 to 1 mol m-3 was studied. P of cortex cells first rapidly increased from about 0.15 MPa to 0.53 MPa and then slowly declined with a half time of about 35 min to a new steady state of 0.3 MPa. This level was maintained in intact roots for at least 48 h. The rate of the initial increase in P is limited by water flow into the cells while the slow decline is limited by solute efflux from the cells with water following osmotically. The efflux was mainly in response to reduced external osmotic pressure rather than [NaCl]o. Efflux of Na+, K+ and Cl- accounted for the decrease in internal osmotic pressure but it is possible that the membrane also became more permeable to sugars. With the exception of bladder hairs, the overall integrity of the cell membrane was maintained since Lp did not increase and P declined smoothly to the new level with no evidence of rupture and resealing of the membrane. It is argued that the loss of solutes after the step down in external osmotic pressure consists of turgor or volume regulation in which solute permeability increases steeply as turgor or volume goes above a threshold.


1994 ◽  
Vol 37 (4) ◽  
pp. 1197-1200 ◽  
Author(s):  
Luciano Barboni ◽  
Aurelio Manzi ◽  
Bice Bellomaria ◽  
Anna M. Quinto

1991 ◽  
Vol 97 (1) ◽  
pp. 212-216 ◽  
Author(s):  
Christophe Maurel ◽  
Hélène Barbier-Brygoo ◽  
Angelo Spena ◽  
Jacques Tempé ◽  
Jean Guern

1985 ◽  
Vol 186 (3) ◽  
pp. 557-564 ◽  
Author(s):  
Mylène Durand-Tardif ◽  
Richard Broglie ◽  
Jerry Slightom ◽  
David Tepfer

1991 ◽  
Vol 24 (1) ◽  
pp. 35-42 ◽  
Author(s):  
Vesna Katavić ◽  
Sibila Jelaska ◽  
Tatjana Bakran-Petricioli ◽  
Chantal David

1990 ◽  
Vol 45 (11-12) ◽  
pp. 1085-1089 ◽  
Author(s):  
Roland Greinwald ◽  
Gabriele Lurz ◽  
Ludger Witte ◽  
Franz-Christian Czygan

Abstract The alkaloid pattern of Spartium junceum has been investigated. Cytisine, N-methylcytisine, anagyrine, rhombifoline and epi-baptifoline occur as major compounds in most of the samples studied. Considerable quantitative differences were found between various parts of the plant. The alkaloid content changed strongly dependent on the seasons. Only a limited variation can be ascribed to geographical origin.


1970 ◽  
Vol 48 (1) ◽  
pp. 71-73 ◽  
Author(s):  
A. E. Harvey ◽  
J. L. Grasham

Rust mycelia from tissue cultures infected with Cronartium ribicola J. C. Fisch. ex Rabenh. were grown on cellophane membranes in the absence of physical contact with host tissue. These membranes were in contact with agar media containing imbedded, actively growing western white pine (Pinus monticola Dougl.) tissue cultures. Identities of these cultures were verified by reestablishing infections in healthy host tissue cultures.


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