Transgenic tobacco cell cultures expressing a Trichoderma harzianum endochitinase gene release the enzyme into the medium

2001 ◽  
Vol 20 (1) ◽  
pp. 73-78 ◽  
Author(s):  
A. Brants ◽  
E. D. Earle
2007 ◽  
Vol 164 (4) ◽  
pp. 521-524 ◽  
Author(s):  
Elisabeth Moyano ◽  
Javier Palazón ◽  
Mercedes Bonfill ◽  
Lidia Osuna ◽  
Rosa M. Cusidó ◽  
...  

2006 ◽  
Vol 41 (3) ◽  
pp. 201-222 ◽  
Author(s):  
MAREN BODE ◽  
MATTHIAS HAAS ◽  
TANYA FAYMONVILLE ◽  
BRIGITTE THIEDE ◽  
INGOLF SCHUPHAN ◽  
...  

2009 ◽  
Vol 102 (2) ◽  
pp. 508-520 ◽  
Author(s):  
Ting-Kuo Huang ◽  
Michael A. Plesha ◽  
Bryce W. Falk ◽  
Abhaya M. Dandekar ◽  
Karen A. McDonald

Author(s):  
Charles Q. Cai ◽  
W. Michael Ainley ◽  
Trevor N. Collingwood ◽  
Robbi J. Garrison ◽  
Lisa L. Schulenberg ◽  
...  

1989 ◽  
Vol 44 (3-4) ◽  
pp. 249-254 ◽  
Author(s):  
Jochen Berlin ◽  
Bernd Martin ◽  
Jerzy Nowak ◽  
Ludger Witte ◽  
Victor Wray ◽  
...  

Abstract Im mobilized tobacco cells excreted only a small proportion of their main secondary metabolite caffeoylputrescine into the culture medium . Experiments designed to release more of the com ­ pound by permeabilization caused the loss of caffeoylputrescine, probably by oxidative reactions. Moreover, rather mild treatments with permeabilizing agents (e.g. n-propanol) resulted in severe growth inhibition. The ability of permeabilized cells to form caffeoylputrescine and other hy-droxycinnam oyl conjugates from phenylalanine decreased considerably even when such cells were still able to metabolize phenylalanine into various ethyl acetate extractable com pounds (e.g. hydroxycinnamic acids and acetophenones). The formation of new biotransformation products suggests that permeabilized cells could be used as a tool for testing the enzymatic capabilities of a cell culture.


2017 ◽  
Vol 38 (SI 2 - 6th Conf EFPP 2002) ◽  
pp. 446-448 ◽  
Author(s):  
J. Koehl ◽  
E.F. Elstner ◽  
W. Oßwald ◽  
I. Heiser

Mode of action of β-quercinin, a novel elicitin on tobacco cell suspension cultures (cvs. Bel B and Bel W3) was investigated by measuring the oxidative burst and cell death in these cell cultures. β-quercinin induced an oxidative burst comparable to that excited by zoospores from P. quercina. Adding superoxidedismutase, catalase and diphenyleneiodonium to elicited cell cultures, it could be demonstrated, that the induction of cell death in tobacco cell cultures is not correlated to the oxidative burst.


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