scholarly journals d ‐Lactic acid secreted by Chlorella fusca primes pattern‐triggered immunity against Pseudomonas syringae in Arabidopsis

2020 ◽  
Vol 102 (4) ◽  
pp. 761-778 ◽  
Author(s):  
Sang‐Moo Lee ◽  
Seon‐Kyu Kim ◽  
Nakyeong Lee ◽  
Chi‐Yong Ahn ◽  
Choong‐Min Ryu
2021 ◽  
Vol 291 ◽  
pp. 02006
Author(s):  
Svetlana Noskova ◽  
Stanislav Sukhikh ◽  
Olga Babich ◽  
Olga Bulgakova

Minimum inhibitory concentrations of lactic acid bacteria and other antagonist microorganisms isolated from natural sources of Kaliningrad region (soil, water bodies, plant objects) were determined. It was shown that the minimum inhibitory concentration of Pediococcus pentosaceus metabolites against Escherichia coli is 1.5·107 CFU/ml; Pseudomonas chlororaphis metabolites have no inhibitory effect against the test strain of Escherichia coli under study. It was found that Pediococcus damnosus metabolites adversely affect the growth of Escherichia coli, but at a concentration of 1.5·107 CFU/ml after 6-24 hours of cultivation. For metabolites isolated by Lactobacillus casei, the characteristic minimum inhibitory concentration with respect to the studied Escherichia coli strain is 1.5-107 CFU/ml, and for metabolites isolated by Lactobacillus fermentum, the minimum inhibitory concentration with respect to the studied Escherichia coli strain is 1.5·105 CFU/ml. At a concentration of Bacteroides hypermegas (Megamonas hypermegale) metabolites equal to 1.5·106 CFU/ml, an optical density lower than that of the control is observed. The minimum concentration of Pseudomonas syringae metabolites inhibiting Escherichia coli culture growth is 1.5-107 CFU/ml. For the metabolites Acetobacter aceti and Psychrobacter urativorans, the concentration of 1.5·107 CFU/ml is the lowest to inhibit the growth of Escherichia coli.


Author(s):  
A. W. Sedar ◽  
G. H. Bresnick

After experimetnal damage to the retina with a variety of procedures Müller cell hypertrophy and migration occurs. According to Kuwabara and others the reactive process in these injuries is evidenced by a marked increase in amount of glycogen in the Müller cells. These cells were considered originally supporting elements with fiber processes extending throughout the retina from inner limiting membrane to external limiting membrane, but are known now to have high lactic acid dehydrogenase activity and the ability to synthesize glycogen. Since the periodic acid-chromic acid-silver methenamine technique was shown to demonstrate glycogen at the electron microscope level, it was selected to react with glycogen in the fine processes of the Müller cell that ramify among the neural elements in various layers of the retina and demarcate these cells cytologically. The Rhesus monkey was chosen as an example of a well vascularized retina and the rabbit as an example of a avascular retina to explore the possibilities of the technique.


Author(s):  
D.A. Palmer ◽  
C.L. Bender

Coronatine is a non-host-specific phytotoxin produced by several members of the Pseudomonas syringae group of pathovars. The toxin acts as a virulence factor in P. syringae pv. tomato, allowing the organism to multiply to a higher population density and develop larger lesions than mutant strains unable to produce the toxin. The most prominent symptom observed in leaf tissue treated with coronatine is an intense spreading chlorosis; this has been attributed to a loss of chlorophylls a and b in tobacco. Coronatine's effects on membrane integrity and cell ultrastructure have not been previously investigated. The present study describes changes in tomato leaves in response to treatment with purified coronatine, infection by a coronatine-producing strain of P. syringae pv. tomato, and infection by a cor" mutant.In contrast to H2O-treated tissue, coronatine-treated tissue showed a diffuse chlorosis extending approximately 5 mm from the inoculation site. Leaf thickness, cell number, and cell dimensions were similar for both healthy and coronatine-treated, chlorotic tissue; however, the epidermal cell walls were consistently thicker in coronatine-treated leaves (Figs, la and lb).


2000 ◽  
Vol 27 (12) ◽  
pp. 1030-1033 ◽  
Author(s):  
M. Patel ◽  
H. Tawfik ◽  
Y. Myint ◽  
D. Brocklehurst ◽  
J. W. Nicholson

2007 ◽  
Vol 38 (8) ◽  
pp. 28
Author(s):  
DAMIAN MCNAMARA
Keyword(s):  

2002 ◽  
Vol 28 (1) ◽  
pp. 1-6 ◽  
Author(s):  
E Simova ◽  
D Beshkova ◽  
A Angelov ◽  
Ts Hristozova ◽  
G Frengova ◽  
...  

Planta Medica ◽  
2010 ◽  
Vol 76 (12) ◽  
Author(s):  
P Lorenz ◽  
S Duckstein ◽  
J Bertrams ◽  
U Meyer ◽  
F Stintzing

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