Sporulation and peroxidase in Bipolaris maydis: effects of xylose and thiamine

1977 ◽  
Vol 55 (14) ◽  
pp. 1996-2000 ◽  
Author(s):  
M. O. Garraway ◽  
R. C. Evans

Sporulation of the fungus Bipolaris maydis increased and peroxidase (EC 1.11.1.7) activity decreased when xylose was added as a supplement to a basal glucose – mineral salts – agar medium containing either L-asparagine or NaNO3. With L-asparagine, thiamine–HCl (1.0 mg/ℓ) caused a significant decrease in sporulation and an increase in peroxidase activity. The magnitude of the decrease induced by thiamine–HCl in sporulation and increase in residue peroxidase activity appeared greater on a non-supplemented medium than on one supplemented with xylose. With NaNO3, the magnitude of the decrease in sporulation induced by 0.1 mg/ℓ thiamine–HCl appeared comparable whether or not the medium was supplemented with xylose, but the magnitude of the increase in residue peroxidase activity was greater without than with xylose. Quantitative determination of intracellular phenols as possible substrates for peroxidase revealed that there was no change in total phenol concentration regardless of the xylose and thiamine–HCl content of the media. The apparent inverse relationship between sporulation and peroxidase activity in B. maydis provides clues to the specific regulatory mechanisms involved in sporulation.

1999 ◽  
Vol 96 (9/10) ◽  
pp. 1608-1615
Author(s):  
T. E. Malliavin ◽  
H. Desvaux ◽  
M. A. Delsuc

Planta Medica ◽  
2011 ◽  
Vol 77 (12) ◽  
Author(s):  
M Koşar ◽  
F Göger ◽  
N Kırımer ◽  
KHC Başer

Planta Medica ◽  
2014 ◽  
Vol 80 (16) ◽  
Author(s):  
FHA Fernandes ◽  
RSA Batista ◽  
G Véras ◽  
FS Souza ◽  
ACD Medeiros

Planta Medica ◽  
2015 ◽  
Vol 81 (16) ◽  
Author(s):  
E Kaynar ◽  
A Emir ◽  
B Bozkurt ◽  
GI Kaya ◽  
MA Onur ◽  
...  

1989 ◽  
Vol 62 (04) ◽  
pp. 1043-1045 ◽  
Author(s):  
Paul F M M van Bergen ◽  
Eduard A R Knot ◽  
Jan J C Jonker ◽  
Auke C de Boer ◽  
Moniek P M de Maat

SummaryWe studied the diagnostic value of recently introduced ELISA’s for the determination of thrombin-antithrombin III (TAT) complexes, fibrin degradation products (FbDP), fibrinogen degradation products (FgDP) and total degradation products (TDP) for deep venous thrombosis (DVT) in plasma of 239 consecutive outpatients, suspected for DVT by their family doctor. DVT was confirmed by impedance plethysmography in 60 patients. Using the 95th percentile range of 42 healthy volunteers the sensitivity for the detection of DVT was: 37% for TAT, 95% for TDP, 92% for FbDP and 90% for FgDP. Specificity was: 88% for TAT, 16% for TDP, 20% for FbDP and 25% for FgDP.We conclude that these assays are of little value in the diagnosis of DVT in outpatients.


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