Variation in nitrogen source utilisation by Pisolithus isolates maintained in axenic culture

Mycorrhiza ◽  
2001 ◽  
Vol 11 (1) ◽  
pp. 53-56 ◽  
Author(s):  
Ian C. Anderson ◽  
Susan M. Chambers ◽  
J. W. G. Cairney
1990 ◽  
Vol 45 (1-2) ◽  
pp. 13-18 ◽  
Author(s):  
Gerald Wurzel ◽  
Hans Becker

Abstract Ricciocarpos natans grows best on Gamborg B5 medium supplemented with 2% sucrose. Six other mineral media were less effective on the growth. During a culture period, pH of the media changed depending on the ammonium and nitrate content of the respective media. In media of a molar ratio of ammonium to nitrate of 1:1 or 1:1.9, pH first dropped from 6.0 to about 3.5 and then rose again. In media where nitrate is the only nitrogen source or where there is a ratio of ammonium to nitrate of 1:12.5, pH rose during the first two weeks and after this dropped. Differences in the light intensity (2000 an d 6000 lx) and light regime (14 h light/ 10 h dark) had no effects on the growth. The cultures produced a variety of terpenoids. The same pattern of compounds was seen in field-collected material as well as in cultivated material. The content of the terpenoids decreased on nitrogen and phosphorous-deficient media.


1974 ◽  
Vol 52 (12) ◽  
pp. 2571-2574 ◽  
Author(s):  
Frank L. Binder

Tieghemiomyces parasiticus, a biotrophic haustorial mycoparasite, makes excellent axenic growth on a glycerol – casein hydrolysate medium, while growth on a glucose – casein hydrolysate medium is equivalent to that of a control medium containing only the nitrogen source. A comparison of 14C-glucose and 14C-glycerol uptake indicates these substrates enter this mycoparasite at significantly different rates. Incorporation of 14C-glucose is extremely slow and limited, while 14C-glycerol incorporation is very rapid. Excellent axenic growth of this mycoparasite occurs when a glucose – casein hydrolysate medium is supplemented with the surface-active agent Tween 80. These findings suggest that the inability of glucose to support growth results from the inability of this substrate to readily enter the vegetative hyphae of this mycoparasite when cultured axenically.


1976 ◽  
Vol 42 (4) ◽  
pp. 993-1001 ◽  
Author(s):  
R. P. Kromann ◽  
T. R. Wilson ◽  
G. S. Cantwell

1958 ◽  
Vol 50 (3) ◽  
pp. 172-173 ◽  
Author(s):  
Glenn W. Burton ◽  
James E. Jackson ◽  
B. L. Southwell

jpa ◽  
1992 ◽  
Vol 5 (4) ◽  
pp. 607-610 ◽  
Author(s):  
K. L. Wells ◽  
W. O. Thom ◽  
H. B. Rice

Crop Science ◽  
1991 ◽  
Vol 31 (6) ◽  
pp. 1674-1680 ◽  
Author(s):  
P. H. Dernoeden ◽  
J. N. Crahay ◽  
D. B. Davis

Synthesis ◽  
2021 ◽  
Author(s):  
Xinjun Luan ◽  
Jingxun Yu

AbstractTransition-metal-catalyzed C–N bond formation is one of the most important pathways to synthesize N-heterocycles. Hydroxylamines can be transformed into a nucleophilic reagent to react with a carbon cation or coordinate with a transition metal; it can also become an electrophilic nitrogen source to react with arenes, alkenes, and alkynes. In this short review, the progress made on transition-metal-catalyzed cycloadditions with hydroxylamines as a nitrogen source is summarized.1 Introduction2 Cycloaddition To Form Aziridine Derivatives2.1 Intramolecular Cycloaddition To Form Aziridine Derivatives2.2 Intermolecular Cycloaddition To Form Aziridine Derivatives3 Cycloaddition To Form Indole Derivatives4 Cycloaddition To Form Other N-Heterocycles4.1 Aza-Heck-Type Amination Reactions4.2 Nitrene Insertion Amination Reactions4.3 Intramolecular Nucleophilic and Electrophilic Amination Reactions5 Conclusion and Outlook


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