Ability to use the diazo dye, C.I. Acid Black 1 as a nitrogen source by the marine cyanobacterium Oscillatoria curviceps BDU92191

2011 ◽  
Vol 102 (14) ◽  
pp. 7218-7223 ◽  
Author(s):  
Balakrishnan Priya ◽  
Lakshmanan Uma ◽  
Abdul Khaleel Ahamed ◽  
Gopalakrishnan Subramanian ◽  
Dharmar Prabaharan
Keyword(s):  
Nitrogen Source ◽  
Marine Cyanobacterium ◽  
Diazo Dye

Effect of Iron Limitation on the Ultrastructure of Agmenellum Quadruplicatum

1981 ◽  
Vol 39 ◽  
pp. 410-411
Author(s):  
L. P. Hardie ◽  
D. L. Balkwill ◽  
S. E. Stevens
Keyword(s):  
Growth Medium ◽  
Green Alga ◽  
Natural Habitat ◽  
Iron Limitation ◽  
Natural Environments ◽  
Blue Green Alga ◽  
Marine Cyanobacterium ◽  
Natural Systems ◽  
Thin Sectioning ◽  
Agmenellum Quadruplicatum

Agmenellum quadruplicatum is a unicellular, non-nitrogen-fixing, marine cyanobacterium (blue-green alga). The ultrastructure of this organism, when grown in the laboratory with all necessary nutrients, has been characterized thoroughly. In contrast, little is known of its ultrastructure in the specific nutrient-limiting conditions typical of its natural habitat. Iron is one of the nutrients likely to limit this organism in such natural environments. It is also of great importance metabolically, being required for both photosynthesis and assimilation of nitrate. The purpose of this study was to assess the effects (if any) of iron limitation on the ultrastructure of A. quadruplicatum. It was part of a broader endeavor to elucidate the ultrastructure of cyanobacteria in natural systemsActively growing cells were placed in a growth medium containing 1% of its usual iron. The cultures were then sampled periodically for 10 days and prepared for thin sectioning TEM to assess the effects of iron limitation.

In vitro Evaluation of Ammonium Base Sulfite Liquor as an Energy and Nitrogen Source for Ruminants

1976 ◽  
Vol 42 (4) ◽  
pp. 993-1001 ◽  
Author(s):  
R. P. Kromann ◽  
T. R. Wilson ◽  
G. S. Cantwell
Keyword(s):  
Nitrogen Source ◽  
In Vitro Evaluation

Does Nitrogen Source Affect the Palatability of Coastal Bermudagrass? 1

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

Response of No-Till Corn to Nitrogen Source, Rate, and Time of Application

jpa ◽  
1992 ◽  
Vol 5 (4) ◽  
pp. 607-610 ◽  
Author(s):  
K. L. Wells ◽  
W. O. Thom ◽  
H. B. Rice
Keyword(s):  
Nitrogen Source ◽  
Time Of Application ◽  
No Till ◽  
Source Rate

Spring Dead Spot and Burmudagrass Quality As Influenced by Nitrogen Source and Potassium

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

Isolation and Total Synthesis of Bromoiesol sulfates, Antitrypanosomal arylethers from a Salileptolyngbya sp. Marine Cyanobacterium

2021 ◽  
Author(s):  
Akira Ebihara ◽  
Arihiro Iwasaki ◽  
Youhei Miura ◽  
Ghulam Jeelani ◽  
Tomoyoshi Nozaki ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Marine Cyanobacterium

Hydroxylamines as One-Atom Nitrogen Sources for Metal-Catalyzed Cycloadditions

Synthesis ◽  
2021 ◽  
Author(s):  
Xinjun Luan ◽  
Jingxun Yu
Keyword(s):  
Transition Metal ◽  
Nitrogen Source ◽  
Nucleophilic Reagent ◽  
Nitrogen Sources ◽  
Short Review ◽  
Indole Derivatives ◽  
Electrophilic Amination ◽  
Intramolecular Cycloaddition ◽  
Transition Metal Catalyzed ◽  
Metal Catalyzed

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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