Characterization of Black Bean (Phaseolus vulgarisL.) Anthocyanins

1997 ◽  
Vol 45 (9) ◽  
pp. 3395-3400 ◽  
Author(s):  
Gary R. Takeoka ◽  
Lan T. Dao ◽  
Gerhard H. Full ◽  
Rosalind Y. Wong ◽  
Leslie A. Harden ◽  
...  
Keyword(s):  
Black Bean

Purification and characterization of new phytoferritin from black bean (Phaseolus vulgaris L.) seed

2010 ◽  
Vol 147 (5) ◽  
pp. 679-688 ◽  
Author(s):  
Jianjun Deng ◽  
Xiayun Liao ◽  
Ju Hu ◽  
Xiaojing Leng ◽  
Jianjun Cheng ◽  
...  
Keyword(s):  
Phaseolus Vulgaris ◽  
Phaseolus Vulgaris L ◽  
Purification And Characterization ◽  
Black Bean

scholarly journals Development and characterization of common black bean lines resistant to anthracnose, rust and angular leaf spot in Brazil

Euphytica ◽  
2010 ◽  
Vol 176 (2) ◽  
pp. 149-156 ◽  
Author(s):  
M. R. Costa ◽  
J. P. M. Tanure ◽  
K. M. A. Arruda ◽  
J. E. S. Carneiro ◽  
M. A. Moreira ◽  
...  
Keyword(s):  
Leaf Spot ◽  
Angular Leaf Spot ◽  
Black Bean

scholarly journals Characterization of cookies formulated with rice and black bean extruded flours

2011 ◽  
Vol 1 ◽  
pp. 1645-1652 ◽  
Author(s):  
Priscila Z. Bassinello ◽  
Daniela de G.C. Freitas ◽  
José Luiz R. Ascheri ◽  
Cristina Y. Takeiti ◽  
Rosangela N. Carvalho ◽  
...  
Keyword(s):  
Black Bean

Morphological Characterization of Mycobacteriophage R1

1974 ◽  
Vol 32 ◽  
pp. 254-255
Author(s):  
B. L. Soloff ◽  
T. A. Rado
Keyword(s):  
Carbon Source ◽  
Stationary Phase ◽  
Growth Phase ◽  
Minimal Medium ◽  
Morphological Characterization ◽  
Logarithmic Growth Phase ◽  
Complete Lysis ◽  
Lysogenic Culture ◽  
Logarithmic Growth

Mycobacteriophage R1 was originally isolated from a lysogenic culture of M. butyricum. The virus was propagated on a leucine-requiring derivative of M. smegmatis, 607 leu−, isolated by nitrosoguanidine mutagenesis of typestrain ATCC 607. Growth was accomplished in a minimal medium containing glycerol and glucose as carbon source and enriched by the addition of 80 μg/ ml L-leucine. Bacteria in early logarithmic growth phase were infected with virus at a multiplicity of 5, and incubated with aeration for 8 hours. The partially lysed suspension was diluted 1:10 in growth medium and incubated for a further 8 hours. This permitted stationary phase cells to re-enter logarithmic growth and resulted in complete lysis of the culture.

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