scholarly journals A comparative systems analysis of polysaccharide-elicited responses inNeurospora crassareveals carbon source-specific cellular adaptations

2013 ◽  
Vol 91 (2) ◽  
pp. 275-299 ◽  
Author(s):  
J. Philipp Benz ◽  
Bryant H. Chau ◽  
Diana Zheng ◽  
Stefan Bauer ◽  
N. Louise Glass ◽  
...  
Keyword(s):  
Carbon Source ◽  
Systems Analysis ◽  
Comparative Systems

scholarly journals Reconciliation of Genome-Scale Metabolic Reconstructions for Comparative Systems Analysis

2011 ◽  
Vol 7 (3) ◽  
pp. e1001116 ◽  
Author(s):  
Matthew A. Oberhardt ◽  
Jacek Puchałka ◽  
Vítor A. P. Martins dos Santos ◽  
Jason A. Papin
Keyword(s):  
Systems Analysis ◽  
Genome Scale ◽  
Comparative Systems

scholarly journals Comparative systems analysis of the secretome of the opportunistic pathogen Aspergillus fumigatus and other Aspergillus species

2018 ◽  
Vol 8 (1) ◽  
Author(s):  
R. P. Vivek-Ananth ◽  
Karthikeyan Mohanraj ◽  
Muralidharan Vandanashree ◽  
Anupam Jhingran ◽  
James P. Craig ◽  
...  
Keyword(s):  
Aspergillus Fumigatus ◽  
Systems Analysis ◽  
Opportunistic Pathogen ◽  
Aspergillus Species ◽  
Comparative Systems

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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