Team:Buenos Aires/Results/Strains

From 2012.igem.org

(Difference between revisions)
(Strain characterization)
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== Strain characterization ==
== Strain characterization ==
-
'''bold''', a) Description of strains
+
'''a) Description of strains,'''
Through our experiments we worked with the following strains:  
Through our experiments we worked with the following strains:  
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|-
|-
|TCY 3043
|TCY 3043
-
|-H-T
+
|(-H-T)
|No fluorescence
|No fluorescence
|Negative control
|Negative control
|-
|-
|TCY 3190
|TCY 3190
-
|+H-T
+
|(+H-T)
|YFP + (Induced CFP)
|YFP + (Induced CFP)
|For coculture
|For coculture
|-
|-
|TCY 3265
|TCY 3265
-
|-H+T
+
|(-H+T)
|CFP
|CFP
|For coculture
|For coculture
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'''bold''', Table: Hystidine (H) and Tryptophane (T) auxotrophies per strain, type of fluorescence and description of most common utilization during the experiments.  
+
'''Table:''' Hystidine (H) and Tryptophane (T) auxotrophies per strain, type of fluorescence and description of most common utilization during the experiments.  
Nearly 15 other similar strains were evaluated and discarded due to several reasons (low screening potentiality; requirement of hormones for fluorescence induction; high reverting rate of auxotrophies, among others)
Nearly 15 other similar strains were evaluated and discarded due to several reasons (low screening potentiality; requirement of hormones for fluorescence induction; high reverting rate of auxotrophies, among others)

Revision as of 00:37, 16 September 2012


Strain characterization

Strain characterization

a)	Description of strains,

Through our experiments we worked with the following strains:

Strain ID Relevant Auxotrophies Fluorescence Used as
TCY 3043 (-H-T) No fluorescence Negative control
TCY 3190 (+H-T) YFP + (Induced CFP) For coculture
TCY 3265 (-H+T) CFP For coculture
TCY 3154
H+T
CFP +(induced YFP) Positive Control


Table: Hystidine (H) and Tryptophane (T) auxotrophies per strain, type of fluorescence and description of most common utilization during the experiments. 

Nearly 15 other similar strains were evaluated and discarded due to several reasons (low screening potentiality; requirement of hormones for fluorescence induction; high reverting rate of auxotrophies, among others)