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Team:Bielefeld-Germany/Results/tvel5
From 2012.igem.org
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The clones were cultivated in minimal medium and induced with 1 % (v/v) methanol twice a day for 2 days. The supernatant of the culture was examined to active laccases by testing the enzyme activity. | The clones were cultivated in minimal medium and induced with 1 % (v/v) methanol twice a day for 2 days. The supernatant of the culture was examined to active laccases by testing the enzyme activity. | ||
| - | [[File:Bielefeld2012_TVEL5_Eppis.jpg|thumb|left|350px|Activity test of cultivation (culture 1, 2, 3) supernatant of [http://partsregistry.org/Part:BBa_K863207 BBa_K863207]. The control is the ''P. pastoris'' GS115.]] | + | [[File:Bielefeld2012_TVEL5_Eppis.jpg|thumb|left|350px|'''Figure 1:''' Activity test of cultivation (culture 1, 2, 3) supernatant of [http://partsregistry.org/Part:BBa_K863207 BBa_K863207]. The control is the ''P. pastoris'' GS115.]] |
Revision as of 01:17, 27 October 2012
Laccase TVEL5 from Trametes versicolor
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TVEL5 integrated in shuttle vector
The laccase Trametes versicolor TVEL5 BBa_K863030 was cloned with classic restriction ligation steps into the shuttle vector (BBa_K863204). This construct (BBa_K863207) was linearized and integrated into the yeast genome of P. pastoris GS115. Positive Clones with single cross over were identified by PCR as shown in the following pictures. <<<<<<<BILDER PCR (2 pieces)>>>>>>>> The clones were cultivated in minimal medium and induced with 1 % (v/v) methanol twice a day for 2 days. The supernatant of the culture was examined to active laccases by testing the enzyme activity.
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