Difference between revisions of "Part:BBa K1321334:Experience"

Revision as of 15:26, 21 October 2014

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Applications of BBa_K1321334

This part was cloned into part BBa_K1321333 by Biobrick cloning, to yield BBa_K1321336. The destination vector, containing the AraC-pBAD regulatory elements, was linearized using SpeI and PstI, and AcsAB (previously digested with XbaI and PstI) was ligated at a 1:1 ratio using the T4 ligase. The ligation mix was transformed into chemically competent DH10B Escherichia coli and plated on LB Agar+Chloramphenicol plates, then incubated overnight at 37 degrees. 50 mL Falcon tubes containing 5 ml LB supplied with 50 ug/ml Chloramphenicol were inoculated with a selection of freshly grown colonies for further restriction analysis.

The functionality of part BBa_K1321336 was assayed by inducing the system with 0.1% Arabinose in 5mL LB supplied with 1% Glucose and Chloramphenicol. Overnight incubations were set up at 30 °C and 37 °C, and both empty vector controls and un-induced controls were also assayed for cellulose production. During sonication procedures LB, soluble and non-soluble fractions were produced and kept for further analysis. Congo Red at a concentration of 20uM was added to all sonicated samples, which were further incubated for 2 hours at room temperature and static conditions to allow for Congo Red binding.

User Reviews

UNIQf8b77e73d52e872b-partinfo-00000000-QINU UNIQf8b77e73d52e872b-partinfo-00000001-QINU

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 ===Applications of BBa_K1321334===
-This part was cloned into part  BBa_K1321333 by Biobrick cloning, to yield BBa_K1321336. The destination vector, containing the AraC-pBAD regulatory elements, was linearized using SpeI and PstI and AcsAB (previously digested with XbaI and PstI) was ligated at a 1:1 ratio using the T4 ligase. The ligation mix was transformed into chemically competent DH10B Escherichia coli and plated on LB Agar+Chloramphenicol plates, then incubated overnight at 37 degrees. 50 mL Falcon tubes containing 5 ml LB supplied with 50 ug/ml Chloramphenicol were inoculated with a selection of freshly grown colonies for further restriction analysis.
+This part was cloned into part  BBa_K1321333 by Biobrick cloning, to yield BBa_K1321336. The destination vector, containing the AraC-pBAD regulatory elements, was linearized using SpeI and PstI, and AcsAB (previously digested with XbaI and PstI) was ligated at a 1:1 ratio using the T4 ligase. The ligation mix was transformed into chemically competent DH10B Escherichia coli and plated on LB Agar+Chloramphenicol plates, then incubated overnight at 37 degrees. 50 mL Falcon tubes containing 5 ml LB supplied with 50 ug/ml Chloramphenicol were inoculated with a selection of freshly grown colonies for further restriction analysis.
 The functionality of part BBa_K1321336 was assayed by inducing the system with 0.1% Arabinose in 5mL LB supplied with 1% Glucose and Chloramphenicol. Overnight incubations were set up at 30 °C and 37 °C, and both empty vector controls and un-induced controls were also assayed for cellulose production. During sonication procedures LB, soluble and non-soluble fractions were produced and kept for further analysis. Congo Red at a concentration of 20uM was added to all sonicated samples, which were further incubated for 2 hours at room temperature and static conditions to allow for Congo Red binding.