July 5

From 2007.igem.org

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(Experiments)
 
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==Experiments==
==Experiments==
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1000: [5'] Transfer to 50 mL Glu M9 in 250 mL flask with [aTc]=5 ng/mL and inoculum=1,0.1 uL/mL 
 
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                          (Navneet)              (20*50=1 ug == 25 uL of 10 ug/mL)
 
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1000: [1'] Transfer to 50 mL Glu M9 in 250 mL flask with [aTc]=1 ng/mL and inoculum=1,0.1 uL/mL
 
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                          (Navneet)              (10*50=0.5 ug == 5 uL of 10 ug/mL aTc)
 
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1040: Inoculate K12z1 in 5 mL Glu M9 in 50 mL tube with [aTc]=5 ng/mL and inoculum=0.5,0.05 uL/mL
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* Open Loop [Cc]  
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                                        (20*5=0.1 ug == 2.5 uL of 10 ug/mL)
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    [5'] (Navneet)
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1040: Inoculate K12z1 in 5 mL Glu M9 in 50 mL tube with [aTc]=1 ng/mL and inoculum=0.5,0.05 uL/mL  
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i) Cells were transferred to 50 mL Glu M9 in 250 mL flask with 5 ng/mL [aTc] and 1,0.1 uL/mL of inoculum.
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                                        (10*5=0.05 ug == 0.5 uL of 10 ug/mL)
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    [1']  (Navneet)
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ii) K12z1 was inoculated in 5 mL Glu M9 in 50 mL tube with [aTc]=5 ng/mL and 0.5,0.05 uL/mL of inoculum.
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1145: [20'] Image Open loop samples   
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iii) However, right OD was not reached in time and this would be repeated.
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1230: Inoculate pL.LuxR.Y.pR.C, K12z1, pL.Y in LB  (Navneet)
 
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1400: [0] Image Open loop samples
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* Open Loop [Dd]
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1530: Inoculate pL.LuxR.Y.pR.C, K12z1 in LB  (Vivek)
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i)Cells were transferred to 50 mL Glu M9 in 250 mL flask with [aTc]=1 ng/mL and inoculum=1,0.1 uL/mL.
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2315: [1'] Filtered OD flask=0.193 (Navneet)
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ii) K12z1 was inoculated in 5 mL Glu M9 in 50 mL tube with [aTc]=1 ng/mL and inoculum=0.5,0.05 uL/mL.
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      (5' has to be repeated; right OD was not reached in time)
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iii)The flask having cells with OD=0.193 was filtered out.
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0030:    Made 7 dilutions for pL.LuxR.Y.pR.C with AI from 1 ng/mL aTc and new 2xM9 in 1:1 ratio
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* 7 dilutions with full IPTG conc range were made for pL.LuxR.Y.pR.C with AI from 1 ng/mL aTc and new 2xM9 in 1:1 ratio.
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      [1']            -ve control: K12z1 in AI from 1 ng/mL aTc and new 2xM9 in 1:1 ratio                                                         +ve control: pL.Y, 100 uM IPTG, 1x M9   (Krishna) 
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** -ve control: K12z1 in AI from 1 ng/mL aTc and new 2xM9 in 1:1 ratio
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** +ve control: pL.Y, 100 uM IPTG, 1x M9
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0105: [50'],[5'] Inoculated pT.LuxI.C, K12Z1 in L/B
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0145: [1']  Only M9, 500 uM IPTG, pL.LuxR.Y.pR.C
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            K12Z1-grown in aTc 1 medium:2x M9, 500 uM IPTG, pL.LuxR.Y.pR.C
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* To show that K12z1 does not produce any chemical in M9+aTc which might affect the system, we compared the CFP/YFP expressions of the following 2 samples: 
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** pL.LuxR.Y.pR.C was inoculated in Glu M9 with 500 uM IPTG, and
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** K12Z1 was grown in 1 ng/mL aTc and the cells were filtered out. This medium was then diluted with 2xGlu M9 in a 1:1 ratio, and pL.LuxR.Y.pR.C was inoculated in it with 500 uM IPTG.
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* pL.LuxR.Y.pR.C, K12z1, pL.Y were Inoculated in LB
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* pL.LuxR.Y.pR.C and K12z1 were inoculated in LB.
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* pT.LuxI.C, K12Z1 were inoculated in LB for open loop duplicate expts [Ee] and [Cc].
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'''Microscopy'''
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* Open loop samples [Aa] were imaged.
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* Open loop samples [Ff] were imaged.
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==Analysis==

Latest revision as of 11:28, 6 July 2007

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Experiments

  • Open Loop [Cc]

i) Cells were transferred to 50 mL Glu M9 in 250 mL flask with 5 ng/mL [aTc] and 1,0.1 uL/mL of inoculum.

ii) K12z1 was inoculated in 5 mL Glu M9 in 50 mL tube with [aTc]=5 ng/mL and 0.5,0.05 uL/mL of inoculum.

iii) However, right OD was not reached in time and this would be repeated.


  • Open Loop [Dd]

i)Cells were transferred to 50 mL Glu M9 in 250 mL flask with [aTc]=1 ng/mL and inoculum=1,0.1 uL/mL.

ii) K12z1 was inoculated in 5 mL Glu M9 in 50 mL tube with [aTc]=1 ng/mL and inoculum=0.5,0.05 uL/mL.

iii)The flask having cells with OD=0.193 was filtered out.

  • 7 dilutions with full IPTG conc range were made for pL.LuxR.Y.pR.C with AI from 1 ng/mL aTc and new 2xM9 in 1:1 ratio.
    • -ve control: K12z1 in AI from 1 ng/mL aTc and new 2xM9 in 1:1 ratio
    • +ve control: pL.Y, 100 uM IPTG, 1x M9


  • To show that K12z1 does not produce any chemical in M9+aTc which might affect the system, we compared the CFP/YFP expressions of the following 2 samples:
    • pL.LuxR.Y.pR.C was inoculated in Glu M9 with 500 uM IPTG, and
    • K12Z1 was grown in 1 ng/mL aTc and the cells were filtered out. This medium was then diluted with 2xGlu M9 in a 1:1 ratio, and pL.LuxR.Y.pR.C was inoculated in it with 500 uM IPTG.


  • pL.LuxR.Y.pR.C, K12z1, pL.Y were Inoculated in LB
  • pL.LuxR.Y.pR.C and K12z1 were inoculated in LB.
  • pT.LuxI.C, K12Z1 were inoculated in LB for open loop duplicate expts [Ee] and [Cc].


Microscopy

  • Open loop samples [Aa] were imaged.
  • Open loop samples [Ff] were imaged.


Analysis