Difference between revisions of "Part:BBa K1949100:Design"

(Materials and Methods)
Line 20: Line 20:
 
-Plasmids
 
-Plasmids
  
GFP :  Pcon - <i>rbs</i> - <i>gfp</i> (pSB6A1), Plac - <i>rbs</i> (pSB3K3)<br>
+
<i>E. coli</i> A:  Pcon - <i>rbs</i> - <i>gfp</i> (pSB6A1), Plac - <i>rbs</i> (pSB3K3)
  
MazF : PBAD - <i>rbs - mazF - tt</i> - Pcon - <i>rbs - gfp</i> (pSB6A1), Plac - <i>rbs</i> (pSB3K3)
+
<i>E. coli</i> B: PBAD - <i>rbs - mazF - tt</i> - Pcon - <i>rbs - gfp</i> (pSB6A1), Plac - <i>rbs</i> (pSB3K3)
  
 
=====Ⅱ.<i>mazEF</i> System Assay ~Stop & GO~=====
 
=====Ⅱ.<i>mazEF</i> System Assay ~Stop & GO~=====
Line 28: Line 28:
 
-Plasmids
 
-Plasmids
  
vector : PBAD - <i>rbs</i> (pSB6A1), Plac - <i>rbs</i> (pSB3K3)
+
<i>E. coli</i> C: PBAD - <i>rbs</i> (pSB6A1), Plac - <i>rbs</i> (pSB3K3)
  
GFP : Pcon - <i>rbs - gfp</i> (pSB6A1), Plac - <i>rbs</i> (pSB3K3)
+
<i>E. coli</i> A: Pcon - <i>rbs - gfp</i> (pSB6A1), Plac - <i>rbs</i> (pSB3K3)
  
MazF + MazE : PBAD - <i>rbs - mazF - tt</i> - Pcon - <i>rbs - gfp</i> (pSB6A1), Plac - <i>rbs - mazE</i> (pSB3K3)
+
<i>E. coli</i> D: PBAD - <i>rbs - mazF - tt</i> - Pcon - <i>rbs - gfp</i> (pSB6A1), Plac - <i>rbs - mazE</i> (pSB3K3)
  
MazF : PBAD - <i>rbs - mazF - tt</i> - Pcon - <i>rbs - gfp</i> (pSB6A1), Plac - <i>rbs</i> (pSB3K3)
+
<i>E. coli</i> B: PBAD - <i>rbs - mazF - tt</i> - Pcon - <i>rbs - gfp</i> (pSB6A1), Plac - <i>rbs</i> (pSB3K3)
  
=====Ⅲ.Control of Cell Growth=====
+
=====Ⅲ.<i>mazEF</i> System Assay ~Go & Stop~=====
 +
 
 +
-Plasmids
 +
 
 +
<i>E. coli</i> C: PBAD - <i>rbs</i> (pSB6A1), Plac - <i>rbs</i> (pSB3K3)
 +
 
 +
<i>E. coli</i> A: Pcon - <i>rbs - gfp</i> (pSB6A1), Plac - <i>rbs</i> (pSB3K3)
 +
 
 +
<i>E. coli</i> G: PBAD - <i>rbs - mazF - tt</i> - Pcon - <i>rbs - gfp</i> (pSB6A1), Pcon - <i>rbs</i>(weak) - <i>mazE</i> (pSB3K3)
 +
 
 +
<i>E. coli</i> F: PBAD - <i>rbs - mazF - tt</i> - Pcon - <i>rbs - gfp</i> (pSB6A1), Pcon - <i>rbs - mazE</i> (pSB3K3)
 +
 
 +
<i>E. coli</i> E: PBAD - <i>rbs - mazF - tt</i> - Pcon - <i>rbs - gfp</i> (pSB6A1), vector (pSB3K3)
 +
 
 +
=====Ⅳ.Control of Cell Growth=====
  
 
-Plasmid
 
-Plasmid
  
vector : PBAD - <i>rbs</i> (pSB6A1), Plac - <i>rbs</i> (pSB3K3)
+
<i>E. coli</i> I: PBAD - <i>rbs</i> (pSB6A1), Plac - <i>rbs</i> (pSB3K3)
  
MazF + MazE : PBAD - <i>rbs - mazF</i> (pSB6A1), Plac - <i>rbs - mazE</i> (pSB3K3)
+
<i>E. coli</i> D: PBAD - <i>rbs - mazF</i> (pSB6A1), Plac - <i>rbs - mazE</i> (pSB3K3)
  
MazF : PBAD - <i>rbs - mazF</i>(pSB6A1), Plac - <i>rbs</i> (pSB3K3)
+
<i>E. coli</i> H: PBAD - <i>rbs - mazF</i>(pSB6A1), Plac - <i>rbs</i> (pSB3K3)
  
 
====Assay protocol====
 
====Assay protocol====
=====Ⅰ.Adjustment of MazF Expression=====
+
=====Ⅰ.Adjustment of <i>mazF</i> Expression=====
  
  
Line 75: Line 89:
 
1)Measure the turbidity of the pre-cultures.
 
1)Measure the turbidity of the pre-cultures.
  
2)Dilute the pre- cultures to 1 / 30 into LB medium containing 4 mL ampicillin and kanamycin.
+
2)Dilute the pre-cultures to 1 / 30 into LB medium containing 4 mL ampicillin and kanamycin.
  
 
3)Incubate with vigorous shaking so that turbidity becomes 0.03.
 
3)Incubate with vigorous shaking so that turbidity becomes 0.03.
Line 85: Line 99:
 
6)Incubate with vigorous shaking for 24 h, and measure turbidity and RFU of GFP at the proper time.
 
6)Incubate with vigorous shaking for 24 h, and measure turbidity and RFU of GFP at the proper time.
  
 +
=====Ⅲ.<i>mazEF</i> System Assay ~Go & Stop~=====
 +
======Pre-culture======
 +
1)Suspend colonies on a master plate into LB medium containing ampicillin (50 microg / mL) and kanamycin (50 microg / mL).
 +
 +
2)Incubate with vigorous shaking for 12 h.
 +
 +
======Incubation and Assay======
 +
1)Measure the turbidity of the pre-cultures.
 +
 +
2)Dilute the pre-cultures to 1 / 30 into LB medium containing 4 mL ampicillin and kanamycin.
 +
 +
3)Incubate with vigorous shaking so that the turbidity becomes 0.03.
 +
 +
4)Add arabinose so that the final concentration becomes 0.02%.
 +
 +
5)Incubate with vigorous shaking for 24 h, and measure the turbidity and the RFU of GFP at proper times.
  
=====.Control of Cell Growth=====
+
=====.<i>mazEF</i> System Assay on the LB Agar Plate(Queen's Caprice)=====
 
1)Making LB agar medium(see Table 1.).<br>
 
1)Making LB agar medium(see Table 1.).<br>
 
[[Image:Agar medium.jpg|center|600px]]<br>
 
[[Image:Agar medium.jpg|center|600px]]<br>
[[Image:Tokyo Tech1.png|thumb|center|600px|Fig. 1. Procedure of experiment]]<br>
+
[[Image:Tokyo Tech1.png|thumb|center|600px|Fig. 1. Overview of the experiment]]<br>
 
2)<i>E. coli</i> are applied at 3 agar medium (in arabinose, in IPTG, in arabinose and IPTG)(Fig. 1.).
 
2)<i>E. coli</i> are applied at 3 agar medium (in arabinose, in IPTG, in arabinose and IPTG)(Fig. 1.).
 
   
 
   
Line 105: Line 135:
  
 
9)Overnight culture at 37°C for 24 h.
 
9)Overnight culture at 37°C for 24 h.
 +
 +
===References===
 +
1)Hazan, R., B. Sat, and H. Engelberg-Kulka. <i>Escherichia coli mazEF</i> mediated cell death is triggered by various stressful conditions. J. Bacteriol.186:3663–3669.
  
 
===References===
 
===References===
 
1)Hazan, R., B. Sat, and H. Engelberg-Kulka. <i>Escherichia coli mazEF</i> mediated cell death is triggered by various stressful conditions. J. Bacteriol.186:3663–3669.
 
1)Hazan, R., B. Sat, and H. Engelberg-Kulka. <i>Escherichia coli mazEF</i> mediated cell death is triggered by various stressful conditions. J. Bacteriol.186:3663–3669.

Revision as of 21:51, 19 October 2016


Plac-rbs-mazE


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 273
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

sequence confirmed

Materials and Methods

Construction

-Strain

All the plasmids were prepared in XL1-Blue strain.

Ⅰ.Adjustment of MazF Expression

-Plasmids

E. coli A: Pcon - rbs - gfp (pSB6A1), Plac - rbs (pSB3K3)

E. coli B: PBAD - rbs - mazF - tt - Pcon - rbs - gfp (pSB6A1), Plac - rbs (pSB3K3)

Ⅱ.mazEF System Assay ~Stop & GO~

-Plasmids

E. coli C: PBAD - rbs (pSB6A1), Plac - rbs (pSB3K3)

E. coli A: Pcon - rbs - gfp (pSB6A1), Plac - rbs (pSB3K3)

E. coli D: PBAD - rbs - mazF - tt - Pcon - rbs - gfp (pSB6A1), Plac - rbs - mazE (pSB3K3)

E. coli B: PBAD - rbs - mazF - tt - Pcon - rbs - gfp (pSB6A1), Plac - rbs (pSB3K3)

Ⅲ.mazEF System Assay ~Go & Stop~

-Plasmids

E. coli C: PBAD - rbs (pSB6A1), Plac - rbs (pSB3K3)

E. coli A: Pcon - rbs - gfp (pSB6A1), Plac - rbs (pSB3K3)

E. coli G: PBAD - rbs - mazF - tt - Pcon - rbs - gfp (pSB6A1), Pcon - rbs(weak) - mazE (pSB3K3)

E. coli F: PBAD - rbs - mazF - tt - Pcon - rbs - gfp (pSB6A1), Pcon - rbs - mazE (pSB3K3)

E. coli E: PBAD - rbs - mazF - tt - Pcon - rbs - gfp (pSB6A1), vector (pSB3K3)

Ⅳ.Control of Cell Growth

-Plasmid

E. coli I: PBAD - rbs (pSB6A1), Plac - rbs (pSB3K3)

E. coli D: PBAD - rbs - mazF (pSB6A1), Plac - rbs - mazE (pSB3K3)

E. coli H: PBAD - rbs - mazF(pSB6A1), Plac - rbs (pSB3K3)

Assay protocol

Ⅰ.Adjustment of mazF Expression
Pre-culture

1)Suspend colonies on a master plate into LB medium containing ampicillin (50 microg / mL) and kanamycin (50 microg / mL).

2)Incubate with vigorous shaking for 12 h.

Incubation and Assay

1)Measure the turbidity of the pre-cultures.

2)Dilute the pre- cultures to 1 / 30 into LB medium containing 4 mL ampicillin and kanamycin.

3)Incubate with vigorous shaking so that the turbidity becomes 0.03.

4)Add arabinose so that the final concentration becomes 0.2%, 0.02%, 0.002% 0.0002% and 0%.

5)Incubate with vigorous shaking for 24 h, and measure the turbidity and the RFU of GFP.

Ⅱ.mazEF System Assay ~Stop & GO~
Pre-culture

1)Suspend colonies on a master plate into LB medium containing ampicillin (50 microg / mL) and kanamycin (50 microg / mL).

2)Incubate with vigorous shaking for 12 h.

Incubation and Assay

1)Measure the turbidity of the pre-cultures.

2)Dilute the pre-cultures to 1 / 30 into LB medium containing 4 mL ampicillin and kanamycin.

3)Incubate with vigorous shaking so that turbidity becomes 0.03.

4)Add arabinose so that the final concentration becomes 0.02%.

5)Add IPTG until the concentration becomes 2 mM after adding arabinose.

6)Incubate with vigorous shaking for 24 h, and measure turbidity and RFU of GFP at the proper time.

Ⅲ.mazEF System Assay ~Go & Stop~
Pre-culture

1)Suspend colonies on a master plate into LB medium containing ampicillin (50 microg / mL) and kanamycin (50 microg / mL).

2)Incubate with vigorous shaking for 12 h.

Incubation and Assay

1)Measure the turbidity of the pre-cultures.

2)Dilute the pre-cultures to 1 / 30 into LB medium containing 4 mL ampicillin and kanamycin.

3)Incubate with vigorous shaking so that the turbidity becomes 0.03.

4)Add arabinose so that the final concentration becomes 0.02%.

5)Incubate with vigorous shaking for 24 h, and measure the turbidity and the RFU of GFP at proper times.

Ⅳ.mazEF System Assay on the LB Agar Plate(Queen's Caprice)

1)Making LB agar medium(see Table 1.).

Agar medium.jpg

Fig. 1. Overview of the experiment

2)E. coli are applied at 3 agar medium (in arabinose, in IPTG, in arabinose and IPTG)(Fig. 1.).

3)Overnight culture at 37°C for 24 h.

4)To confirm TA system, inoculate colonies of E. coli having plasmids at agar medium containing arabinose and IPTG.

5)Overnight culture at 37°C for 24 h.

6)Inoculate colonies of E. coli into agar medium containing arabinose.

7)Overnight culture at 37°C for 24 h.

8)Inoculate colonies of E. coli into agar medium in arabinose and IPTG.

9)Overnight culture at 37°C for 24 h.

References

1)Hazan, R., B. Sat, and H. Engelberg-Kulka. Escherichia coli mazEF mediated cell death is triggered by various stressful conditions. J. Bacteriol.186:3663–3669.

References

1)Hazan, R., B. Sat, and H. Engelberg-Kulka. Escherichia coli mazEF mediated cell death is triggered by various stressful conditions. J. Bacteriol.186:3663–3669.