Team:UNIPV-Pavia/Calendar/September/settimana5

SEPTEMBER: WEEK 4

I62 and MyYeast series screening (I62, blank, MyYeastx,xbis).

I62-e was positive, so we made glycerol stock and stored it at -80°C.

Protein electrophoresis for phasins (Fede)

September, 28th

Tecan Test Giacomo

Miniprep and quantification for:

• I1: 59,6 ng/ul
• I4: 109,9 ng/ul
• I53: 160,3 ng/ul
• <partinfo>BBa_J04450</partinfo>-1:55,9 ng/ul
• <partinfo>BBa_J04450</partinfo>-2: 47 ng/ul

ON digestion of:

• I1 (E-S)
• I4 (E-S)
• I53 (E-X)
• <partinfo>BBa_J04450</partinfo>-1 (E-P)
• <partinfo>BBa_J04450</partinfo>-2 (E-P)
• MyYeast-3 (DNA already available) (E-S)
• <partinfo>pSB4C5</partinfo> (DNA already available) (E-P)

September, 29th

Tecan Test Giacomo

Colony PCR for 6 newly picked colonies.

I55 colony PCR screening (blank blank 1 ..).

No positives nor this time.

Gel run for all digested parts

Digestions (4C5 myYeast3 I4 I53 J04450-2 J04450-1 I1).

and gel run/cut/purification for:

• 4C5 (E-P): 19,3 ng/ul
• My Yeast 3 (E-S): 20,8 ng/ul
• I1: 3,8 ng/ul
• I4 (E-S): 14,2 ng/ul
• I53 (E-X): 21,6 ng/ul
• <partinfo>BBa_J04450</partinfo> (pLac-RBS-mRFP-TT) (E-P): 5,6 ng/ul
• <partinfo>pSB1C3</partinfo>: 10 ng/ul

Ligation of:

September, 30th

Tecan Test Nico

Transformation of I73 (1ul) into E. coli TOP10. It was plated on LB+Amp 100 ug/ml agar plate.

Trasformation of:

• I70 (myYeast with I4, Ptef1-mOrange-tAdh1) in TOP10 and plated on LB+Amp
• I71 (myYeast with I1, mOrange-tAdh1) in TOP10 and plated on LB+Amp
• I72 (pLac-RFP in pSB4C5) in TOP10 and plated on LB+Cm 12,5

All plates were incubated at 37°C ON

Since I55 was negative again we decided to ligate it again (probably we had a bad digest for vector - I20 - and a good one for insert - we used I38 in other ligations without problems). We diegested already miniprepped DNA for three hours with 1 ul of enzymes:

• I20: (E-X)

Gel run/cut/extraction

I20 E-X digest.

I20 E-X: ng/ul We repeated I55 ligation using newly digested vector and already digested I38 (E-S)

I55: I38 (E-S) + I20 (E-X)

Inoculum into 5ml LB+Amp of:

• I31
• I35
• I37
• I57
• I60
• INTEIN
• 3x <partinfo>BBa_J04450</partinfo> (to take <partinfo>pSB1C3</partinfo>, so <partinfo>pSB1C3</partinfo> from now on)

Cultures were let grow ON at 37°C, 220 rpm.

Inoculum of E. coli TOP10 in 1,5 ml LB, grown ON at 37çC 220 rpm. Tomorrow we will prepare competent cells!!

Inoculum of:

• S1 in 500ul M9+Cm 12,5
• I47-S1 in 500ul M9+Amp+Cm 12,5
• GFP-S1 in 500ul M9+Amp+Cm 12,5
• RBS32 in 500ul M9+Amp

Cultures were grown ON at 37°C 220 rpm.

Tomorrow we will test the ability of these str.ains to produce GFP and to lyse when HSL is added.

October, 1st

This morning, we checked tranformed plates:

I72 showed NO colony!! :/ we will repeat this ligation next week I70 and I71 showed colonies, 5 for each plate were picked and inoculated in 1ml LB+Amp to prepare glycerol stocks and for screening. I73

Transformation of I55 into E. coli DH5-alpha. It was plated on LB+Amp 100 agar plate.

Miniprep and Nanodrop quantification for:

• I31:
• I35:
• I60:

(they were also send sequencing)

• INTEIN
• <partinfo>pSB1C3</partinfo>:
• I37:
• I53:

Digest:

• <partinfo>pSB1C3</partinfo>: E-P
• <partinfo>pSB1C3</partinfo>: E-S
• <partinfo>pSB1C3</partinfo>: X-P
• INTEIN: E-P
• I60: E-S
• I31: S-P
• I35: X-P
• I37: E-X
• I57: E-X

Gel run/cut/extraction/quantification:

(foto)

• I60:
• I37:
• I57:

They were stored at -20°C

• I31:
• I35:

ON ligation of:

• IXX: I31 (S-P) + I35 (X-P) (in vector <partinfo>pSB1A2</partinfo>)
• INTEIN_C3: INTEIN (E-P) + <partinfo>pSB1C3</partinfo> (E-P)

Pick and inoculum of I73 into 5 ml LB+Amp 100. It was let grow ON at 37°C, 220 rpm.

October, 2nd