Team:Michigan/Oil Sands June July

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Revision as of 00:17, 27 October 2010

	Sunday	Monday	Tuesday	Wednesday	Thursday	Friday	Saturday
Week 1	-	6/28/2010	6/29/2010	6/30/2010	7/1/2010	7/2/2010	-
Week 2	-	-	-	7/7/2010	7/8/2010	7/9/2010	7/10/2010
Week 3	-	7/12/2010	7/13/2010	7/14/2010	-	-	-
Week 4	-	-	-	-	-	-	-
Week 5	7/25/2010	7/26/2010	7/27/2010	7/28/2010	7/29/2010	7/30/2010	7/31/2010

Back to Oil Sands Main Notebook

6/28/2010

Pseudomonas putida KT2440 Antibiotic Resistance

Protocol for starting overnight culture from -80°C freezer
All protocols can also be found in the Protocols section of the Notebook

6/29/2010

Pseudomonas putida KT2440 Antibiotic Resistance

Protocol for making frozen stocks

6/29/2010 and 6/30/2010

Pseudomonas putida KT2440 Antibiotic Resistance

Protocol for P. putida KT2440 antibotic resistance

7/1/2010

Literature Review Napthenic Acids Composition & HPLC Analysis

Literature Review of the composition of napthenic acids in oil sands

7/2/2010

Literature Review of HPLC columns for analysis of napthenic acids

Pseudomonas putida KT2440 Antibiotic Resistance

Results

7/7/2010

Ann

Biobrick Transformation with Alex and Jennifer

Made CaCl2 solution and 100 mg/mL amphicilin stock solution according to the media section of the Wiki.
Started an overnight culture of DH5α according to the heat shock transformation protocol.
- A 12 mL culture was started because the protocol was multiplied by 4.

7/8/2010

Ann

Biobrick Transformation with Marc, Katie and Audra according to the heat shock transformation protocol

Started culture for Biobrick transformation from overnight at 2:30.
At 5:00pm the cultures had overgrown to an OD600 of 1.2.
- A 1:3 dilution of cells was performed and the cells were allowed to go through another doubling period of 20 minutes.
The OD600 was measured again and found to be around 0.500.
the cultures were placed on ice at 5:30 and allowed to chill for 20 minutes.
The washings were performed and the comp cells were resuspended in the residual CaCl2 only.
The OD600 of the comp cells without the glycerol was above 0.3 therefore the comp cells were concentrated enough.
The heat shock was performed for the following biobricks:
- BBa_179015
- BBa_179005
- BBa_145001
- BBa_117008
- BBa_117002
- BBa_103006
The cultures were placed in the 30C shaker to grow up for an hour at 30C at 9:00pm.
The cultures were plated at 10:00pm.

7/9/2010

Ann

Biobrick Transformation with Josh, Prae, Charlie according to the miniprep protocol

After 9 hours of growing at 37C, the plates did not have any colonies on them.
After 22 hours of growth plates that had grown had clear colonies.
- The positive and negative controls grew out accordingly.
- Only BBa_179015 and BBa_179005 had colonies (both from plate 1 and none from plate 2...):
  - BBa_179015 had over 100 colonies
  - BBa_179005 had 2 colonies
5 mL overnight cultures were started with 100 mg/mL AMP at 8pm from a single colony on each plate.

7/10/2010

Ann

Biobrick Transformation with Marcus, Bryce, Kilho, Josh, Charlie, Jeremy

Miniprep

Made frozen stocks from overnight culture of miniprep.
Performed miniprep on BBa_179015 and BBa_179005.
Measured DNA concentration with the Nanodrop:
- BBa_179015-11 ng/mL
- BBa_179005-40 ng/mL

Digest

Ran according to the digest protocol in the protocol section.
- Cut parts with EcoRI and PstI.
Digested at 37C for 30 minutes.

Gel

Ran according to the protocol in the protocol section.
Used 8 well comb instead of 13 well comb; the samples were too dilute too see.

7/12/2010

Ann

Biobrick Transformation with Jeremy

Gel

Reran gel from 7/10/2010
- Lane 1-Invitrogen 1 kb plus ladder
- Lane 2-Digested BBa_179005
  - Ran out of undigested BBa_179005
- Lane 3-Digested BBa_179015
- Lane 4-Uncut miniprep plasmid BBa_179015

We successfully extracted BBa_179015, T7-GFP; expected bands at 906 and 2079 were faintly seen in the gel picture above. No bands appeared for Biobrick Bba_179005, T7 promoter; this biobrick will be transformed again.

Biobrick Transformation take 2 with Jeremy

Autoclaved DI water for transformation and autoclaved sterile containers.

To autoclave sterile containers fill with DI water and decant the water before you start the culture in the container.

7/13/2010

Biobrick Transformation take 2 with Jeremy, Marcus, Josh, Kevin, Audra, Katie

Ann

This was performed according to the electroporation transformation.

Started the culture at 9:05am
Removed the culture at 12:05pm with an OD600 of 0.809
The OD600 of the comp cells were 1.2 after washing
The time constant for all electroporation were between 5.6 and 5.8 for the following biobricks
- Bba_K117008
- Bba_K117008 #2 (from resuspending remaining part left in registry in 15 uL of ultra pure water)
- Bba_K117002
- Bba_K145001
- Bba_K103006
- Bba_I719005
The cultures grew in the incubator from 2:15-4:00pm.
- The cultures started to clump after growing this time.
100 uL of cells were plated on 100 mg/mL AMP plates.

7/14/2010

Biobrick Transformation take 2

Ann

Electroporation Transformation

All of the transformation plates (minus the negative control) grew out!

We should do all transformations by electroporation from now on. Just check with the Lin Lab to make sure we can use the electroporation machine for a few hours before starting.

Miniprep

Started overnight cultures in 5 mL of LB plus 100 mg/mL AMP
- The following biobricks were started from the transformation plate:
  - Bba_K117008
  - Bba_K117002
  - Bba_K145001
  - Bba_K103006
  - Bba_I719005
- The following biobricks were started from the frozen stock in the -80°C freezer:
  - BBa_K719015

INPNC Biobrick part

We received the INPNC Biobrick (Bba_K265008) from UC Davis 2009 team. THANK YOU!!!
It was shipped on LB plates in a pMA-SK plasmid from Mr. Gene in E. coli DH5α
Since this plasmid has AMP antibiotic resistance I am pouring plates today with Marc and Kevin using 100 mg/mL AMP resistance; the culture will be streaked out tomorrow with Josh.

7/25/2010

Biobrick Transformation of suface display and pBAD

Ann

An 8 mL culture of E. coli DH5α in LB broth was produced and placed in the 30°C shaker to grow overnight.

7/26/2010

Biobrick Transformation of suface display and pBAD

Ann

Electroporation transformation

Started larger culture for comp cell preparation in 40 mL of LB in a 500 mL sterile container at 9:00am.

At 11:30am the OD600 of the culture was 0.730 and the cultures were placed on ice.

The transformation of the biobricks was performed according to the electroporation transformation protocol listed under the protocol section of this Wiki.

The biobricks removed from the registry are as follows:

E0040 (GFP)
K157013 (linker)
I0500 (pBAD)

The miniprep of I79015 was used as a positive control and a negative control was also run

The OD600 of the comp cells was not measured.

All of the time constants for the transformation were above 5.

The GFP, linker parts and the positive and negative control were plated on 100 mg/mL AMP plates. The pBAD part and negative control were plated on 50 mg/mL KAN plates.

7/27/2010

Biobrick Transformation of surface display and pBAD

Transformation Results

The GFP and linker transformation worked and many colonies grew out on the 100 mg/mL AMP plates.

The pBAD part did not grow out on the KAN plates. Upon further inspection this plasmid needs to be grown with IPTG to switch the origin of replication to a higher copy above 100 copies per cell. Otherwise, another origin of replication dominates that is less than 10 copies per cell. An antibiotic concentration of 50 mg/mL is probably too high; this transformation will have to be attempted a second time.

Miniprep of surface display

At 9:00am a 5 mL culture of the newly transformed GFP part, the newly transformed linker part, the OmpA part transformed previously and the INP from the UC Davis team were started for a miniprep in LB with 100 mg/mL AMP.

The modified miniprep protocol was used listed on the protocol section of the wiki to get a higher DNA concentration.

At 9:00pm the GFP, linker and INP parts were miniprepped. The OmpA culture had not grown out (not enough -80°C freezer stock was added) and a new culture was restarted at 11:00pm in 5 mL of LB with 100 mg/mL AMP.

Pouring Plates

More LB with 100 mg/mL AMP plates and LB with 25 mg/mL KAN plates were poured.

7/28/2010

OmpA Miniprep

The OmpA culture grew out and was miniprepped according the modified miniprep protocol at 11:30am.

Nanodrop of surface display parts

The miniprepped cultures from yesterday were nanodropped to determine the DNA concentration according to the protocol in the protocol section of the wiki:

GFP: 47.8 ng/uL
linker: 33.2 ng/uL
INP: 41.8 ng/uL
OmpA: 49.3 ng/uL

Digest of surface display parts

The following biobricks were digested according to the protocol on the wiki with the enzymes listed below:

GFP 1: XbaI and PstI
GFP 2: EcoRI and XbaI
INP 1: EcoRI and SpeI
INP 2: SpeI and PstI
Linker 1: XbaI and PstI
Linker 2: SpeI and PstI
OmpA 1: EcoRI and SpeI
OmpA 2: SpeI and PstI

Gel of Digest for surface display parts

A gel was run of the above digest with uncut plasmid as a control:

Lane 1: invitrogen 1 kb plus ladder
Lane 2: GFP cut with XbaI and PstI (GFP: 720 bp; Backbone: 2079 bp)
Lane 3: GFP cut with EcoRI and XbaI
Lane 4: uncut GFP plamid
Lane 5: INP cut with EcoRI and SpeI (INP: 924 bp; Backbone: 2550 bp)
Lane 6: INP cut with SpeI and PstI
Lane 7: uncut INP plasmid
Lane 8: Linker cut with XbaI and SpeI (Linker: 45 bp; Backbone: 2428 bp)
Lane 9: Linker cut with SpeI and PstI
Lane 10: uncut Linker plasmid
Lane 11: OmpA cut with EcoRI and SpeI (OmpA: 464 bp; Backbone: 2079 bp)
Lane 12: OmpA cut with SpeI and PstI
Lane 13: uncut OmpA plasmid

7/29/2010

Biofilm Assay in LB media

Cultures of E.coli K12, P. Putida (oilsands) and P. fluorescens (oilsands) were made in 2 mL of LB and placed in the 30C shaker to grow overnight.

7/30/2010

Biofilm Assay in LB media

Today the following was carried out: biofilm assay protocol

@ 8:10am the cultures were started from the overnight
@ 10:00am the OD600 of each culture was measured to be
- E. coli K12: 0.8
- P. fluorescens: 1.2
- P. putida: 1.0
  - These cultures were overgrown but still used for the experiment.

The results of this experiment are presented in the chart below:

There is a large error in the P. putida strain because there was the largest variation in the OD 600 of the liquid culture which also resulted in a large variation in the CV OD 600 reading.

We need to find a reference to compare our biofilms to. This could be either a strain that does not form biofilms or a strain that forms biofilms very well.

Transformation of pBAD

Marcus and Alex tried the transformation of pBAD again according to the electroporation protocol with Ann's Notes.

The recovery after electroporation was performed in 1 mL of LB with 1mM of IPTG added in order to have the pBAD part have a high copy number.

30 uL of 1M IPTG solution was added to a 25 mg/mL KAN plate and spread with sterile beads in order to keep the high copy plasmid in the pBAD part while plating.

7/30/2010

Transformation of pBAD

The transformation was successful; 30 colonies were observed on the plate. One colony was picked at 7:30 pm for a miniprep the next day and added to 5mL of LB + 25 mg/mL KAN + 1 mM IPTG to grow out in the 30C shaker.

Another culture was started of GFP from the -80C freezer stock in 5 mL of LB + 100 mg/mL AMP for a miniprep. Both the ligations with GFP did not work; as long as we are miniprepping and digesting we want to re-verify this part.

@@ Line 307: / Line 307: @@
 *Lane 1: invitrogen 1 kb plus ladder
-*Lane 2: GFP cut with XbaI and PstI (GFP: 720 bp Backbone: 2079 bp)
+*Lane 2: GFP cut with XbaI and PstI (GFP: 720 bp; Backbone: 2079 bp)
 *Lane 3: GFP cut with EcoRI and XbaI
 *Lane 4: uncut GFP plamid
-*Lane 5:INP cut with EcoRI and SpeI (INP: 924 bp backbone: 2550 bp)
+*Lane 5: INP cut with EcoRI and SpeI (INP: 924 bp; Backbone: 2550 bp)
-*Lane 6:INP cut with SpeI and PstI
+*Lane 6: INP cut with SpeI and PstI
-*Lane 7:uncut INP plasmid
+*Lane 7: uncut INP plasmid
-*Lane 8:Linker cut with XbaI and SpeI (Linker: 45 bp backbone: 2428 bp)
+*Lane 8: Linker cut with XbaI and SpeI (Linker: 45 bp; Backbone: 2428 bp)
-*Lane 9:Linker cut with SpeI and PstI
+*Lane 9: Linker cut with SpeI and PstI
 *Lane 10: uncut Linker plasmid
-*Lane 11: OmpA cut with EcoRI and SpeI (OmpA: 464 bp backbone: 2079 bp)
+*Lane 11: OmpA cut with EcoRI and SpeI (OmpA: 464 bp; Backbone: 2079 bp)
 *Lane 12: OmpA cut with SpeI and PstI
-*Lane 13:uncut OmpA plasmid
+*Lane 13: uncut OmpA plasmid
 ==7/29/2010==