Team:Washington/Notebook

From 2010.igem.org

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-
'''Gram Positive'''
+
='''Gram Positive'''=
== '''07/06/10''' ==
== '''07/06/10''' ==
Line 580: Line 580:
*19.T59S
*19.T59S
*20.CapD CP NSS Foldit (Control)
*20.CapD CP NSS Foldit (Control)
 +
 +
='''Vectors'''=
 +
 +
=='''6/15/10'''==
 +
PCR out Lac I and F1 origin from pet29b vector
 +
 +
run following PCR reaction
 +
0.5ul forward primer
 +
0.5ul reverse primer
 +
0.5ul 25mM dNTP
 +
0.5ul pet29 plasmid
 +
0.5ul fusion DNA polymerase
 +
10ul 5x polymerase buffer
 +
37.5ul dH20
 +
 +
PCR program:
 +
· Start: 98 °C for 2 min. (melt)
 +
· Cycle 98 °C for 0.5 min (melt)
 +
· 60 °C for 0.5 min. (anneal)
 +
· 72 °C for 0.5 min.
 +
· No. of Cycles: 29
 +
· End: keep at 4 °C forever
 +
 +
Check for PCR product
 +
run product with 100bp ladder on 1.5% agarose gel
 +
load 5ul sample (or ladder) and 1ul 6x loading dye into gel
 +
 +
Miniprep psb1A3 plasmids for day 2,
 +
take six 2ml LB broth overnight growths of E. Coli with psb1A3
 +
pellet cells in centrifuge, pour of supernatant fluid.
 +
Use instructions from miniprep kit
 +
store purified psb1A3 plasmids in IGEM vector box for day 2 use
 +
 +
=='''6/16/10'''==
 +
PCR gradients for F1 and LacI
 +
10 ul reactions
 +
variables: temp (58, 65, 72) for extension and DMSO (0%, 5%, and 10%)
 +
run on 1.5% arganose gel with 1kb ladder and reactions from day 1
 +
 +
results of agarose gel
 +
F1 bands on all 72C and 65C temps, 5%DMSO at 58C, Day 1 PCR
 +
LacI all 5% DMSO, 10% DMSO 58C and 65C, Day 1
 +
PCR purified DNA placed in IGEM vector box -20C
 +
 +
=='''6/17/10'''==
 +
 +
digest PCR products to make sticky ends
 +
double digestion with EcoRI and PstI
 +
double digestion of PSB1A3 w/ EcoRI and PstI in NEB buffer 3 with BSA at 37C for 1 hours. PCR purify to remove enzymes
 +
 +
digestions
 +
5ul NEB buffer 3
 +
2ul each enzyme (EcoRI and PstI)
 +
15ul PCR purified DNA (day 1 and 1.5) or plasmid DNA
 +
.5ul BSA
 +
25.5ul dH20
 +
50ul total volume
 +
 +
ligate PCR products into plasmids (PSB1A3)
 +
10ul T4 buffer
 +
30ul PCR purified F1 digest or LacI digest
 +
15ul PCR purified psb1A3 digest
 +
43.5ul dH20
 +
1.5ul T4
 +
 +
held at rm temp. 1hour for ligation
 +
 +
place ligated plasmids into E. Coli for expression
 +
transformed into E. Coli x-10 gold series competent cells
 +
2 plates Carbacillin held at 37C
 +
 +
plate E. Coli on Ampicillin to as a selection (note death gene will ensure non-ligated products don't contaminate sample)
 +
 +
=='''6/22/10'''==
 +
 +
Isolate colonies growing on plates, place part in storage.
 +
PCR test for inserts (scrap 8 colonies from each plate)
 +
suspend colonies in 10ul dH20,
 +
run PCR with 1ul VF, 1ul VR (biobrick vectors), 5ul premixed 2x Master mix (taq polymerase, taq buffer, dNTP), and 3ul colonies suspension.
 +
 +
Run PCR on 1% arganose gel
 +
 +
Make suspension of vector expressing E. coli, use for further experiments.
 +
 +
2 colonies of F1 and LacI (each) that showed recomination in gel placed in 2ml TB with Carbicillian @37C shaker
 +
 +
=='''6/23/10'''==
 +
 +
minipreped F1 and LacI broths for sequencing, sent into sequencing at genewiz
 +
 +
 +
=='''6/24/10'''==
 +
 +
PCR out constitutive promoters (Bba_J23100, J23114, J23113) and Lac regulated promoter (R0011) use ordered primer and VF2 primer.
 +
 +
Mixed
 +
0.5ul specific primer
 +
0.5ul VF2 primer
 +
0.5ul 25mM dNTP
 +
0.5ul DNA from distribution plate
 +
0.5ul fusion DNA polymerase
 +
10ul 5x polymerase buffer
 +
37.5ul dH20
 +
 +
(note master mix of H20, buffer and dNTP was used)
 +
 +
PCR was ran as follows
 +
 +
PCR program:
 +
· Start: 98 °C for 2 min. (melt)
 +
· Cycle 98 °C for 0.5 min (melt)
 +
· 58 °C for 0.2 min. (anneal)
 +
· 72 °C for 0.5 min.
 +
· No. of Cycles: 29
 +
· End: keep at 4 °C forever
 +
 +
 +
run PCR results on 2% agarose gel to check for products.
 +
 +
Products seen on lac I regualer (R0011) and J23113, no product observed on J23100 and J23114, will wait for results of transformation to decide if rePCRing or requesting new DNA from IGEM
 +
 +
Transformed DNA from plate into x10 gold series E. Coli (15ul cells to 1ul DNA)
 +
grown in TB for 1 hour on shaker @ 37C
 +
plated onto antibiotic plates (5 amp/ 1 Kan)
 +
 +
Sequencing results of Day 3.5, both colonies show 100% homology with expected DNA from ape sequence
 +
 +
=='''6/25/10'''==
 +
 +
result of plates, growth on all constitutive promoters and on psb4A5, no growth on psb1k3 and R0011 (lac regulated promoter). 
 +
 +
Growth plates were scraped and inoculated into 2.5ml TB for overnight. These broths will be used for a glycerol stock and miniprep.
 +
 +
Plates with no growth, the psb1k3 and R0011 were re-transformed using electrophoresis and plated onto the appropriate antibiotic plate (amp and Kan)
 +
 +
Also from the growth plates suspension were made of J23100 and J23114 which were PCRed (with 5% DMSO, all other same as day 5 protocol) and ran on a 2% agarose gel.
 +
Strong band from the J23100, weak band from the J23114. 
 +
 +
-over weekened broths were spun down into pellets and glycerol stocks of J23100, J23113, J23114, psb4A5 was made.
 +
 +
=='''6/28/10'''==
 +
PCR purify PCR results and check DNA concentration using Nanodropper, low concentrations on PCR products, will proceed and adjust concentration so there is a 10 to 1 insert to vector concentration for ligations. 
 +
 +
Isolate plasmid with F1 origin and Lac I from Day 4 (minipreps, done prior for F1 and LacI, for constitutive promoters done today)
 +
Digest plasmid with SpeI and PstI (F1 with Buffer 2 and BSA)
 +
Lac I and constitutive promoters XbalI and PstI. (Buffer 2 with BSA)
 +
digestions analyzed on nanodropper,
 +
 +
Ligate the digestions. Overnight ligation at 16C
 +
10ul ligation using
 +
2ul vector
 +
6ul insert (or dH20 for control)
 +
1ul buffer
 +
1ul T4 ligase
 +
 +
=='''6/29/10'''==
 +
 +
finished ligation
 +
Chemically transformed into gold series x10 cells
 +
Express with 30ul on Ampicillin, grown at 37c overnight
 +
 +
 +
=='''6/30/10'''==
 +
growth plates, no growth on control or J23100 plates, replated with 200ul on amp/ overnight @37C
 +
 +
Check for recombinants by PCRing using VF2 and VR in Taq
 +
 +
run on 1% agarose gel
 +
 +
make a broth(s) of Day 6 E. coli colonies that show signs of recombination for miniprep tommorrow, all but 1 lacI +F1 showed recombination, made broths with carb, set @37C for overnights.
 +
 +
 +
 +
=='''7/1/10'''==
 +
 +
growth plates, 1 colony on control, colonies on J23100, PCRing with biobrick primers (VF2 and VR) to run on 1% agarose gel and make broths of colonies suspensions.
 +
 +
Minipreped  broths from J23113, J23114, and LacI constructs with F1
 +
reinvigorated broth with 1ml TB and stored @4C for latter glycerol stocks
 +
 +
Kineased T7 promoter using
 +
· i. 9uL Kinase Buffer
 +
· ii. 3uL of 10mM ATP
 +
· iii. 3uL T4 Polynucleotide Kinase
 +
· iv. 52uL ddiH2O
 +
· v. 21uL Olgio
 +
incubated @37C for 1 hour then set at 95 with a slow cooling to room temp over 1 hour (PCR protocol, 95 then -.5 per 30 seconds)
 +
Ran results on 1% agarose gel. Results showed distinct band around 100bp with a smear below
 +
 +
=='''7/2/10'''==
 +
 +
Minipreped broth of J23100
 +
 +
=='''7/6/10'''==
 +
 +
digest, ligate and inserted into X10 gold cells T7
 +
digest: digest psb1A3 with E and S (T7 ready to ligate from PCR) ?
 +
ligate:
 +
plate onto Carbicillin plate
 +
 +
=='''7/7/10'''==
 +
digest psb1A3 with F1+lacI genes, at S/P (50ul reaction)
 +
digest R0011 with X/P (50ul reaction)
 +
 +
pcr out the T7 from the X10 gold cells grown up on day 9
 +
pcr out GFP (E0040) from Igem 2009 stock
 +
digest Pcr T7 with X/P
 +
*purified GFP/ T7 contaminated during purification*
 +
 +
ran on 1% agarose gel, banding around 700 bp for GFP, and banding around 100bp for colony 1, no dna in colony 2 or 3
 +
 +
 +
overnight ligate F1+lacI with R0011/T7 hold at 16C
 +
 +
between digest and ligations made more Carbicillin plates
 +
 +
examine sequencing results of J23100/114/113.  113 good stored in Glycerol stock, re-transformed J23100/114 from earlier ligation held at -20C, plated on Carbicillin for overnight growth
 +
 +
=='''7/8/10'''==
 +
plate results F1+ j23100/j23114: no colonies on J23114 redo digestion/ligation
 +
colonies on J23100, Pcr out (on 9 july, stored at 4C)
 +
re-plated j23114 using remaing broth from recovery media
 +
transform overnights into X10 gold series and grow on Carbicillin plates
 +
miniprep T7 in psb1A3, retain some broth for glycerol stock(?)
 +
 +
 +
=='''7/9/10'''==
 +
growth plate results: R0011 w/ F1&LacI shows colonies, 1 colony on J23114, no colonies on T7 recombination.  Plates retained at 4C
 +
 +
PCR T7 and GFP, purify after (using VF2 and VR, phusion) (purfied and nanodroped afterwords, looks good)
 +
pcr chosen colonies to check for recombination (use VF2 and specific promoter, green Taq)
 +
 +
run on gel (gel results, J23100 1,2,4, J23114, R0011 1,3,4) Broths made of J23100 1,2, J23114, R0011 1,4. Placed at 4C send for sequencing?
 +
 +
=='''7/26/10'''==
 +
T7 digestion, ligation, insertion using T7, LacI+F1
 +
using T7 pcr purified VR/VF digest XP , LacI+F1 digest SP
 +
plated on Carbicillin plates at 37C
 +
 +
broths from J23100, J23114, R0011 reinvigorated and placed in 37C water bath for growth
 +
 +
=='''7/27/10'''==
 +
Miniprep broths from j23100, j23114, R0011
 +
check T7 plate for growth, select 4 colonies to check for inserts via PCR with Taq mix and gel run. Gel ran with Lac I +F1, pictures did not turn out well (need better camera/ backlight) no dicernable difference between control (F1+ lacI) and T7, all 4 showed strong bands.  Colonies 1 and 2 used for making broths held overnight at 37C in shaker waterbath.
 +
 +
=='''7/28/10'''==
 +
Nano drop Minipreps from 27 july
 +
Miniprep 2 T7 broths.
 +
Send j23100, j23114, R0011 and T7 in for sequencing.
 +
 +
=='''7/29/10'''==
 +
sequencing results, J23100 good, R0011 good, T7 questionable (send in other samples) j23114 bad, redo
 +
 +
 +
=='''7/30/10'''==
 +
ligate F1 origin in psb1A3 with j23114 using earlier digestions remains plated out portion of earlier j23114 broth
 +
 +
=='''8/2/10'''==
 +
PCRed cells ran on 1% agarose gel at 155V for 1 hour.  No good T7 (used both ends of PCR primers, causing them to bind to each other and get no results) J23114 looks good on 7 of 8 colonies ran. 2 pick (1 from old 1 ligation, 1 from new ligation) for overnight growth
 +
 +
=='''8/3/10'''==
 +
minipreped 6 colonies for sequencing, 4 T7 and 2 j23114 colonies
 +
sequencing results show j23114 cross contaminated with j23113, earlier results confirm this.  T7 checking sequence incorrect, T7 results from earlier good and used for further vector construction. 
 +
 +
=='''8/9/10'''==
 +
digest, ligate, transformation, and plate GFP into vectors
 +
transform stock vectors and plate
 +
check on status of other plasmid, other plasmids in stock
 +
 +
=='''8/10/10'''==
 +
PCR GFP colonies to check for transformation (VF/VR)
 +
overnights of good colonies, (2 sets, TB and LB) (+ and - GFP)
 +
 +
=='''8/11/10'''==
 +
make glycerol stocks of + - minus (TB)
 +
expression psb1A3 (from LB) (see note from Justin), expression stopped due to no GFP signs of Constitutive promoter (j23100) during Miniprep. 
 +
Minipreped +/ - GFP psb1A3 for latter
 +
 +
=='''8/12/10'''==
 +
send in J23114 for sequencing.
 +
PCR GFP
 +
 +
=='''8/13/10'''==
 +
digest, ligate and plate (grow at room temp over weekend) GFP vectors in psb1A3
 +
sequencing result for J23114, good... found earlier flip in J23114 and J23113 (first sequencing)... which means I tossed out the vector I needed :(
 +
 +
 +
 +
=='''8/16/10'''==
 +
ligate, digest, transformation J23114, plated after 45 minutes so could get to meeting in time, remainder of broth left in shaker overnight.
 +
pick colonies for PCR verification with GFP, J23100 no good pcr results (solid bands, but too low to have GFP included) included anyhow to see if any Green would show up.  Other PCR's had expected results (bands below F1 + lacI for J23113, above for T7 and R0011) ladder shows up week even with doubling the amount normally included...
 +
overnights GFP (TB and LB) overnight colonies from plate with no GFP (LB)
 +
 +
=='''8/17/10'''==
 +
pick colony from J23114 and PCR verify/ start overnights
 +
Glycerol stock GFP transformed vectors, J23100 not stocked due to no green pigment shown when spun down, will re-ligate on the 18th (tomorrow)
 +
 +
=='''8/18/10'''==
 +
Miniprep overnights and send to sequencing (J23114)
 +
digestions, ligate, transform J23100 and J23114 with GFP (multiple colonies so you have best for sequencing results the next day)
 +
 +
=='''8/19/10'''==
 +
PCR verification of colonies, start overnights (TB for stocks)
 +
sequencing results: j23114 good (2 and 3)
 +
 +
=='''8/20/10'''==
 +
make glycerol stocks of J23114
 +
 +
=='''8/31/10'''==
 +
grow broths from glycerol stock (in LB)
 +
meet with Justin to discuss plans
 +
 +
=='''9/1/10'''==
 +
expresssion assay
 +
notes on assay: T7 used glycerol stocks 10ul into 1ml TB all others 100ul LB overnight into 1ml TB, no stock of j23114 so no j24113 overnight or non GFP for data points. Overnights grown for 24h. +/- 10 minute, grown for 4h at 37C shaker
 +
IPTG added at 2.5h to T7 and R0011, low growth of broths, re-run assay tomorrow.  Check for .1 colony density (OD 600, clear plate, 100ul broth) before induction.
 +
PCR out vectors
 +
 +
=='''9/2/2010'''==
 +
assays psb1a3
 +
overnights grown in 1ml LB w/Carbicillin, grown for approx. 16h., 50ul transferred to 2ml TB w/Carb.  checked for colony density in broth by reading OD 600 at 3h.  all constitive above .1 OD, R0011 GFP low (.068) and GFP control low.  will induce with IPTG in 30min. and wait 4 hours for final read. 
 +
verify pcr: all but j23100 with GFP showed bands at appropriate positions. nano drop of j23100 with GFP is at 16ng/ul 
 +
re PCRing J23100 + GFP, nanodrop had around 34ng/ul
 +
made plates (carb/chlor)
 +
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Revision as of 22:41, 20 September 2010

Contents

Gram Positive

07/06/10

  • Kunkel Mutagenesis

07/07/10

  • Stained and scanned protein gel. See Chris' notes on [Friday 7/2/10][http://soslab.ee.washington.edu/igem/2010/index.php/Chris#Friday_7.2F2.2F10] for contents and order.

BioRad Micro Column Protein Prep: Expression

  • Arctic Express 13C 24H no anti, Arctic Express 13C 24H kan, DE3* 22C 24H kan, Arctic Express 37C 24H Kan. (Both CapD and CapDCP)
    • CapD 22C kan and 37C kan grew much slower than the rest. (Takes about 3 - 4hrs vs around 1.5-2 hrs for the rest.)
      • One of the two actually decreased OD after 30 minutes.
  • Induced with IPTG after reached OD600 between .7-1.0 (CapD 22C kan and 37C reached about 1.3) and incubated at given temperatures.

07/08/10

  • Made glycerol stocks for Kunkel's. Put in -80C Freezer. To be shipped for sequencing.
  • Spin down remaining proteins(CapD Artic no Anti, CapD CP Arctic no Anti, CapD* Kan 22, CapD CP* Kan 22, CapD Kan Artic, CapD CP Kan Arctic) and place in -20C, awaiting purification.

07/09/10

Protein Purification

  • Lysis
  • Bind Protein
    • Numbers 6 and 7, CapD CP Anti and CapD CP 22, respectively, had lysate form in the supernatant that had been filtered through the TALON beads.
    • Sometimes centrifuged twice after pouring out supernatant because a significant amount had not filtered through TALON beads
  • Wash Protein
    • Sometimes centrifuged twice after pouring out supernatant because a significant amount had not filtered through TALON beads
  • Elution

(Note: Desired proteins have excess histidine chain that binds to TALON beads. Imidazole has higher affinity for TALON beads, so higher imidazole concentration pushes desired protein off, allowing it to fall through filter. This is why higher and higher concentrations of imidazole are used. Cleans off undesired proteins first all the way up to, hopefully, only the desired protein.)

Electrophoresis

  • Ran two gels. #1 has ladder in well 1. #2 has ladder in well 2. 3 wells per condition being Lysate, Supernatant, Purified, in that order. SDS 6uL+6uL of substance for mix. 10uL per well.

Gel #1

  • CapD Arctic No Anti, CapD Arctic Kan, CapD* Kan 22, CapD CP* Kan 37

Gel #2

  • CapD CP Arctic No Anti, CapD CP Arctic Kan, CapD CP* Kan 22, CapD* Kan 37

07/12/10

Nano Drop (Bradford Protein Assay)

  • Create normal line with known concentrations of protein (9uL Coomassie dye, 1uL protein solution) (We used .25mM, .5mM, 1mM, 2mM)
  • Use 1uL of each protein sample with 9uL Coomassie dye and measure with program.

Overnight Glycerol Stocks

  • CapD/CapD CP TB (LB?) Kan solutions with a dab of glycerol from -80C (just scrape glycerol with pipette tip and drop into TB Kan solution).
  • Incubate in 37C shaker overnight.

Dialysis

  • Put proteins into dialysis tubes. Left in cold room overnight. (Used to reduce amount of imidazole in solution.)
    • 1. CapD Arctic no Anti
    • 2. CapD Arctic Kan
    • 3. CapD* Kan 22
    • 4. CapD* Kan 37
    • 5. CapD CP Arctic no Anti
    • 6. CapD CP Arctic Kan
    • 7. CapD CP* Kan 22
    • 8. CapD CP* Kan 37

07/13/10

Nano Drop (Bradford Protein Assay)

  • Run Nano drop to find mg/mL post-dialysis

Enzyme Assay

  • Diluted small amount of each dialyzed enzyme for Assay reaction components
  • Ran fluorescence test with plate reader
  • Got weird results (low, delayed, or no activity)

Post Assay Electrophoresis

  • Ran gel to determine protein concentrations using 1mg/mL, .5mg/mL, .25mg/mL, .125mg/mL, .0625mg/mL, and .03125mg/mL BSA as standard.
  • Will enter order of wells tomorrow once paperwork is on hand

Post-assay Gel order

  • 1) Ladder
  • 2) 1mg/mL BSA
  • 3) 0.5mg/mL BSA
  • 4) 0.125mg/mL BSA
  • 5) 0.25mg/mL BSA
  • 6) 0.06mg/mL BSA
  • 7) 0.3mg/mL BSA
  • 8) CapD Arctic no anti
  • 9) CapD Arctic Kan 13C
  • 10) CapD* Kan 22C
  • 11) CapD* Kan 37C
  • 12) CapD CP Arctic no anti
  • 13) CapD CP Arctic Kan 13C
  • 14) CapD CP* Kan 22C
  • 15) CapD CP* Kan 37C

MiniPrep

  • Done by David and Chris to obtain plasmids for PCR

7/14/10

PCR (Polymerase chain reaction)

  • Diluted Primers to 10uM (10uL of 100uM primer with 90uL of diH2O)
  • Created mixes using the recipe from Table 1a at [http://www.neb.com/nebecomm/products_intl/protocol210.asp]
    • Primers were CapDOS, CapNSS
    • Template DNA was from MiniPrep (Plasmids)
    • Added T7 reverse primer to both
    • Added Phusion DNA Polymerase last to delay reaction

Kunkel Mutagenesis Sequence

  • Checked sequences that came back for desired mutations using CLC Sequence viewer [http://www.clcbio.com/index.php?id=479]. See Google Docs form for mutation information.[http://spreadsheets.google.com/ccc?key=0AvA_ILRbNLPfdEdDUk90ZFBYYjdpU1lCTHNmRl9kMFE&hl=en#gid=0]

Overnights

  • Made 6 overnights from glycerol stocks in -80C with TB Kan CapD CP*, one control, two mutant catalytic knock outs (T2A and T2V), and three mutants (F24Y, L40R, S143R)
  • Incubate at 37C in iGEM lab

Gel

  • Dialyzed proteins seemed to be very low in concentration. (BSA standard might be twice the labeled concentration on gel)


7/15/10

IPTG Induction

  • Pulled overnight glycerol stocks to be put into TB Kan solution
  • Added 1mL of culture per 50mL flask of TB Kan, 10mL of culture per 500mL flask of TB Kan
  • Incubated at 37C until OD600 was 0.6-0.8.
  • Flasks were all incubated at 37C after induction, except the control, for about 1 hour before being moved to 22C.

7/16/10

Scan Gel

  • Post Assay Gel scanned

Colony PCR

  • Boil cells with PCR with "green mix" and +T7/-T7 primers.
  • Run on DNA gel to see if mutation occurred (determine by band size).

Spin down cells

  • 4000rpm for 20 minutes
  • Store at -20C until purification

7/26/10

Induction

  • Grew up T20S, T2V, T59N, T59Q, T59H_M61A, T59H_M61T at 37C to OD0.5-0.8
  • Induced with 500uL IPTG
  • Continue incubation for 24hrs at 22C

7/27/10

  • Concentrated purified proteins
  • Ran gel
  • Ran Bradford and Enzyme Assays
  • Spin down T20S, T2V, T59N, T59Q, T59H_M61A, T59H_M61T

7/28/10

Protein Purification

  • T59Q sat in centrifuge overnight at 4C, spun down in morning again.

7/29/10

Electrophoresis

Gel #1

  • Ladder
  • A CapDCP
  • B T2V
  • C T20S
  • D T59H_M61A
  • E T59H_M61T
  • F T59N
  • G T59Q
  • BSA 2mg/mL
  • BSA 1mg/mL
  • BSA 0.5mg/mL
  • BSA .25mg/mL
  • BSA .125mg/mL
  • BSA .0625mg/mL

Gel #2

  • Ladder
  • BSA 2mg/mL
  • BSA 1mg/mL
  • BSA 0.5mg/mL
  • 1 CapD
  • 2 CapDCP
  • 3 CapDNSS
  • 4 CapDOS
  • 5 F24Y
  • 6 L40R
  • 7 S143R
  • 8 S22I,T59Q
  • 9 S57H,M61H
  • 10 T2A
  • 11 T2V

Notes

  • De-staining started at 4 pm
  • Used up remaining possibly "bad" gels. Gels have large blue blotch at the bottom.

Enzyme Assay

  • Row A=H2O
  • Row B=L-Glutamate
  • 1 CapDCP
  • 2 T2V
  • 3 T20S
  • 4 T59H_M61A
  • 5 T59H_M61T
  • 6 T59N
  • 7 T59Q
  • 8 diH2O

7/30/10

Kunkel Mutagenesis

  • 1. CapDCP NSS
  • 2. CapDCP NSS Foldit
  • 3. CapDCP w/ Thrombin
  • 4. F24H, R356K
  • 5. G79A
  • 6. M61H
  • 7. M61N
  • 8. S22Q, T59Q
  • 9. T18L, T59Q_M61N, F452W
  • 10. T20S, T59Q_M61T
  • 11. T59Q_M61Q, F452W
  • 12. T59S_M61H
  • 13. H2O

8/2/10

  • First Kunkel's failed for unknown reasons

Kunkel Mutagenesis Attempt #2

  • 1. CapDCP NSS
  • 2. CapDCP NSS Foldit
  • 3. CapDCP w/ Thrombin
  • 4. F24H, R356K
  • 5. G79A
  • 6. M61H
  • 7. M61N
  • 8. S22Q, T59Q
  • 9. T18L, T59Q_M61N, F452W
  • 10. T20S, T59Q_M61T
  • 11. T59Q_M61Q, F452W
  • 12. T59S_M61H
  • 13. H2O

8/3/10

  • Picked Kunkel's colonies and placed into plate with LB+Kan culture.
  • Shaking in 37C room
  • Scan Gels from 7/29/10

Well Order (Four per mutation)

  • CapDCP NSS- A1-D1
  • CapDCP NSS Foldit- E1-H1
  • CapDCP w/ Thrombin- A2-D2
  • F24H, R356K- E2-H2
  • G79A- A3-D3
  • M61H- E3-H3
  • M61N- A4-D4
  • S22Q, T59Q- E4-H4
  • T18L, T59Q_M61N, F452W- A5-D5
  • T20S, T59Q_M61T- E5-H5
  • T59Q_M61Q, F452W- A6-D6
  • T59S_M61H- E6-H6

8/4/10

  • Took Kunkel's overnights out of 37C room
  • Sent Glycerol Stocks for Sequencing (100uL 20% Glycerol, 100uL cells)

8/5/10

  • Computational Work from Home

8/6/10

  • Checked all Round 2 sequences. See Google Doc for mutant information.
  • Corrected Data from Assay based on Gel #2 protein concentrations.

8/9/10

  • Autoclave 15 flasks of TB (500mL)
  • Glycerol Stock Overnights (5mL TB+Kan)
    • 1. CapD CP
    • 2. CapD CP w/ Thrombin
    • 3. CapD NSS
    • 4. CapD CP NSS
    • 5. CapD CP NSS Foldit
    • 6. T2V
    • 7. F24H, R356K
    • 8. G79A
    • 9. M61H
    • 10. M61N
    • 11. S22Q, T59Q
    • 12. T18L, T59Q, M61N, F452W
    • 13. T20S, T59Q, M61T
    • 14. T59Q, M61Q, F452W
    • 15. T59S, M61H

Remember to make glycerol stock for T2A and T2V and store in -80C

8/10/10

  • Grow up cells in 500mL TB+Kan
  • Induce with 500uL 1M IPTG once at OD 0.5-0.8
  • Incubate at 18C for 24 hours
    • 1. CapD CP
    • 2. CapD CP w/ Thrombin
    • 3. CapD NSS
    • 4. CapD CP NSS
    • 5. CapD CP NSS Foldit
    • 6. T2V
    • 7. F24H, R356K
    • 8. G79A
    • 9. M61H
    • 10. M61N
    • 11. S22Q, T59Q
    • 12. T18L, T59Q, M61N, F452W
    • 13. T20S, T59Q, M61T
    • 14. T59Q, M61Q, F452W
    • 15. T59S, M61H

G79A had super slow growth rate, about OD 0.1 after 4 hours. T18L, T59Q, M61N, F452W and T59Q, M61Q, F452W about OD 0.3 after 4 hours. G79A completed at 7:00pm.

8/11/10

  • Spin down cells 4000rpm for 20 minutes. Store in -20C.

8/12/10

  • Full Purification Process
  • Concentrate Proteins
  • Run gel of purified/concentrated proteins

8/13/10

  • Interpret protein concentration from gels (scan with Baker Lab scanner)
  • Run enzyme/H2O fluorescence assay
    • CapD NSS ran for 2 possible protein concentrations. One for the bottom two bands, one for all three. Bottom two=3BC, All three=3ABC.

L-Glutamate

      • A1.1 (CapD CP)
      • A2.2 (CapD CP w/ Thrombin)
      • A3.3BC (CapD NSS: lower two bands)
      • A4.3ABC (CapD NSS: All bands)
      • A5.4 (CapD CP NSS)
      • A6.5 (CapD CP NSS Foldit)
      • A7.6 (T2V)
      • A8.7 (F24H,R356K)
      • A9.8 (G79A)
      • A10.9 (M61H)
      • A11.10 (M61N)
      • A12.11 (S22Q,T59Q)
      • C1.12 (T18L,T59Q,M61N,F452W)
      • C2.13 (T20S,T59Q,M61T)
      • C3.14 (T59Q,M61Q,F452W)
      • C4.15 (T59S,M61H)
      • C5.Blank

H2O

      • B1.1 (CapD CP)
      • B2.2 (CapD CP w/ Thrombin)
      • B3.3BC (CapD NSS: lower two bands)
      • B4.3ABC (CapD NSS: All bands)
      • B5.4 (CapD CP NSS)
      • B6.5 (CapD CP NSS Foldit)
      • B7.6 (T2V)
      • B8.7 (F24H,R356K)
      • B9.8 (G79A)
      • B10.9 (M61H)
      • B11.10 (M61N)
      • B12.11 (S22Q,T59Q)
      • D1.12 (T18L,T59Q,M61N,F452W)
      • D2.13 (T20S,T59Q,M61T)
      • D3.14 (T59Q,M61Q,F452W)
      • D4.15 (T59S,M61H)
      • D5.Blank
  • Ran Mass spec to determine the characteristics of second band on gel

8/16/10

  • Left proteins out over weekend in ice bucket.
    • CapD NSS and CapD CP NSS Foldit both crashed out.
  • Regrow CapD NSS and CapD CP NSS Foldit
  • Gravity columns left out over weekend.
    • Recharged, but ask Justin if should use again.
  • Autoclaved 2x 500mL TB in 2L flasks

8/17/10

  • Plate Chlor+Kan for incubating transformed cells
  • Transform CJ236 cells for creating ssDNA of CapD NSS and CapD CP NSS Foldit tomorrow
  • Inoculate and grow up 500mL TB+Kan cultures of CapD NSS and CapD CP NSS Foldit. Induce with 500uL IPTG at OD 0.5-0.8
    • Induced at 2pm. Incubating at 18C in shakers at Schief lab.

8/18/10

  • Spin down cells
  • Add phage to ssDNA prep and expand culture

8/19/10

  • Purified and concentrated protein (One concentrated down to 400uL, other to 800uL, instruction mismatch with protocol)[Correct: 200uL]
    • New columns used. Covered with parafilm since can't find caps.
  • Chris harvested ssDNA for CapD NSS and CapD CP NSS Foldit

8/20/10

  • A280 came up with CapD - 6.1mg/mL and CapDCP - 3.1mg/mL
  • Running gel for protein concentrations
    • Started staining 2:12 pm
  • Flash freeze CapD and CapDCP proteins in 50uL aliquots

8/23/10

  • Ran fluorescence readings to determine correction coefficients for enzyme assay due to product/substrate quenching

Rows

    • 1. Product concentration at 10uM, Substrate decreasing 100uM to 0uM (Concentration cut in half each time, 12th well is 0uM)
    • 2. 5uM Product, Substrate decreasing 100uM to 0uM (Concentration cut in half each time, 12th well is 0uM)
    • 3. Substrate set at 100uM, Product decreasing 100uM to 0uM (Concentration cut in half each time, 12th well is 0uM)

8/24/10

  • Still searching for proper Michaelis-Menten profile. (Abandoned 8/23/10 attempt)
    • Original Excitation/Emission standard looks fine (490/520nm).
    • Tested 0.01 and 0.00001 mg/mL protein. First too high, second too low.
    • Tested serial dilution (half) enzyme from 0.01mg/mL decreasing across 12 wells. Substrate hold at 1uM.
    • Tested serial dilution (half) substrate 100uM decreasing across 12 wells (no blank). Hold enzyme at 0.001mg/mL.
    • Testing serial dilution (half) substrate 1uM decreasing across 12 wells (12 is blank). Hold enzyme at 0.0001mg/mL.
  • Kunkel's Mutagenesis

8/25/10

Reads

  • Calibration Curve (New Substrate)
    • Substrate start 1uM serial dilution (halves) across. Product start 0.1uM serial dilution (thirds) down. PMT High Sensitivity
  • Enzyme Assay (New Substrate)
    • 6 Rows. Two CapDCP, two CapD, two no enzyme. (0.0001mg/mL, 2.3nM)
    • First row of each L-Glu. Second row of each H2O.
    • Substrate start 1uM serial dilution (halves) across. PMT High Sensitivity.
  • Calibration Curve (Old Substrate)
    • Substrate start 100uM serial dilution (halves) across. Product start 1uM serial dilution (thirds) down. PMT High Sensitivity
  • Enzyme Assay (Old Substrate)
    • 3 rows. L-Glutamate in all rows. CapD 0.01mg/mL (200nM), CapD 0.0001mg/mL (2nM), and no enzyme (0nM). PMT High Sensitivity.

All Complete. Looks like good results across the board. Begin data analysis tomorrow.

8/26/10

  • Normalized Michaelis-Menten Data which better fit Substrate Inhibition Curves.
  • Gave Dr. Baker an update on results from the past month.

8/27/10

  • Presentation Slides

8/30/10

  • Dilute and Kinase Oligos
    • A1. CapDCPNF I83T
    • A2. CapDCPNF I83V
    • A3. CapDCPNF T2C
    • A4. CapDCPNF T2S
    • A5. CapDCPNF T18S_T20S
    • A6. L40A
    • A7. M61A
    • A8. M61C
    • A9. M61D
    • A10. M61G
    • A11. M61I
    • A12. M61L
    • B1. M61N
    • B2. M61S
    • B3. M61T
    • B4. M61V
    • B5. T20S_F24H
    • B6. T20S_F24Y
    • B7. Control
    • B8. Tossed
    • B9. T20S
    • B10. T59N
    • B11. T59S_M61S


  • Pipetted 3uL of 8-17 kinased oligos into eppendorf tube marked M61X

Overnights Growing at 37C

  • 1.CapDCPNFDelta
  • 2.F24A
  • 3.F24H
  • 4.F24H,T59N
  • 5.F24Y,R305K
  • 6.F24Y,T59N
  • 7.F24Y,T59N,R305K
  • 8.L40R
  • 9.L40S
  • 10.L40W
  • 11.M61S
  • 12.N23K
  • 13.N23Q
  • 14.T20A
  • 15.T20C
  • 16.T20S,T59N
  • 17.T59M
  • 18.T59N
  • 19.T59S
  • 20.CapD CP NSS Foldit (Control)

8/31/10

  • Kunkel's up to plate and incubate cells
    • 1.I83T
    • 2.I83V
    • 3.L40A
    • 4.T2C
    • 5.T2S
    • 6.T2S,T18S_T20S
    • 7.T2S,T18S_T20S,T59S_M61S
    • 8.T2S,T20S
    • 9.T18S_T20S
    • 10.T20S_F24H
    • 11.T20S_F24Y
    • 12.T20S_F24Y,T59N
    • 13.T20S,M61A
    • 14.T20S,M61C
    • 15.T20S,M61D
    • 16.T20S,M61G
    • 17.T20S,M61I
    • 18.T20S,M61L
    • 19.T20S,M61N
    • 20.T20S,M61S
    • 21.T20S,M61T
    • 22.T20S,M61V
    • 23.T59S_M61S
    • 24.Control (Blank)
    • 25.Control (Only Cells)

There is an extra plate named 22,23?. Numbering may have been skewed somewhere so one plate should end up with no colonies since nothing was put on it.

Grow up proteins(small scale) to OD600 ~0.4 and induce with 25uL IPTG.

  • 1.CapDCPNFDelta
  • 2.F24A
  • 3.F24H
  • 4.F24H,T59N
  • 5.F24Y,R305K
  • 6.F24Y,T59N
  • 7.F24Y,T59N,R305K
  • 8.L40R
  • 9.L40S
  • 10.L40W
  • 11.M61S
  • 12.N23K
  • 13.N23Q
  • 14.T20A
  • 15.T20C
  • 16.T20S,T59N
  • 17.T59M
  • 18.T59N
  • 19.T59S
  • 20.CapD CP NSS Foldit (Control)

9/1/10

Have not tested F24W, R305A

Overnight: Kunkel's Plate shake in warm room

  • 1.I83T: A1-D1
  • 2.I83V: E1-H1
  • 3.L40A: A2-D2
  • 4.T2C: E2-H2
  • 5.T2S: A3-D3
  • 6.T2S,T18S_T20S: E3-H3
  • 7.T2S,T18S_T20S,T59S_M61S: A4-D4, E12-F12
  • 8.T2S,T20S: E4-H4
  • 9.T18S_T20S: A5-D5
  • 10.T20S_F24H: E5-H5
  • 11.T20S_F24Y: A6-D6
  • 12.T20S_F24Y,T59N: E6-H6
  • 13.T20S,M61A: A7-D7
  • 14.T20S,M61C: E7-H7
  • 15.T20S,M61D: A8-D8
  • 16.T20S,M61G: E8-H8
  • 17.T20S,M61I: A9-D9
  • 18.T20S,M61L: E9-H9
  • 19.T20S,M61N: A10-D10
  • 20.T20S,M61S: E10-H10
  • 21.T20S,M61T: A11-D11
  • 22.T20S,M61V: E11-H11
  • 23.T59S_M61S: A12-D12
  • 24.Blank: E12-H12

Spin Down Cells at 4:00pm. Place in -20C

  • 1.CapDCPNFDelta
  • 2.F24A
  • 3.F24H
  • 4.F24H,T59N
  • 5.F24Y,R305K
  • 6.F24Y,T59N
  • 7.F24Y,T59N,R305K
  • 8.L40R
  • 9.L40S
  • 10.L40W
  • 11.M61S
  • 12.N23K
  • 13.N23Q
  • 14.T20A
  • 15.T20C
  • 16.T20S,T59N
  • 17.T59M
  • 18.T59N
  • 19.T59S
  • 20.CapD CP NSS Foldit (Control)

Vectors

6/15/10

PCR out Lac I and F1 origin from pet29b vector

run following PCR reaction 0.5ul forward primer 0.5ul reverse primer 0.5ul 25mM dNTP 0.5ul pet29 plasmid 0.5ul fusion DNA polymerase 10ul 5x polymerase buffer 37.5ul dH20

PCR program: · Start: 98 °C for 2 min. (melt) · Cycle 98 °C for 0.5 min (melt) · 60 °C for 0.5 min. (anneal) · 72 °C for 0.5 min. · No. of Cycles: 29 · End: keep at 4 °C forever

Check for PCR product run product with 100bp ladder on 1.5% agarose gel load 5ul sample (or ladder) and 1ul 6x loading dye into gel

Miniprep psb1A3 plasmids for day 2, take six 2ml LB broth overnight growths of E. Coli with psb1A3 pellet cells in centrifuge, pour of supernatant fluid. Use instructions from miniprep kit store purified psb1A3 plasmids in IGEM vector box for day 2 use

6/16/10

PCR gradients for F1 and LacI 10 ul reactions variables: temp (58, 65, 72) for extension and DMSO (0%, 5%, and 10%) run on 1.5% arganose gel with 1kb ladder and reactions from day 1

results of agarose gel F1 bands on all 72C and 65C temps, 5%DMSO at 58C, Day 1 PCR LacI all 5% DMSO, 10% DMSO 58C and 65C, Day 1 PCR purified DNA placed in IGEM vector box -20C

6/17/10

digest PCR products to make sticky ends double digestion with EcoRI and PstI double digestion of PSB1A3 w/ EcoRI and PstI in NEB buffer 3 with BSA at 37C for 1 hours. PCR purify to remove enzymes

digestions 5ul NEB buffer 3 2ul each enzyme (EcoRI and PstI) 15ul PCR purified DNA (day 1 and 1.5) or plasmid DNA .5ul BSA 25.5ul dH20 50ul total volume

ligate PCR products into plasmids (PSB1A3) 10ul T4 buffer 30ul PCR purified F1 digest or LacI digest 15ul PCR purified psb1A3 digest 43.5ul dH20 1.5ul T4

held at rm temp. 1hour for ligation

place ligated plasmids into E. Coli for expression transformed into E. Coli x-10 gold series competent cells 2 plates Carbacillin held at 37C

plate E. Coli on Ampicillin to as a selection (note death gene will ensure non-ligated products don't contaminate sample)

6/22/10

Isolate colonies growing on plates, place part in storage. PCR test for inserts (scrap 8 colonies from each plate) suspend colonies in 10ul dH20, run PCR with 1ul VF, 1ul VR (biobrick vectors), 5ul premixed 2x Master mix (taq polymerase, taq buffer, dNTP), and 3ul colonies suspension.

Run PCR on 1% arganose gel

Make suspension of vector expressing E. coli, use for further experiments.

2 colonies of F1 and LacI (each) that showed recomination in gel placed in 2ml TB with Carbicillian @37C shaker

6/23/10

minipreped F1 and LacI broths for sequencing, sent into sequencing at genewiz


6/24/10

PCR out constitutive promoters (Bba_J23100, J23114, J23113) and Lac regulated promoter (R0011) use ordered primer and VF2 primer.

Mixed 0.5ul specific primer 0.5ul VF2 primer 0.5ul 25mM dNTP 0.5ul DNA from distribution plate 0.5ul fusion DNA polymerase 10ul 5x polymerase buffer 37.5ul dH20

(note master mix of H20, buffer and dNTP was used)

PCR was ran as follows

PCR program: · Start: 98 °C for 2 min. (melt) · Cycle 98 °C for 0.5 min (melt) · 58 °C for 0.2 min. (anneal) · 72 °C for 0.5 min. · No. of Cycles: 29 · End: keep at 4 °C forever


run PCR results on 2% agarose gel to check for products.

Products seen on lac I regualer (R0011) and J23113, no product observed on J23100 and J23114, will wait for results of transformation to decide if rePCRing or requesting new DNA from IGEM

Transformed DNA from plate into x10 gold series E. Coli (15ul cells to 1ul DNA) grown in TB for 1 hour on shaker @ 37C plated onto antibiotic plates (5 amp/ 1 Kan)

Sequencing results of Day 3.5, both colonies show 100% homology with expected DNA from ape sequence

6/25/10

result of plates, growth on all constitutive promoters and on psb4A5, no growth on psb1k3 and R0011 (lac regulated promoter).

Growth plates were scraped and inoculated into 2.5ml TB for overnight. These broths will be used for a glycerol stock and miniprep.

Plates with no growth, the psb1k3 and R0011 were re-transformed using electrophoresis and plated onto the appropriate antibiotic plate (amp and Kan)

Also from the growth plates suspension were made of J23100 and J23114 which were PCRed (with 5% DMSO, all other same as day 5 protocol) and ran on a 2% agarose gel. Strong band from the J23100, weak band from the J23114.

-over weekened broths were spun down into pellets and glycerol stocks of J23100, J23113, J23114, psb4A5 was made.

6/28/10

PCR purify PCR results and check DNA concentration using Nanodropper, low concentrations on PCR products, will proceed and adjust concentration so there is a 10 to 1 insert to vector concentration for ligations.

Isolate plasmid with F1 origin and Lac I from Day 4 (minipreps, done prior for F1 and LacI, for constitutive promoters done today) Digest plasmid with SpeI and PstI (F1 with Buffer 2 and BSA) Lac I and constitutive promoters XbalI and PstI. (Buffer 2 with BSA) digestions analyzed on nanodropper,

Ligate the digestions. Overnight ligation at 16C 10ul ligation using 2ul vector 6ul insert (or dH20 for control) 1ul buffer 1ul T4 ligase

6/29/10

finished ligation Chemically transformed into gold series x10 cells Express with 30ul on Ampicillin, grown at 37c overnight


6/30/10

growth plates, no growth on control or J23100 plates, replated with 200ul on amp/ overnight @37C

Check for recombinants by PCRing using VF2 and VR in Taq

run on 1% agarose gel

make a broth(s) of Day 6 E. coli colonies that show signs of recombination for miniprep tommorrow, all but 1 lacI +F1 showed recombination, made broths with carb, set @37C for overnights.


7/1/10

growth plates, 1 colony on control, colonies on J23100, PCRing with biobrick primers (VF2 and VR) to run on 1% agarose gel and make broths of colonies suspensions.

Minipreped broths from J23113, J23114, and LacI constructs with F1 reinvigorated broth with 1ml TB and stored @4C for latter glycerol stocks

Kineased T7 promoter using · i. 9uL Kinase Buffer · ii. 3uL of 10mM ATP · iii. 3uL T4 Polynucleotide Kinase · iv. 52uL ddiH2O · v. 21uL Olgio incubated @37C for 1 hour then set at 95 with a slow cooling to room temp over 1 hour (PCR protocol, 95 then -.5 per 30 seconds) Ran results on 1% agarose gel. Results showed distinct band around 100bp with a smear below

7/2/10

Minipreped broth of J23100

7/6/10

digest, ligate and inserted into X10 gold cells T7 digest: digest psb1A3 with E and S (T7 ready to ligate from PCR) ? ligate: plate onto Carbicillin plate

7/7/10

digest psb1A3 with F1+lacI genes, at S/P (50ul reaction) digest R0011 with X/P (50ul reaction)

pcr out the T7 from the X10 gold cells grown up on day 9 pcr out GFP (E0040) from Igem 2009 stock digest Pcr T7 with X/P

  • purified GFP/ T7 contaminated during purification*

ran on 1% agarose gel, banding around 700 bp for GFP, and banding around 100bp for colony 1, no dna in colony 2 or 3


overnight ligate F1+lacI with R0011/T7 hold at 16C

between digest and ligations made more Carbicillin plates

examine sequencing results of J23100/114/113. 113 good stored in Glycerol stock, re-transformed J23100/114 from earlier ligation held at -20C, plated on Carbicillin for overnight growth

7/8/10

plate results F1+ j23100/j23114: no colonies on J23114 redo digestion/ligation colonies on J23100, Pcr out (on 9 july, stored at 4C) re-plated j23114 using remaing broth from recovery media transform overnights into X10 gold series and grow on Carbicillin plates miniprep T7 in psb1A3, retain some broth for glycerol stock(?)


7/9/10

growth plate results: R0011 w/ F1&LacI shows colonies, 1 colony on J23114, no colonies on T7 recombination. Plates retained at 4C

PCR T7 and GFP, purify after (using VF2 and VR, phusion) (purfied and nanodroped afterwords, looks good) pcr chosen colonies to check for recombination (use VF2 and specific promoter, green Taq)

run on gel (gel results, J23100 1,2,4, J23114, R0011 1,3,4) Broths made of J23100 1,2, J23114, R0011 1,4. Placed at 4C send for sequencing?

7/26/10

T7 digestion, ligation, insertion using T7, LacI+F1 using T7 pcr purified VR/VF digest XP , LacI+F1 digest SP plated on Carbicillin plates at 37C

broths from J23100, J23114, R0011 reinvigorated and placed in 37C water bath for growth

7/27/10

Miniprep broths from j23100, j23114, R0011 check T7 plate for growth, select 4 colonies to check for inserts via PCR with Taq mix and gel run. Gel ran with Lac I +F1, pictures did not turn out well (need better camera/ backlight) no dicernable difference between control (F1+ lacI) and T7, all 4 showed strong bands. Colonies 1 and 2 used for making broths held overnight at 37C in shaker waterbath.

7/28/10

Nano drop Minipreps from 27 july Miniprep 2 T7 broths. Send j23100, j23114, R0011 and T7 in for sequencing.

7/29/10

sequencing results, J23100 good, R0011 good, T7 questionable (send in other samples) j23114 bad, redo


7/30/10

ligate F1 origin in psb1A3 with j23114 using earlier digestions remains plated out portion of earlier j23114 broth

8/2/10

PCRed cells ran on 1% agarose gel at 155V for 1 hour. No good T7 (used both ends of PCR primers, causing them to bind to each other and get no results) J23114 looks good on 7 of 8 colonies ran. 2 pick (1 from old 1 ligation, 1 from new ligation) for overnight growth

8/3/10

minipreped 6 colonies for sequencing, 4 T7 and 2 j23114 colonies sequencing results show j23114 cross contaminated with j23113, earlier results confirm this. T7 checking sequence incorrect, T7 results from earlier good and used for further vector construction.

8/9/10

digest, ligate, transformation, and plate GFP into vectors transform stock vectors and plate check on status of other plasmid, other plasmids in stock

8/10/10

PCR GFP colonies to check for transformation (VF/VR) overnights of good colonies, (2 sets, TB and LB) (+ and - GFP)

8/11/10

make glycerol stocks of + - minus (TB) expression psb1A3 (from LB) (see note from Justin), expression stopped due to no GFP signs of Constitutive promoter (j23100) during Miniprep. Minipreped +/ - GFP psb1A3 for latter

8/12/10

send in J23114 for sequencing. PCR GFP

8/13/10

digest, ligate and plate (grow at room temp over weekend) GFP vectors in psb1A3 sequencing result for J23114, good... found earlier flip in J23114 and J23113 (first sequencing)... which means I tossed out the vector I needed :(


8/16/10

ligate, digest, transformation J23114, plated after 45 minutes so could get to meeting in time, remainder of broth left in shaker overnight. pick colonies for PCR verification with GFP, J23100 no good pcr results (solid bands, but too low to have GFP included) included anyhow to see if any Green would show up. Other PCR's had expected results (bands below F1 + lacI for J23113, above for T7 and R0011) ladder shows up week even with doubling the amount normally included... overnights GFP (TB and LB) overnight colonies from plate with no GFP (LB)

8/17/10

pick colony from J23114 and PCR verify/ start overnights Glycerol stock GFP transformed vectors, J23100 not stocked due to no green pigment shown when spun down, will re-ligate on the 18th (tomorrow)

8/18/10

Miniprep overnights and send to sequencing (J23114) digestions, ligate, transform J23100 and J23114 with GFP (multiple colonies so you have best for sequencing results the next day)

8/19/10

PCR verification of colonies, start overnights (TB for stocks) sequencing results: j23114 good (2 and 3)

8/20/10

make glycerol stocks of J23114

8/31/10

grow broths from glycerol stock (in LB) meet with Justin to discuss plans

9/1/10

expresssion assay notes on assay: T7 used glycerol stocks 10ul into 1ml TB all others 100ul LB overnight into 1ml TB, no stock of j23114 so no j24113 overnight or non GFP for data points. Overnights grown for 24h. +/- 10 minute, grown for 4h at 37C shaker IPTG added at 2.5h to T7 and R0011, low growth of broths, re-run assay tomorrow. Check for .1 colony density (OD 600, clear plate, 100ul broth) before induction. PCR out vectors

9/2/2010

assays psb1a3 overnights grown in 1ml LB w/Carbicillin, grown for approx. 16h., 50ul transferred to 2ml TB w/Carb. checked for colony density in broth by reading OD 600 at 3h. all constitive above .1 OD, R0011 GFP low (.068) and GFP control low. will induce with IPTG in 30min. and wait 4 hours for final read. verify pcr: all but j23100 with GFP showed bands at appropriate positions. nano drop of j23100 with GFP is at 16ng/ul re PCRing J23100 + GFP, nanodrop had around 34ng/ul made plates (carb/chlor)


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