Glasgow/Wetlab/Week5
From 2007.igem.org
(→Friday 3rd August 2007) |
EmmaTravis (Talk | contribs) |
||
(25 intermediate revisions not shown) | |||
Line 1: | Line 1: | ||
- | [[Glasgow|Back To Main Page]] | + | {| valign=top cellpadding=3 |
+ | |- | ||
+ | !align=center|[[Image:Uog.jpg]] || [[Glasgow|<font face=georgia color=#3366CC size=4>Back To <br> Glasgow's <br> Main Page</font>]] || [[Glasgow/Wetlab|<font face=georgia color=#3366CC size=4>Back To <br> Glasgow's <br> Wetlab Log</font>]] || [[Glasgow/Modeling|<font face=georgia color=#3366CC size=4>Go To <br> Glasgow's <br>Drylab Log</font>]] | ||
+ | |} | ||
+ | ---- | ||
+ | {|cellspacing="6px" cellpadding="16" border="0" width="100%" | ||
+ | |- align=center | ||
+ | |[https://2007.igem.org/Glasgow/Wetlab/Protocols <font face=georgia color=#3366CC size=5><b>Protocols</b></font>] | ||
+ | |[https://2007.igem.org/Glasgow/Wetlab/References <font face=georgia color=#3366CC size=5><b>References</b></font>] | ||
+ | |[https://2007.igem.org/Glasgow/Wetlab/Resources <font face=georgia color=#3366CC size=5><b>Resources</b></font>] | ||
+ | |[https://2007.igem.org/Glasgow/Wetlab/Orders <font face=georgia color=#3366CC size=5><b>Orders</b></font>] | ||
+ | |[https://2007.igem.org/Glasgow/Wetlab/Biobricks <font face=georgia color=#3366CC size=5><b>Biobricks<br>Used</b></font>] | ||
+ | |[https://2007.igem.org/Glasgow/Wetlab/Gels <font face=georgia color=#3366CC size=5><b>Gels</b></font>] | ||
+ | |} | ||
---- | ---- | ||
Line 39: | Line 52: | ||
|29, 30, 31, 33, 34, 35 | |29, 30, 31, 33, 34, 35 | ||
|- | |- | ||
- | | | + | |PhzM |
|B1 | |B1 | ||
| | | | ||
|1, 2 | |1, 2 | ||
|- | |- | ||
- | | | + | |PhzS |
|B3 | |B3 | ||
| | | | ||
|1, 2, 3 | |1, 2, 3 | ||
|- | |- | ||
- | | | + | |PhzS |
| | | | ||
- | | | + | |Bbp_PhzS_for_1 and Bbs_Oxy_2 |
|20, 21, 22 | |20, 21, 22 | ||
|- | |- | ||
- | | | + | |PhzM |
| | | | ||
- | | | + | |Bbp_PhzM_for_1 and Bbs_PhzM_rev_1 |
|23, 24, 25 | |23, 24, 25 | ||
|- | |- | ||
- | | | + | |PhzS |
| | | | ||
|Bbp_Oxy_1 and Bbs_Oxy_2 | |Bbp_Oxy_1 and Bbs_Oxy_2 | ||
|14, 15, 16 | |14, 15, 16 | ||
|- | |- | ||
- | | | + | |PhzM |
| | | | ||
|Bbp_Methyl_1 and Bbs_Methyl_2 | |Bbp_Methyl_1 and Bbs_Methyl_2 | ||
Line 108: | Line 121: | ||
Diluted new primers which arrived according to the labels. </li> | Diluted new primers which arrived according to the labels. </li> | ||
<li>Ran new PCR testing the XylR, Pr and Pu primers (original and new which arrived 30/7/07) on mt-2 with Reddymix and Touch2. Both sets of primers successful. The pGLTUR stock was unreliable.</li> | <li>Ran new PCR testing the XylR, Pr and Pu primers (original and new which arrived 30/7/07) on mt-2 with Reddymix and Touch2. Both sets of primers successful. The pGLTUR stock was unreliable.</li> | ||
- | <li>PCR of the 7 gene operon with Reddymix, Touch 2 with an extension time of 8 mins and | + | <li>PCR of the 7 gene operon with Reddymix, Touch 2 with an extension time of 8 mins and ''Pseudomonas Aeruginosa'' DNA as template. No desired bands seen. Primer combinations as follows:</li> |
- | * | + | *Bbp_PhzA_for and Bbs_PhzG_rev |
- | * | + | *Bbp_PhzA_for and Bbs_PhzD_rev |
- | * | + | *Bbp_PhzD_for and Bbs_PhzG_rev |
<li>Restriction digest (see [[Glasgow/Wetlab/Protocols#Protocol 7: Restriction Digests|Protocol 7]]) of 3/20G and 2/23N. Used Promega's AvaI for both digests and buffer B, 1hr at 37°C. Ran 10ul of the reaction with 2ul of loading dye on a 1% agarose gel. No bands showed up on the gel picture. | <li>Restriction digest (see [[Glasgow/Wetlab/Protocols#Protocol 7: Restriction Digests|Protocol 7]]) of 3/20G and 2/23N. Used Promega's AvaI for both digests and buffer B, 1hr at 37°C. Ran 10ul of the reaction with 2ul of loading dye on a 1% agarose gel. No bands showed up on the gel picture. | ||
{| border="1" cellspacing="0" cellpadding="5" align="center" | {| border="1" cellspacing="0" cellpadding="5" align="center" | ||
Line 146: | Line 159: | ||
<li> | <li> | ||
polymerase and KOD program. Amplified A-D 3.5kb and D-G 3.5kb. Primer pair as follows: | polymerase and KOD program. Amplified A-D 3.5kb and D-G 3.5kb. Primer pair as follows: | ||
- | * | + | *Bbp_PhzA_for and Bbs_PhzG_rev |
- | * | + | *Bbp_PhzA_for and Bbs_PhzD_rev |
- | * | + | *Bbp_PhzD_for and Bbs_PhzG_rev |
</li> | </li> | ||
<li> | <li> | ||
PCR (see [[Glasgow/Wetlab/Protocols#Protocol 9: PCR|Protocol 9]]) of the 7 gene operon repeated using KOD XL polymerase and KOD XL program. Amplified A-G 7kb. Primer pair as follows: | PCR (see [[Glasgow/Wetlab/Protocols#Protocol 9: PCR|Protocol 9]]) of the 7 gene operon repeated using KOD XL polymerase and KOD XL program. Amplified A-G 7kb. Primer pair as follows: | ||
- | * | + | *Bbp_PhzA_for and Bbs_PhzG_rev |
- | * | + | *Bbp_PhzA_for and Bbs_PhzD_rev |
- | * | + | *Bbp_PhzD_for and Bbs_PhzG_rev |
</li> | </li> | ||
<li> | <li> | ||
Gel ran of yesterday's BioBrick confirmation (VF2 and VR) PCR. Expected sizes and results as follows: | Gel ran of yesterday's BioBrick confirmation (VF2 and VR) PCR. Expected sizes and results as follows: | ||
+ | <br> | ||
{| border="1" cellspacing="0" cellpadding="5" align="center" | {| border="1" cellspacing="0" cellpadding="5" align="center" | ||
|'''Label''' | |'''Label''' | ||
Line 204: | Line 218: | ||
<li> | <li> | ||
Restriction digests of constructors 2/23N and 3/20G carried out again using Roche enzymes (see [[Glasgow/Wetlab/Protocols#Protocol 7: Restriction Digests|Protocol 7]]), Buffer B and incubation for at least 1hr at 37°C. All bands on gel are between 2 and 2.5 kb. Digests as follows: | Restriction digests of constructors 2/23N and 3/20G carried out again using Roche enzymes (see [[Glasgow/Wetlab/Protocols#Protocol 7: Restriction Digests|Protocol 7]]), Buffer B and incubation for at least 1hr at 37°C. All bands on gel are between 2 and 2.5 kb. Digests as follows: | ||
+ | <br> | ||
{| border="1" cellspacing="0" cellpadding="5" align="center" | {| border="1" cellspacing="0" cellpadding="5" align="center" | ||
!Constructor | !Constructor | ||
Line 240: | Line 255: | ||
#*Pu_Pre_AFT and Pu_Suf_EM | #*Pu_Pre_AFT and Pu_Suf_EM | ||
#Researched restriction maps for plasmids with death genes. | #Researched restriction maps for plasmids with death genes. | ||
- | #Overnights set up with the intention of digesting constructors of | + | #Overnights set up with the intention of digesting constructors of PhzM and PhzS after miniprepping in the morning, hopefully getting ligations that will transform TOP10 cells to grow overnight. Colonies were chosen that gave a positive result of the right predicted size (see 31/7/07) on a gel of PCR with VF2 and VR primers. |
#*4/11C constructor – 10, 11, 12 (Kan) | #*4/11C constructor – 10, 11, 12 (Kan) | ||
#*4/5I constructor – 1, 2, 3 (Carb) | #*4/5I constructor – 1, 2, 3 (Carb) | ||
#*4/5O constructor – 1, 2, 3 (Kan) | #*4/5O constructor – 1, 2, 3 (Kan) | ||
#*4/6B constructor – 2, 3 (Kan) | #*4/6B constructor – 2, 3 (Kan) | ||
- | #*B1 | + | #*B1 PhzM - 17, 18, 19, 26 (Carb) |
- | #*B3 | + | #*B3 PhzS - 20 (Carb) |
- | #*C5 | + | #*C5 PhzM - 24, 25 (Carb) |
#Miller Assay was performed (according to [[Glasgow/Wetlab/Protocols#Protocol 10: Miller Assay|Protocol 10]]) on ''E. coli'' cell culture aliquots containing the DntR system grown up in LB. A range of salicylate concentrations (0 mM, 20 uM, 50 uM, 100 uM and 200 uM)were added to aliqouts and then allowed to grow for a further 3 hours. As this was a trial run, measurements at only one time point (58 minutes) were taken. The spectrophotometer readings and their corresponding calculated Miller units are shown in the table below. | #Miller Assay was performed (according to [[Glasgow/Wetlab/Protocols#Protocol 10: Miller Assay|Protocol 10]]) on ''E. coli'' cell culture aliquots containing the DntR system grown up in LB. A range of salicylate concentrations (0 mM, 20 uM, 50 uM, 100 uM and 200 uM)were added to aliqouts and then allowed to grow for a further 3 hours. As this was a trial run, measurements at only one time point (58 minutes) were taken. The spectrophotometer readings and their corresponding calculated Miller units are shown in the table below. | ||
Line 290: | Line 305: | ||
=== Thursday 2nd August 2007 === | === Thursday 2nd August 2007 === | ||
#Minimal media prepared for the Miller Assay because it does not interfere with enzyme activity (see [[Glasgow/Wetlab/Protocols#Protocol 10: Miller Assay|Protocol 10]]). | #Minimal media prepared for the Miller Assay because it does not interfere with enzyme activity (see [[Glasgow/Wetlab/Protocols#Protocol 10: Miller Assay|Protocol 10]]). | ||
- | #Minipreps (see [[Glasgow/Wetlab/Protocols#Protocol 5: Qiagen Minipreps|Protocol 5]]) done of yesterday's overnights for | + | #Minipreps (see [[Glasgow/Wetlab/Protocols#Protocol 5: Qiagen Minipreps|Protocol 5]]) done of yesterday's overnights for PhzM and PhzS. |
- | #Digestions (see [[Glasgow/Wetlab/Protocols#Protocol 7: Restriction Digests|Protocol 7]]) done of these | + | #Digestions (see [[Glasgow/Wetlab/Protocols#Protocol 7: Restriction Digests|Protocol 7]]) done of these PhzM and PhzS minipreps: |
<br> | <br> | ||
{| border="1" cellspacing="0" cellpadding="5" align="center" | {| border="1" cellspacing="0" cellpadding="5" align="center" | ||
Line 303: | Line 318: | ||
!Results | !Results | ||
|- | |- | ||
- | | | + | |PhzM |
|B1 | |B1 | ||
|17, 18, 19, 26 | |17, 18, 19, 26 | ||
- | | | + | |PhzM_for_1 + Methyl_2 |
|PstI | |PstI | ||
|4243bp, 443bp, 275bp | |4243bp, 443bp, 275bp | ||
Line 312: | Line 327: | ||
|17, 18 + 26 possibly in orientation 1 | |17, 18 + 26 possibly in orientation 1 | ||
|- | |- | ||
- | | | + | |PhzM |
|B1 | |B1 | ||
|17, 18, 19, 26 | |17, 18, 19, 26 | ||
- | | | + | |PhzM_for_1 + Methyl_2 |
|EcoRI | |EcoRI | ||
|3654bp, 1287bp, 18bp | |3654bp, 1287bp, 18bp | ||
Line 321: | Line 336: | ||
|17, 18 + 26 possibly in orientation 1 | |17, 18 + 26 possibly in orientation 1 | ||
|- | |- | ||
- | | | + | |PhzM |
|C5 | |C5 | ||
|24, 25 | |24, 25 | ||
- | | | + | |PhzM_for_1 + PhzM_rev_1 |
|PstI | |PstI | ||
|4243bp, 443bp, 275bp | |4243bp, 443bp, 275bp | ||
Line 330: | Line 345: | ||
|Appears wrong | |Appears wrong | ||
|- | |- | ||
- | | | + | |PhzM |
|C5 | |C5 | ||
|24, 25 | |24, 25 | ||
- | | | + | |PhzM_for_1 + PhzM_rev_1 |
|EcoRI | |EcoRI | ||
|4243bp, 443bp, 275bp | |4243bp, 443bp, 275bp | ||
Line 339: | Line 354: | ||
|Possibly in orientation 1 | |Possibly in orientation 1 | ||
|- | |- | ||
- | | | + | |PhzS |
|B3 | |B3 | ||
|20 | |20 | ||
- | | | + | |PhzS_for_1 + Oxy_2 |
|PstI | |PstI | ||
|4012bp, 534bp, 344bp, 275bp | |4012bp, 534bp, 344bp, 275bp | ||
Line 348: | Line 363: | ||
|Possibly in orientation 1 | |Possibly in orientation 1 | ||
|- | |- | ||
- | | | + | |PhzS |
|B3 | |B3 | ||
|20 | |20 | ||
- | | | + | |PhzS_for_1 + Oxy_2 |
|EcoI | |EcoI | ||
|3656bp, 1491bp, 18bp | |3656bp, 1491bp, 18bp | ||
Line 389: | Line 404: | ||
<ol start="5"> | <ol start="5"> | ||
<li> | <li> | ||
- | PCR (see [[Glasgow/Wetlab/Protocols#Protocol 9: PCR|Protocol 9]]) also done (using the primers used to create the cloned versions of | + | PCR (see [[Glasgow/Wetlab/Protocols#Protocol 9: PCR|Protocol 9]]) also done (using the primers used to create the cloned versions of PhzM and PhzS) on minipreps, done this morning, of TOPO cloning (hopefully containing PhzM and PhzS) to confirm that the insert is genuinely there. Used Reddymix and Touch2. All constructs appear to contain the correct genes. |
</li> | </li> | ||
</ol> | </ol> | ||
Line 401: | Line 416: | ||
!Results | !Results | ||
|- | |- | ||
- | | | + | |PhzM |
|B1 | |B1 | ||
|17, 18, 19, 26 | |17, 18, 19, 26 | ||
- | | | + | |PhzM_for_1 + Bbs_Methyl_2 |
|1072bp | |1072bp | ||
|Appears correct | |Appears correct | ||
|- | |- | ||
- | | | + | |PhzS |
|B3 | |B3 | ||
|20 | |20 | ||
- | | | + | |PhzS_for_1 + Oxy_2 |
|1220bp | |1220bp | ||
|Appears correct | |Appears correct | ||
|- | |- | ||
- | | | + | |PhzM |
|C5 | |C5 | ||
|24, 25 | |24, 25 | ||
- | | | + | |PhzM_for_1 + PhzM_rev_1 |
|1225bp | |1225bp | ||
|24 possibly too big, 25 appears wrong | |24 possibly too big, 25 appears wrong | ||
Line 425: | Line 440: | ||
=== Friday 3rd August 2007 === | === Friday 3rd August 2007 === | ||
#Miller assay (see [[Glasgow/Wetlab/Protocols#Protocol 10: Miller Assay|Protocol 10]]) repeated on ''E.coli'' cultures grown up in minimal media. Measurements were taken at three time points (10, 30 and 60 minutes) and the range of salicylate concentrations used was expanded (0mM, 10 uM, 100 uM, 1mM and 10 mM) | #Miller assay (see [[Glasgow/Wetlab/Protocols#Protocol 10: Miller Assay|Protocol 10]]) repeated on ''E.coli'' cultures grown up in minimal media. Measurements were taken at three time points (10, 30 and 60 minutes) and the range of salicylate concentrations used was expanded (0mM, 10 uM, 100 uM, 1mM and 10 mM) | ||
- | |||
<br> | <br> | ||
- | |||
{| border="1" cellpadding="6" align="center" | {| border="1" cellpadding="6" align="center" | ||
- | |||
|- align="center" | |- align="center" | ||
!rowspan=2 | [Salicylate] (uM) | !rowspan=2 | [Salicylate] (uM) | ||
Line 446: | Line 458: | ||
|10000 || 0.481 || 0.485 || 0.484 | |10000 || 0.481 || 0.485 || 0.484 | ||
|} | |} | ||
- | |||
<br> | <br> | ||
- | |||
{| border="1" cellpadding="6" align="center" | {| border="1" cellpadding="6" align="center" | ||
|- align=center | |- align=center | ||
Line 487: | Line 497: | ||
|0 || 0.10 || 0.10 || 0.12 || 1005.9 || 1015.8 || 1147.9 || 0.23 || 0.23 || 0.23 || 752.0 || 752.8 || 732.8 || 0.42 || 0.42 || 0.42 || 683.6 || 695.3 || 687.4 | |0 || 0.10 || 0.10 || 0.12 || 1005.9 || 1015.8 || 1147.9 || 0.23 || 0.23 || 0.23 || 752.0 || 752.8 || 732.8 || 0.42 || 0.42 || 0.42 || 683.6 || 695.3 || 687.4 | ||
|- align=”center” | |- align=”center” | ||
- | | | + | |10 || 0.12 || 0.11 || 0.11 || 1133.7 || 1065.9 || 1085.7 || 0.24 || 0.24 || 0.24 || 768.7 || 768.7 || 749.2 || 0.45 || 0.45 || 0.46 || 726.6 || 723.5 || 715.9 |
|- align=”center” | |- align=”center” | ||
- | | | + | |100 || 0.12 || 0.12 || 0.12 || 1109.0 || 1115.3 || 1117.4 || 0.24 || 0.25 || 0.25 || 783.9 || 781.3 || 789.1 || 0.46 || 0.48 || 0.46 || 734.5 || 748.3 || 716.5 |
|- align=”center” | |- align=”center” | ||
- | | | + | |1000 || 0.12 || 0.12 || 0.11 || 1151.6 || 1155.3 || 1061.8 || 0.25 || 0.25 || 0.22 || 783.7 || 812.3 || 704.6 || 0.48 || 0.48 || 0.49 || 761.4 || 771.8 || 788.3 |
|- align=”center” | |- align=”center” | ||
- | | | + | |10000 || 0.12 || 0.12 || 0.12 || 1237.0 || 1216.5 || 1239.7 || 0.26 || 0.25 || 0.26 || 890.5 || 841.9 || 898.8 || 0.48 || 0.48 || 0.48 || 831.6 || 817.9 || 824.7 |
- | + | ||
|} | |} | ||
- | |||
<br> | <br> | ||
- | |||
#A 1% gel was run for the p1010 PCR products from 02/08. | #A 1% gel was run for the p1010 PCR products from 02/08. | ||
#*23N (pSB1AK3) plasmid size ~3800bp - AvaI did not cut the biobrick. | #*23N (pSB1AK3) plasmid size ~3800bp - AvaI did not cut the biobrick. | ||
#*20G (pSB1A2) plasmid size ~2700bp - digest worked! | #*20G (pSB1A2) plasmid size ~2700bp - digest worked! | ||
- | |||
<br> | <br> | ||
- | |||
{| border="1" cellspacing="0" cellpadding="5" align="center" | {| border="1" cellspacing="0" cellpadding="5" align="center" | ||
!Label | !Label | ||
Line 541: | Line 546: | ||
|2304bp, 1722bp | |2304bp, 1722bp | ||
|2304bp, 1722bp (but not in same digest) | |2304bp, 1722bp (but not in same digest) | ||
+ | |} | ||
+ | <br> | ||
+ | {| valign=top cellpadding=3 | ||
+ | |- | ||
+ | ![[Glasgow/Wetlab/Week4|<font face=georgia color=#3366CC size=4>Previous <br> Week</font>]] || [[Glasgow/Wetlab/Week6|<font face=georgia color=#3366CC size=4>Next <br> Week</font>]] | ||
+ | |- | ||
+ | |} | ||
+ | ---- | ||
+ | {| valign=top cellpadding=3 | ||
+ | |- | ||
+ | !align=center|[[Image:Uog.jpg]] || [[Glasgow|<font face=georgia color=#3366CC size=4>Back To <br> Glasgow's <br> Main Page</font>]] || [[Glasgow/Wetlab|<font face=georgia color=#3366CC size=4>Back To <br> Glasgow's <br> Wetlab Log</font>]] | ||
|} | |} |
Latest revision as of 15:32, 25 October 2007
Back To Glasgow's Main Page | Back To Glasgow's Wetlab Log | Go To Glasgow's Drylab Log |
---|
Protocols | References | Resources | Orders | Biobricks Used | Gels |
Contents[hide] |
Week 5
Monday 30th July 2007
-
Minipreps done (see Protocol 5):
Gene Label/Biobrick ID Primers Colonies Constructor 4/7A 1, 2, 3, 4, 5, 6, 7, 8, 9 Constructor 4/11C 1 Constructor 4/11C 10 – 13 did not grow overnight Constructor 2/23N 26, 27, 28, 32 Constructor 3/20G 29, 30, 31, 33, 34, 35 PhzM B1 1, 2 PhzS B3 1, 2, 3 PhzS Bbp_PhzS_for_1 and Bbs_Oxy_2 20, 21, 22 PhzM Bbp_PhzM_for_1 and Bbs_PhzM_rev_1 23, 24, 25 PhzS Bbp_Oxy_1 and Bbs_Oxy_2 14, 15, 16 PhzM Bbp_Methyl_1 and Bbs_Methyl_2 17, 18, 19 -
PCR to check if the BioBrick transformants contain the expected size inserts (used VF2 and VR primers) with Reddymix and Touch 2 program (see Protocol 9). Tested:
Label 4/11C 4/7A 4/5I 4/5O 4/6B 3/19A 1/9G 1/16P 1/5H B1 B3 B5 Colonies 10, 11, 12 5, 6, 7 1, 2, 3 1, 2 1, 2, 3 1, 2, 3, 4 1, 2, 3 1, 2, 3 1, 2, 3 17, 18, 19, 25, 26, 27 20, 21, 22, 23, 24 14, 15, 16, 28, 29 - Diluted new primers which arrived according to the labels.
- Ran new PCR testing the XylR, Pr and Pu primers (original and new which arrived 30/7/07) on mt-2 with Reddymix and Touch2. Both sets of primers successful. The pGLTUR stock was unreliable.
- PCR of the 7 gene operon with Reddymix, Touch 2 with an extension time of 8 mins and Pseudomonas Aeruginosa DNA as template. No desired bands seen. Primer combinations as follows:
- Bbp_PhzA_for and Bbs_PhzG_rev
- Bbp_PhzA_for and Bbs_PhzD_rev
- Bbp_PhzD_for and Bbs_PhzG_rev
- Restriction digest (see Protocol 7) of 3/20G and 2/23N. Used Promega's AvaI for both digests and buffer B, 1hr at 37°C. Ran 10ul of the reaction with 2ul of loading dye on a 1% agarose gel. No bands showed up on the gel picture.
Label BioBrick Description Colonies Expected Bands 3/20G [http://partsregistry.org/Part:BBa_P1010 Bba_p1010] in pSB1AC3 V1005 29, 30, 31, 33, 34, 35 1462bp, 1376bp, 892bp 2/23N [http://partsregistry.org/Part:BBa_P1010 Bba_p1010] in pSB1AK3 V1005 26, 27, 28, 32 1462bp, 1376bp, 569bp, 457bp - To understand why restriction digests did not appear, ran gel of miniprepped DNA. No bands present. Minipreps ran:
- 2/23N: Colonies 26, 27, 28
- 3/20G: Colonies 30, 31
- Cleaned out cells and reassembled according to NCBE protocol, using one as a negative control replacing yeast with water.
Tuesday 31st July 2007
- Cells reassembled because they had leaked over night.
- PCR (see Protocol 9) of the 7 gene operon repeated using KOD
-
polymerase and KOD program. Amplified A-D 3.5kb and D-G 3.5kb. Primer pair as follows:
- Bbp_PhzA_for and Bbs_PhzG_rev
- Bbp_PhzA_for and Bbs_PhzD_rev
- Bbp_PhzD_for and Bbs_PhzG_rev
-
PCR (see Protocol 9) of the 7 gene operon repeated using KOD XL polymerase and KOD XL program. Amplified A-G 7kb. Primer pair as follows:
- Bbp_PhzA_for and Bbs_PhzG_rev
- Bbp_PhzA_for and Bbs_PhzD_rev
- Bbp_PhzD_for and Bbs_PhzG_rev
-
Gel ran of yesterday's BioBrick confirmation (VF2 and VR) PCR. Expected sizes and results as follows:
Label 4/11C 4/7A 4/5I 4/5O 4/6B 3/19A 1/9G 1/16P 1/5H B1 B3 B5 Expected Sizes 981bp 4096bp 1396bp 1396bp 1396bp 273bp 293bp 535bp 958bp 1072bp 1262bp 1260bp Results Correct All wrong Correct Correct 2 and 3 correct Correct Correct Correct Correct 17, 18, 19, 26 correct 23 correct All wrong -
Restriction digests of constructors 2/23N and 3/20G carried out again using Roche enzymes (see Protocol 7), Buffer B and incubation for at least 1hr at 37°C. All bands on gel are between 2 and 2.5 kb. Digests as follows:
Constructor Colonies Enzymes Expected Sizes 2/23N in pSB1AK3 26, 27, 32 BamHI, XhoI 1046bp, 1026bp, 1792bp 3/20G in pSB1AC3 29, 30, 31, 33, 34, 35 BamHI, XhoI 1046bp, 892bp, 1792bp - Overnights set up to test resistances of the 2/23N and 3/20G constructors. All colonies 26-35 grown on carbenicillin LB, and colonies 31, 33 and 34 also grown in chloramphenicol LB.
Wednesday 1st August 2007
- Meeting with modellers about biobricks.
- Of yesterday's overnights, the 3 with chloramphenicol did not grow. This confirms that 3/20G is 3/20G and not 2/2B as previously believed as a result of mislabelling. All overnights then miniprepped according to Qiagen protocol.
- New restriction digest for new miniprepped 3/20G and 2/23N. 3/20G using Roche enzymes, Buffer B and incubating for at least 1hr at 37°C, digestion worked. 2/23N using Promega's AvaI restriction enzyme as on 30/7/07, AvaI cut the plasmid but not the biobrick.
- 3/20G in pSB1AC3, colonies 30 and 31: BamHI, PvuI – 1411bp, 1343bp (Xho does not cut).
- Overnights set up: 2/23N – 26, 27, 28 and 3/20G – 33 (all carb).
- Gel run of 7 gene operon PCR from 31/7/07 and DNA extracted according to Qiagen Gel Extraction Microcentrifuge Protocol (see Protocol 11).
- PCR (see Protocol 9) repeated for XylR, Pr and Pu because the previous Pu primer combinations did not work. Primer combinations as follows:
- XylR preffix and XylR suffix
- Pr prefix and Pr suffix
- Pr_for_2 and XylR_rev_2
- Pu_Pre_EM and Pu_Suf_AFT
- Pu_Pre_AFT and Pu_Suf_EM
- Researched restriction maps for plasmids with death genes.
- Overnights set up with the intention of digesting constructors of PhzM and PhzS after miniprepping in the morning, hopefully getting ligations that will transform TOP10 cells to grow overnight. Colonies were chosen that gave a positive result of the right predicted size (see 31/7/07) on a gel of PCR with VF2 and VR primers.
- 4/11C constructor – 10, 11, 12 (Kan)
- 4/5I constructor – 1, 2, 3 (Carb)
- 4/5O constructor – 1, 2, 3 (Kan)
- 4/6B constructor – 2, 3 (Kan)
- B1 PhzM - 17, 18, 19, 26 (Carb)
- B3 PhzS - 20 (Carb)
- C5 PhzM - 24, 25 (Carb)
- Miller Assay was performed (according to Protocol 10) on E. coli cell culture aliquots containing the DntR system grown up in LB. A range of salicylate concentrations (0 mM, 20 uM, 50 uM, 100 uM and 200 uM)were added to aliqouts and then allowed to grow for a further 3 hours. As this was a trial run, measurements at only one time point (58 minutes) were taken. The spectrophotometer readings and their corresponding calculated Miller units are shown in the table below.
[Salicylate] (uM) | Abs600 | Abs420 | Miller units | ||||||
---|---|---|---|---|---|---|---|---|---|
Rep A | Rep B | Rep C | Rep A | Rep B | Rep C | Rep A | Rep B | Rep C | |
0 | 0.386 | 0.480 | 0.495 | 0.209 | 0.257 | 0.317 | 466.8 | 461.6 | 552.1 |
20 | 0.676 | 0.814 | 0.473 | 0.431 | 0.450 | 0.364 | 549.6 | 476.6 | 663.4 |
50 | 0.494 | 0.495 | 0.476 | 0.380 | 0.396 | 0.489 | 663.1 | 689.7 | 885.6 |
100 | 0.533 | 0.464 | 0.507 | 0.373 | 0.357 | 0.463 | 603.3 | 663.3 | 787.3 |
200 | 0.551 | 0.529 | 0.521 | 0.526 | 0.548 | 0.451 | 823.0 | 893.0 | 746.2 |
The very high level of LacZ expression throughout the range of concentrations of salicylate could be due to the content of tryptophan in the LB media which could act upon the DntR responsive promoter. In order to try and minimize the background LacZ expression due to the presence of aromatic compounds present in the LB media, cell cultures will be grown up in minimal media instead.
Thursday 2nd August 2007
- Minimal media prepared for the Miller Assay because it does not interfere with enzyme activity (see Protocol 10).
- Minipreps (see Protocol 5) done of yesterday's overnights for PhzM and PhzS.
- Digestions (see Protocol 7) done of these PhzM and PhzS minipreps:
Gene | Label | Colonies | Primers | Enzyme | Orientation 1 | Orientation 2 | Results |
---|---|---|---|---|---|---|---|
PhzM | B1 | 17, 18, 19, 26 | PhzM_for_1 + Methyl_2 | PstI | 4243bp, 443bp, 275bp | 3683bp, 835bp, 443bp | 17, 18 + 26 possibly in orientation 1 |
PhzM | B1 | 17, 18, 19, 26 | PhzM_for_1 + Methyl_2 | EcoRI | 3654bp, 1287bp, 18bp | 4654bp, 286bp, 18bp | 17, 18 + 26 possibly in orientation 1 |
PhzM | C5 | 24, 25 | PhzM_for_1 + PhzM_rev_1 | PstI | 4243bp, 443bp, 275bp | 3683bp, 835bp, 443bp | Appears wrong |
PhzM | C5 | 24, 25 | PhzM_for_1 + PhzM_rev_1 | EcoRI | 4243bp, 443bp, 275bp | 3683bp, 835bp, 443bp | Possibly in orientation 1 |
PhzS | B3 | 20 | PhzS_for_1 + Oxy_2 | PstI | 4012bp, 534bp, 344bp, 275bp | 3683bp, 604bp, 534bp, 344bp | Possibly in orientation 1 |
PhzS | B3 | 20 | PhzS_for_1 + Oxy_2 | EcoI | 3656bp, 1491bp, 18bp | 4682bp, 285bp, 18bp | Possibly in orientation 1 |
- PCR (see Protocol 9) done with newly arrived death gene primers on the miniprepped DNA to make sure the BioBrick overnights genuinely carry their respective versions of ccdB (esp 23N as it does not run correctly on the gel) using Reddymix and Touch 2 with Tm of 60C and 28 cycles, saved as PCR60DEG.
Reference | Colonies |
---|---|
4/11C | 10, 11, 12 |
4/5I | 1, 2, 3 |
4/6B | 2, 3 |
4/5O | 1, 2, 3 |
2/23N | 26, 27, 33 |
3/20G | 28 |
- PCR (see Protocol 9) also done (using the primers used to create the cloned versions of PhzM and PhzS) on minipreps, done this morning, of TOPO cloning (hopefully containing PhzM and PhzS) to confirm that the insert is genuinely there. Used Reddymix and Touch2. All constructs appear to contain the correct genes.
Gene | Label | Colonies | Primers | Size | Results |
---|---|---|---|---|---|
PhzM | B1 | 17, 18, 19, 26 | PhzM_for_1 + Bbs_Methyl_2 | 1072bp | Appears correct |
PhzS | B3 | 20 | PhzS_for_1 + Oxy_2 | 1220bp | Appears correct |
PhzM | C5 | 24, 25 | PhzM_for_1 + PhzM_rev_1 | 1225bp | 24 possibly too big, 25 appears wrong |
Friday 3rd August 2007
- Miller assay (see Protocol 10) repeated on E.coli cultures grown up in minimal media. Measurements were taken at three time points (10, 30 and 60 minutes) and the range of salicylate concentrations used was expanded (0mM, 10 uM, 100 uM, 1mM and 10 mM)
[Salicylate] (uM) | Abs600 | ||
---|---|---|---|
Rep A | Rep B | Rep C | |
0 | 0.512 | 0.507 | 0.514 |
10 | 0.516 | 0.516 | 0.525 |
100 | 0.523 | 0.529 | 0.528 |
1000 | 0.521 | 0.515 | 0.518 |
10000 | 0.481 | 0.485 | 0.484 |
Time after addition of substrate solution | ||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
10 minutes | 30 minutes | 60 minutes | ||||||||||||||||
[Salicylate] (uM) | Abs420 | Miller units | Abs420 | Miller units | Abs420 | Miller units | ||||||||||||
Rep A | Rep B | Rep C | Rep A | Rep B | Rep C | Rep A | Rep B | Rep C | Rep A | Rep B | Rep C | Rep A | Rep B | Rep C | Rep A | Rep B | Rep C | |
0 | 0.10 | 0.10 | 0.12 | 1005.9 | 1015.8 | 1147.9 | 0.23 | 0.23 | 0.23 | 752.0 | 752.8 | 732.8 | 0.42 | 0.42 | 0.42 | 683.6 | 695.3 | 687.4 |
10 | 0.12 | 0.11 | 0.11 | 1133.7 | 1065.9 | 1085.7 | 0.24 | 0.24 | 0.24 | 768.7 | 768.7 | 749.2 | 0.45 | 0.45 | 0.46 | 726.6 | 723.5 | 715.9 |
100 | 0.12 | 0.12 | 0.12 | 1109.0 | 1115.3 | 1117.4 | 0.24 | 0.25 | 0.25 | 783.9 | 781.3 | 789.1 | 0.46 | 0.48 | 0.46 | 734.5 | 748.3 | 716.5 |
1000 | 0.12 | 0.12 | 0.11 | 1151.6 | 1155.3 | 1061.8 | 0.25 | 0.25 | 0.22 | 783.7 | 812.3 | 704.6 | 0.48 | 0.48 | 0.49 | 761.4 | 771.8 | 788.3 |
10000 | 0.12 | 0.12 | 0.12 | 1237.0 | 1216.5 | 1239.7 | 0.26 | 0.25 | 0.26 | 890.5 | 841.9 | 898.8 | 0.48 | 0.48 | 0.48 | 831.6 | 817.9 | 824.7 |
- A 1% gel was run for the p1010 PCR products from 02/08.
- 23N (pSB1AK3) plasmid size ~3800bp - AvaI did not cut the biobrick.
- 20G (pSB1A2) plasmid size ~2700bp - digest worked!
Label | BioBrick ID | Enzyme | Expected Bands | Bands Seen |
---|---|---|---|---|
4/11C | p1010 pSB3K3 | AvaI | 4419bp, 604bp, 569bp, 274bp | 604bp |
4/5O | IS2001 pSB4K5 | AvaI, SspI | 2044bp, 1546bp, 594bp, 307bp, 18bp | 2044bp, 1546bp, 594bp, 307bp |
4/6B | IS2001 pSB3K5 | AvaI, SspI | 3153bp, 568bp, 307bp | 3151bp, 568bp, 307bp |
4/5I | IS2001 pSB4A5 | AvaI, SspI | 1605bp, 1572bp, 987bp, 307bp, 14bp | 1605bp, 1572bp, 307bp |
4/6B | IS2001 pSB3K5 | AvaI, NheI | 2304bp, 1722bp | 2304bp, 1722bp (but not in same digest) |
Previous Week | Next Week |
---|
Back To Glasgow's Main Page | Back To Glasgow's Wetlab Log |
---|