Team:Bielefeld-Germany/Labjournal/week21

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Latest revision as of 21:32, 25 September 2012

==Week 21 (09/17 - 09/23/12)==

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 ==Week 21 (09/17 - 09/23/12)==
-===Monday September 17th===
-* '''Team Cultivation & Purification:'''
-** Cell disruption of fermentation of ''E.&nbsp;coli'' Rosetta-Gami 2 with [http://partsregistry.org/wiki/index.php?title=Part:BBa_K863012 BBa_K863012] via high-pressure homogenization and purification via Ni-NTA column.
-[[File:Bielefeld2012 420ColiMeOH.jpg|thumb|left|Activity of [http://partsregistry.org/Part:BBa_K863005 ECOL] measured via oxidized ABTS at OD<sub>420</sub> in relation to a MeOH gradient.]]
-[[File:Bielefeld2012 530ColiMeOH.jpg|thumb|right|Activity of [http://partsregistry.org/Part:BBa_K863005 ECOL] measured via oxidized ABTS at OD<sub>530</sub> in relation to a MeOH gradient.]]
-* '''Team Activity Tests:'''
-** Another day full of measurements is over! Today we measured some more samples from Team Immobilization: check their labjournal. As well we went on with characterizing our laccases. [http://partsregistry.org/Part:BBa_K863005 ECOL] was analyzed regarding its behavior in different concentrations of MeOH and acetonitrile. The activity was measured with concentrations of 2-16 µL, respectively. Since ABTS is changing it´s emission spectrum when being in contact with methanol we also detected the OD<sub>530</sub>. As expected ECOL is happier when only little MeOH is in its environment. We did the same measurements with acetonitrile and got the same result: the fewer acetonitrile, the better for ECOL. Again, we will hand over these results to Team Substrate Analytics.
-[[File:Bielefeld2012 420ColiAceto.jpg|thumb|left|Activity of [http://partsregistry.org/Part:BBa_K863005 ECOL] measured via oxidized ABTS at OD<sub>420</sub> in relation to a acetonitrile gradient.]]
-[[File:Bielefeld2012 530ColiAceto.jpg|thumb|right|Activity of [http://partsregistry.org/Part:BBa_K863005 ECOL] measured via oxidized ABTS at OD<sub>530</sub>in relation to a acetonitrile gradient.]]
-===Tuesday September 18th===
-* '''Team Cellulose Binding Domain:'''
-** Primer arrived:
-** Gradient-PCR with the [http://partsregistry.org/Part:BBa_K863103 CBDcex(T7)+GFP_His]-plasmid and S3N10-CBDcex_RV and S3N10-GFP_FW primer-mix. the right product appeared only at 66,5°C; Lower: wrong product; Higher: no product
-*** Following PCR at 66,5°C(50µL) had the wrong product (main product at 2 kbp); could be because of a different template concentration or not exact temperature.
-*** Alternativly took the 20 µL-tube with right product and added 0,5 µL ''Dpn''I for over-night digestion.
-** Gradient-PCR with [http://partsregistry.org/Part:BBa_K863103 CBDcex(T7)+GFP_His]-template and a CBDcex_Freiburg- + GFP_Freiburg_compl-primer-mix to amplify the whole fusion-protein and get rid of the His-tag.
-** Gradient-PCR with [http://partsregistry.org/Part:BBa_K863113 CBDclos(T7)+GFP_His]-template and a CBDclos_Freiburg- + GFP_Freiburg_compl-primer-mix to amplify the whole fusion-protein and get rid of the His-tag.
-* '''Team Activity Tests:'''
-[[File:Bielefeld2012 Colicoppergradient.jpg|thumb|right|Fig. 1: Measurements of [http://partsregistry.org/Part:BBa_K863005 ECOL] in a CuCl gradient of 0,1 to 0,7 mM. The activity was measured via oxidized ABTS at OD<sub>420</sub>, (n=4).]]
-** Today we measured the activity of our [http://partsregistry.org/Part:BBa_K863005 ECOL] laccase in a CuCl gradient to check whether another concentration than the one we usually incubated the laccases with might be more optimal. We chose a gradient from 0,1 mM to 0,7 mM (with an increment of 0,1) and measured the incubated samples as usual in 100 mM sodium acetate buffer, 0,1 mM ABTS (ad 200 µL H<sub>2</sub>O), respectively. Fig. 1 shows that the chosen concentration do influence ECOL, 0,4 mM seems like the best choice for incubation before the activity measurments. Thus the spectrum of OD<sub>420</sub> maxima is not immensely wide so that [http://partsregistry.org/Part:BBa_K863005 ECOL] seems to be satisfied with any CuCl concentration.
-[[File:Thermo180912.jpg|thumb|right|Fig. 2: Activity measurements of [http://partsregistry.org/wiki/index.php/Part:BBa_K863010 TTHL] via OD<sub>420</sub>.]]
-** Additionally we measured the activity of [http://partsregistry.org/wiki/index.php/Part:BBa_K863010 TTHL] at 25°C and in sodium acetate buffer (pH 5). TTHL finally also shows some activity, our favorite fractions of Team Cultivations output are number 1 and 2. Unfortunately TTHL couldn´t be indentified correctly via [https://2012.igem.org/Team:Bielefeld-Germany/Protocols/Analytics#MALDI MALDI] yet so that we will have to wait with further characterizing until we get the go through the MALDI results.
-* '''Team Substrate Anayltics''':
-** We analyze Ethin estradiol and estradiol degradation with the Spectrofluorophotometer. The measure showed that the degradation product are detectable but the results weren't clear. We decide to do this measurement again to have better results so a new degradation of the two substrates were set.
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-===Wednesday September 19th===
-* '''Team Cellulose Binding Domain:'''
-** Stopped over-night-''Dpn''I-digestion of S3N10-clos-GFP_his PCR-product and cleaned up in gel. Ligated the PCR-product with itself via Blunt-end-ligation and transformed it into KRX. Plated on Select-Agar.
-** Gradient-PCRs of the [http://partsregistry.org/Part:BBa_K863103 CBDcex(T7)+GFP_His]-plasmid and a [http://partsregistry.org/Part:BBa_K863113 CBDclos(T7)+GFP_His]-plasmid (unsequenced) with the CBDcex_Freiburg- and GFP_Freiburg-compl- and the CBDclos_Freiburg- and GFP_Freiburg_compl primers, respectively. The CBDcex-setup showed no correct product, but the CBDclos-setup had the right bands at temperatures from 57°C to 64°C; Merged the correct fractions and cleaned them up through the gel.
-**Digested the cleaned-up product with ''Spe''I and ''Xba''I and ''Dpn''I.
-**Ligated <partinfo>J61101</partinfo> and [http://partsregistry.org/Part:BBa_K863111 CBDclos_Freiburg] with [http://partsregistry.org/Part:BBa_K863120 GFP_Freiburg] and transformed it into KRX.
-* '''Team Activity Test''':
-** What a day! The deadline is coming closer and we still had (!) a lot of measurements to do, so today was chosen to be a day full of important measurements. First we measured the activity of the TVEL0 and [http://partsregistry.org/wiki/index.php/Part:BBa_K863000 BPUL] in a CuCl gradient. As well we examined what our [http://partsregistry.org/wiki/index.php/Part:BBa_K863000 BPUL] laccase does when its supposed to work in different pHs. [http://partsregistry.org/wiki/index.php/Part:BBa_K863000 BPUL] was additionally characterized regarding its behavior in different concentrations of MeOH and acetonitrile. This output is of course most interesting for Team Substrate Analytics. [[File:Bielefeld2012 ColiNaAcBRP.jpg|thumb|right|Comparison of activity of [http://partsregistry.org/Part:BBa_K863005 ECOL] in sodium acetate buffer and Britton-Robinson buffer, measured at OD<sub>420</sub> respectively.]]Since we already compared the behaviour of TVEL0 in the environment of sodium acetate buffer (pH 5) and Britton-Robinson buffer (pH 5), respectively, we also compared [http://partsregistry.org/wiki/index.php/Part:BBa_K863000 BPUL] and [http://partsregistry.org/Part:BBa_K863005 ECOL] in those buffers. ECOL is not impressed by the two different buffer systems and thus not influenced in it´s activity.
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-===Thursday September 20th===
-* '''Team Fungal and Plant Laccases :'''
-** Our primers for GFP, tvel35, tvel5 and <partinfo>BBa_K500002</partinfo> arrived. We did PCR on GFP with the new primers for cloning in our shuttle vector.
-* '''Team Cellulose Binding Domain:'''
-**No Colonies on the S3N10-[http://partsregistry.org/Part:BBa_K863113 CBDclos(T7)+GFP_His]-transformations-dish with the blunt-end ligation; reason: forgotten to phosphorylate the PCR-product.
-** Two colonies on the CBDclos+GFP-dish with the constitutive [http://partsregistry.org/Part:BBa_J61101 J23100 + J61101] promoter. But none of them is glowing. And them shouldn't ... used the wrong selection-agar (since J61101 carries pSB1A2-backbone with AMP-resistence.
-* '''Team Activity Tests:'''
-[[File:Bielefeld2012 10und25Grad.jpg|thumb|right|Temperatur measurements of [http://partsregistry.org/Part:BBa_K863005 ECOL] at 10°C and 25°C. Measurements were done via optical density 420 nm.]]
-** Today we started another exciting measurement. Today was all about temperatures. Through our cooperation with the clarification plant we found out that the waster water here in Germany has a minimal temperature of 10°C throughout the year. We used this value together with our previous measurements at 25°C to complete the temperature gradient of our measurements. Eventhough [http://partsregistry.org/Part:BBa_K863005 ECOL]  shows an increased activity at 10°C, it does reach a comparable OD value as the samples measured at 25°C. The increased activity is expressed by achieving the maximal OD<sub>420</sub> slower than the laccase measured at 25°C. This seems like good news for Team Modeling.
-* '''Team Substrate Analytics''':
-** Degradation measure from Ethin estradiol and Estradiol with the Spectrofluorophotometer. Degradation was from the [https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week21#Tuesday_September_18th 18th September]
-===Friday September 21st===
-* '''Team Cellulose Binding Domain:'''
-** Transformated <partinfo>J61101</partinfo> with CBDclos+GFP again and plated on the right selection-agar this time!
-[[File:Bielefeld2012 ColiABTSGradient.jpg|thumb|right|[http://partsregistry.org/Part:BBa_K863005 ECOL] activity with different concentration of ABTS.]]
-* '''Team Activity Tests:'''
-** Another part of the characterization of our [http://partsregistry.org/Part:BBa_K863005 ECOL] and [http://partsregistry.org/wiki/index.php/Part:BBa_K863000 BPUL] laccase was to measure their activity when exposed to different concentrations of ABTS. We choose an exponential gradient of 2 µL to 16 µL and measured with the usual laccase concentration of 0,003 mg/mL and 100 mM sodium acetate buffer (ad 200 µL H<sub>2</sub>O). Unfortunately the measurements that contained 16 µL ABTS could not be measured completely because the OD<sub>420</sub> exceeded the maximal value that [https://2012.igem.org/Team:Bielefeld-Germany/Protocols/Materials#Tecan_Infinite_Microplate_Reader Tecan] was able to measure. The results of [http://partsregistry.org/Part:BBa_K863005 ECOL] (see. Fig. 1) show as well an exponential increase in the OD<sub>420</sub> correlated to the ABTS concentrations, respectively. The negative control was chosen to contain the maximum of 16 µL ABTS in buffer and water that was incubated with CuCl.
-===Saturday September 22nd===
-* '''Team Fungal Laccases:'''
-*Digest of  <partinfo>BBa_K863204</partinfo> for cloning GFP in the vector and to show that the vector is working.
-* '''Team Cellulose Binding Domain:'''
-** Once again two colonies on the agar-dish: can not say if they have a green glow...
-*** picked the colonies and them put into AMP-LB-Medium.
-** Also made a flask with 10 mL LB-Medium and cells with the [http://partsregistry.org/Part:BBa_K863104 CBDcex(J61101)+GFP_His]-plasmid
-* '''Team Cultivation & Purification:'''
-** For collaboration with [https://2012.igem.org/Team:University_College_London UCL London]: Made precultures of ''E. coli'' KRX with <partinfo>BBa_K729006</partinfo>, with <partinfo>BBa_K863005</partinfo> and without plasmid.
-===Sunday September 23rd===
-* '''Team Cellulose Binding Domain:'''
-** All cultures did not show any sign of GFP-glow under uv-light.
-** Gradient-PCR of <partinfo>BBa_K863104</partinfo> with S3N10_Cex_compl- and S3N10_GFP-primermix to generate a 13 amino acid-linker between the cellulose binding domain and the GFP.
-** Transformated [http://partsregistry.org/Part:BBa_K863103 CBDcex(T7)+GFP_His] and [http://partsregistry.org/Part:BBa_K863113 CBDclos(T7)+GFP_His] into BL21, to test if the problem is in the expression-system.
-* '''Team Cultivation & Purification:'''
-[[File:Bielefeld2012_Wachstumskinetik_pLondon.jpg|200px|thumb|right|Figure x: Growth kinetics of flask cultivation of ''E. coli'' KRX with <partinfo>BBa_K729006</partinfo> and without plasmid as negative control using [https://2012.igem.org/Team:Bielefeld-Germany/Protocols/Materials#LB_medium LB-medium] and of ''E. coli'' KRX with <partinfo>BBa_K863005</partinfo> using [https://2012.igem.org/Team:Bielefeld-Germany/Protocols/Materials#Autoinduction_medium autoinduction medium]. Further parameters: final volume of 60&nbsp;mL, 60&nbsp;µg/mL chloramphenicol, 37&nbsp;°C, durance: 12&nbsp;hours.]]
-** For collaboration with [https://2012.igem.org/Team:University_College_London UCL London]: Cultivation of ''E. coli'' KRX with <partinfo>BBa_K729006</partinfo> and ''E. coli'' KRX without plasmid as negative control
-*** Settings: 250&nbsp;mL flasks without baffles, final volume: 60&nbsp;mL, [https://2012.igem.org/Team:Bielefeld-Germany/Protocols/Materials#LB_medium LB-medium], 60&nbsp;µg/mL chloramphenicol, 37&nbsp;°C, durance: 12&nbsp;hours.
-*** We determined the OD<sub>600</sub> for a growth kinetics (see figure X).
-** Cultivation of ''E. coli'' KRX with <partinfo>BBa_K863005</partinfo> for comparison.
-*** Settings: 250&nbsp;mL flasks without baffles, final volume: 60&nbsp;mL, [https://2012.igem.org/Team:Bielefeld-Germany/Protocols/Materials#Autoinduction_medium autoinduction medium], 60&nbsp;µg/mL chloramphenicol, 37&nbsp;°C, durance: 12&nbsp;hours.