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Latest revision as of 23:53, 26 October 2012

Parts for a reliable and field ready biosensing platform

Implementation of biosensors in real world situations has been made difficult by the unpredictable and non-quantified outputs of existing solutions, as well as a lack of appropriate storage, distribution and utilization systems. This leaves a large gap between a simple, functional sensing mechanism and a fully realised product that can be used in the field. We aim to bridge this gap at all points by developing a standardised ratiometric luciferase output in a Bacillus chassis. This output can be linked up with prototyped instrumentation and software for obtaining reliable quantified results. Additionally, we have reduced the specialized requirements for the storage and distribution of our bacteria by using Bacillus' sporulation system. To improve the performance of our biosensing platform we have genetically modified Bacillus’ germination speed. Lastly, we demonstrated the robustness of our system by testing it with a new fluoride riboswitch, providing the opportunity to tackle real life problems.

One minute tour! :)

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Judging Form

Please help the judges by filling out this form. Tell them what medal you think you deserve and why. Tell them which special prizes you should win. Help them find your best parts. Show them how you thought about the safety of your project. Helping the judges will help you too.

Team: Cambridge
Region: Europe
iGEM Year:2012
Track:Foundational Advance
Project Name:Parts for a reliable and field ready biosensing platform
Project Abstract: Implementation of biosensors in real world situations has been made difficult by the unpredictable and non-quantified outputs of existing solutions, as well as a lack of appropriate storage, distribution and utilization systems. This leaves a large gap between a simple, functional sensing mechanism and a fully realised product that can be used in the field.

We aim to bridge this gap at all points by developing a standardised ratiometric luciferase output in a Bacillus chassis. This output can be linked up with prototyped instrumentation and software for obtaining reliable quantified results. Additionally, we have reduced the specialized requirements for the storage and distribution of our bacteria by using Bacillus' sporulation system. To improve the performance of our biosensing platform we have genetically modified Bacillus’ germination speed. Lastly, we demonstrated the robustness of our system by testing it with a new fluoride riboswitch, providing the opportunity to tackle real life problems.

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iGEM Medals for non-software teams

We believe our team deserves the following medal:
- Bronze
- Silver
- √Gold

Because we met the following criteria (check all that apply and provide details where needed)

Requirements for a Bronze Medal

√Register the team, have a great summer, and plan to have fun at the Regional Jamboree.
√Successfully complete and submit this iGEM 2012 Judging form.
√Create and share a Description of the team's project using the iGEM wiki and the team's parts using the Registry of Standard Biological Parts.
√Plan to present a Poster and Talk at the iGEM Jamboree.
√Enter information detailing at least one new standard BioBrick Part or Device in the Registry of Standard Biological Parts. Including:
- √Primary nucleaic acid sequence
- √Description of function
- √Authorship
- Safety notes, if relevant.
- √Acknowedgment of sources and references
√Submit DNA for at least one new BioBrick Part or Device to the Registry.

Additional Requirements for a Silver Medal

√Demonstrate that at least one new BioBrick Part or Device of your own design and construction works as expected; characterize the operation of your new part/device.
√Enter this information and other documentation on the part's 'Main Page' section of the Registry
Part Number(s): [http://partsregistry.org/Part:BBa_K911004 BBa_K911004]

Additional Requirements for a Gold Medal: (one OR more)

Improve an existing BioBrick Part or Device and enter this information back on the Experience Page of the Registry.
Part Number(s): None
√Help another iGEM team by, for example, characterizing a part, debugging a construct, or modeling or simulating their system.
Link to this information on your wiki. Page name: Team:Cambridge/Outreach/Collaboration
√Outline and detail a new approach to an issue of Human Practice in synthetic biology as it relates to your project, such as safety, security, ethics, or ownership, sharing, and innovation.
Link to this information on your wiki.
Page name: Team:Cambridge/HumanPractices/Overview,Team:Cambridge/HumanPractices/MarketResearch,Team:Cambridge/HumanPractices/FutureDirections

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iGEM Prizes

All teams are eligible for special prizes at the Jamborees. more... To help the judges, please indicate if you feel you should be evaluated for any of the following special prizes:

√Best Human Practice Advance
√Best Experimental Measurement
Best Model

Please explain briefly why you should receive any of these special prizes:

Best Human Practice Advance:

We feel that we deserve this prize for three reasons:

We explored the impacts, *both positive and negative*, of synthetic biology as a solution to real world problems, through interviewing professionals working in a relevant field, namely the impact of arsenic water contamination in Bangladesh.
We recognized existing problems with the way the current direction of synthetic. On going through the registry we found that most of the characterization data for biosensing parts is often neither comparable nor replicable. We have worked to solve this issue, for example with our ratiometric dual channel output.
*Our project doesn’t stop here*, in Chanel number 6 (Team:Cambridge/HumanPractices/FutureDirections) we considered the future implications and technological applications of our project, as well as the means by which it could be improved by subsequent users. We feel that the end to an iGEM project should not be the conclusion of an idea, but the start of it.

Best BioBrick Measurement Approach:

It is absolutely vital that a quantitative, numerical, robust, and flexible measurement approach exists to relay information to a user that is an accurate representation of the input processed by a biological device. Working from these principles, the following was done:

We designed and built Biologger, a *cheap, arduino-based, fully functional automatic rotary device* that has an incorporated ratiolumnometer
Our project is entirely open-sourced and open-platform. We have published source code for the two applications which serve to operate the device, one for PCs and the other for Android devices, as well as the open source circuit design that provides this ratiometric reading. Furthermore, the Android app is able to receive its data wirelessly, which we feel is a great advance in BioBrick measurement.
Our dual-channel luciferase reporter was successfully tested with a dilution series of E.coli transformed with the Lux Operon (under pBAD) biobrick (Part BBa_K325909) of the Cambridge iGEM 2010 team. It can detect, with good accuracy, both different light intensities, as well as the percentages of blue or orange frequencies in a sample.
Our device was successfully tested using artificial light to detect different frequencies (colours) as well.

Having done all the above, we believe that this fully open-sourced instrumentation kit (mechanical) chassis, electronics, software code), estimated at *$35.00* (or $85.00 if a Bluetooth modem is required), is a complete BioBrick measurement solution for any and all BioBricks with a light output.

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Team_Parts

To help the judges evaluate your parts, please identify 3 of your parts that you feel are best documented and are of the highest quality.

Best new BioBrick part (natural)
[http://partsregistry.org/Part:BBa_K911003 BBa_K911003]
Best new BioBrick part (engineered)
[http://partsregistry.org/Part:BBa_K911004 BBa_K911004]
Best improved part(s): None

List any other parts you would like the judges to examine:[http://partsregistry.org/Part:BBa_K911001 BBa_K911001], [http://partsregistry.org/Part:BBa_K911008 BBa_K911009], [http://partsregistry.org/Part:BBa_K911008 BBa_K911008]

Please explain briefly why the judges should examine these other parts:

Magnesium Sensitive Riboswitch [http://partsregistry.org/Part:BBa_K911001 BBa_K911001]
As a riboswitch sensing construct, this part is an entirely new type of biosensor (along with the fluoride construct) that could potentially change the way we think about designing input genetic circuits. Unlike the fluoride riboswitch, it is a derepression system and therefore serves to demonstrate the principle that riboswitches can be used regardless of whether they turn on or off their reporter.
Fluorescent ratiometric construct for standardizing promoter output [http://partsregistry.org/Part:BBa_K911009 BBa_K911009]
Fluorescence is a major cornerstone for biosensors in the registry, however, most parts do not involve the use of a ratiometric output, which has been shown in the literature to provide much more reliable and meaningful data. This part not only furthers the development of ratiometric measurements in molecular biology but due to the choice of promoters and terminators it can be used to characterize the difference in activity between E. coli and B. Subtilis
Fast Germination (B. subtilis) [http://partsregistry.org/Part:BBa_K911008 BBa_K911008]
This part is entirely novel for the registry and fully utilizes the recombination machinery inherent in the Bacillus chassis. Have spores that can germinate at a faster rate is certainly a worthy achievement and could help with experiments with B. Subtilis that any future iGEM teams may wish to perform.

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iGEM Safety

For iGEM 2012 teams are asked to detail how they approached any issues of biological safety associated with their projects.

The iGEM judges expect that you have answered the four safety questions Safety page on your iGEM 2012 wiki.

Please provide the link to that page: Page name: Team:Cambridge/Safety

Attribution and Contributions

For iGEM 2012 the description of each project must clearly attribute work done by the team and distinguish it from work done by others, including the host labs, advisors, and instructors.

Please provide the link to that page, or comments in the box below: Page name: Team:Cambridge/Attributions

Comments

If there is any other information about your project you would like to highlight for the judges, please provide a link to your wiki page here: Team:Cambridge/Overview/DesignProcess

MiniPrep

A method used to extract DNA from bacterial cells.

Theory

The miniprep kit relies on a column, which fits into a microcentrifuge tube which has alterable affinity for DNA depending on buffer which is washing through.

First centrifugation causes the cells to form a pellet at the bottom of the tube, this allows the medium in which the bacteria have been growing to be removed (the supernatant) and the cells can then be resuspended in another solution. This prinicple is used in many protocols to allow the solution surrounding the cell replaced with various buffers in the kit.

Bacterial cells are lysed by exposing them to a detergent (SDS) which solubilises the cell membrane, whilst sodium hydroxide disrupts the cell wall and more importnantly denatures the genomic DNA, the plasmid DNA and the proteins. The lysate is neutralized and adjusted to high salt concentration which causes denatured proteins, chromosomal DNA, cellular debris, and SDS to precipitate, while the smaller plasmid DNA renatures correctly and stays in solution. The chromosomal DNA is separated from the plasmid DNA because the chromsomal DNA binds to the QIAGEN membrane in the column along with the precipitating proteins and debris, whilst the plasmid DNA stays in solution and can be removed in the supernatant.

Growing up cell cultures for miniprep

Clean the lab bench by wiping down with 70% ethanol and paper towels.
Remove the agar plates for Part A and Part B from the incubator or 4°C fridge.
Label one 14ml culture tube for each Part. Add 5ml of LB broth (Amp/Kan) to each culture tube.
Use an inoculating loop to pick a single colony from each agar plate and inoculate the LB broth, in the appropriately labeled culture tube. Do not use the same inoculating loop more than once! Press lightly on the snap caps of the 14ml tubes, the caps should be a bit loose to allow for air flow.
Incubate for 16 hours at 37°C, in a rotator or shaker. Rotation helps the cells grow faster, and prevents them from settling at the bottom.
After incubation, the cell culture should be cloudy. You can now firmly press down on the snap caps to seal the tubes and store the cell culture at 4°C until you're ready to move onto the next step.

Preparation

Before using this protocol centrifuge 30ml cultured bactiera at 3000rpm for 15 minutes.

Practice

Used QIAprep Spin Mini Prep Kit, the protocol is adapted from the QIAprep Mini Prep Handbook [http://www.qiagen.com/hb/qiaprepminiprep QIAprep Mini Prep Handbook].

Resuspend pelleted bacterial cells in 250 μl Buffer P1 and transfer to a microcentrifuge tube. Ensure that RNase A has been added to Buffer P1. No cell clumps should be visible after resuspension of the pellet. If LyseBlue reagent has been added to Buffer P1, vigorously shake the buffer bottle to ensure LyseBlue particles are completely dissolved. The bacteria should be resuspended completely by vortexing or pipetting up and down until no cell clumps remain.
Add 250 μl Buffer P2 and mix thoroughly by inverting the tube 4–6 times. Mix gently by inverting the tube. Do not vortex, as this will result in shearing of genomic DNA. If necessary, continue inverting the tube until the solution becomes viscous and slightly clear. Do not allow the lysis reaction to proceed for more than 5 min.
Add 350 μl Buffer N3 and mix immediately and thoroughly by inverting the tube 4–6 times. To avoid localized precipitation, mix the solution thoroughly, immediately after addition of Buffer N3. Large culture volumes (e.g. ≥5 ml) may require inverting up to 10 times. The solution should become cloudy.
Centrifuge for 10 min at 13,000 rpm (~17,900 x g) in a table-top microcentrifuge. A compact white pellet will form.
Apply the supernatants from step 4 to the QIAprep spin column by decanting or pipetting.
Centrifuge for 30–60 s. Discard the flow-through.
Recommended: Wash the QIAprep spin column by adding 0.5 ml Buffer PB and centrifuging for 30–60 s. Discard the flow-through.This step is necessary to remove trace nuclease activity when using endA+ strains such as the JM series, HB101 and its derivatives, or any wild-type strain, which have high levels of nuclease activity or high carbohydrate content. Host strains such as XL-1 Blue and DH5αTM do not require this additional wash step.
Wash QIAprep spin column by adding 0.75 ml Buffer PE and centrifuging for 30–60s.
Discard the flow-through, and centrifuge for an additional 1 min to remove residual wash buffer. Important: Residual wash buffer will not be completely removed unless the flow-through is discarded before this additional centrifugation. Residual ethanol from Buffer PE may inhibit subsequent enzymatic reactions.
Place the QIAprep column in a clean 1.5 ml microcentrifuge tube. To elute DNA, add 50 μl Buffer EB (10 mM Tris·Cl, pH 8.5) or water to the center of each QIAprep spin column, let stand for 1 min, and centrifuge for 1 min.

Risk Assessment Back to Protocols

@@ Line 1: / Line 1: @@
-{{Template:Team:Cambridge/CAM_2012_TEMPLATE_HEAD_DIARY}}
+{{Template:Team:Cambridge/CAM_2012_TEMPLATE_HEADNEW}}
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 ==MiniPrep==
@@ Line 13: / Line 19: @@
 The lysate is neutralized and adjusted to high salt concentration which causes denatured proteins, chromosomal DNA, cellular debris, and SDS to precipitate, while the smaller plasmid DNA renatures correctly and stays in solution.
 The chromosomal DNA is separated from the plasmid DNA because the chromsomal DNA binds to the QIAGEN membrane in the column along with the precipitating proteins and debris, whilst the plasmid DNA stays in solution and can be removed in the supernatant.
+===Growing up cell cultures for miniprep===
+#Clean the lab bench by wiping down with 70% ethanol and paper towels.
+#Remove the agar plates for Part A and Part B from the incubator or 4°C fridge.
+#Label one 14ml culture tube for each Part. Add 5ml of LB broth (Amp/Kan) to each culture tube.
+#Use an inoculating loop to pick a single colony from each agar plate and inoculate the LB broth, in the appropriately labeled culture tube. Do not use the same inoculating loop more than once! Press lightly on the snap caps of the 14ml tubes, the caps should be a bit loose to allow for air flow.
+#Incubate for 16 hours at 37°C, in a rotator or shaker. Rotation helps the cells grow faster, and prevents them from settling at the bottom.
+#After incubation, the cell culture should be cloudy. You can now firmly press down on the snap caps to seal the tubes and store the cell culture at 4°C until you're ready to move onto the next step.
 ===Preparation===
@@ Line 22: / Line 36: @@
 [http://www.qiagen.com/hb/qiaprepminiprep QIAprep Mini Prep Handbook].
-;Step 1
-:Resuspend pelleted bacterial cells in 250 μl Buffer P1 and transfer to a microcentrifuge tube. Ensure that RNase A has been added to Buffer P1. No cell clumps should be visible after resuspension of the pellet. If LyseBlue reagent has been added to Buffer P1, vigorously shake the buffer bottle to ensure LyseBlue particles are completely dissolved. The bacteria should be resuspended completely by vortexing or pipetting up and down until no cell clumps remain.
-;Step 2
-:Add 250 μl Buffer P2 and mix thoroughly by inverting the tube 4–6 times. Mix gently by inverting the tube. Do not vortex, as this will result in shearing of genomic DNA. If necessary, continue inverting the tube until the solution becomes viscous and slightly clear. Do not allow the lysis reaction to proceed for more than 5 min.
-;Step 3
-:Add 350 μl Buffer N3 and mix immediately and thoroughly by inverting the tube 4–6 times. To avoid localized precipitation, mix the solution thoroughly, immediately after addition of Buffer N3. Large culture volumes (e.g. ≥5 ml) may require inverting up to 10 times. The solution should become cloudy.
-;Step 4
-:Centrifuge for 10 min at 13,000 rpm (~17,900 x g) in a table-top microcentrifuge. A compact white pellet will form.
-;Step 5
-:Apply the supernatants from step 4 to the QIAprep spin column by decanting or pipetting.
-;Step 6
-:Centrifuge for 30–60 s. Discard the flow-through.
-;Step 7
-:Recommended: Wash the QIAprep spin column by adding 0.5 ml Buffer PB and centrifuging for 30–60 s. Discard the flow-through.
-This step is necessary to remove trace nuclease activity when using endA+ strains such as the JM series, HB101 and its derivatives, or any wild-type strain, which have high levels of nuclease activity or high carbohydrate content. Host strains such as XL-1 Blue and DH5αTM do not require this additional wash step.
+#Resuspend pelleted bacterial cells in 250 μl Buffer P1 and transfer to a microcentrifuge tube. Ensure that RNase A has been added to Buffer P1. No cell clumps should be visible after resuspension of the pellet. If LyseBlue reagent has been added to Buffer P1, vigorously shake the buffer bottle to ensure LyseBlue particles are completely dissolved. The bacteria should be resuspended completely by vortexing or pipetting up and down until no cell clumps remain.
-;Step 8
+#Add 250 μl Buffer P2 and mix thoroughly by inverting the tube 4–6 times. Mix gently by inverting the tube. Do not vortex, as this will result in shearing of genomic DNA. If necessary, continue inverting the tube until the solution becomes viscous and slightly clear. Do not allow the lysis reaction to proceed for more than 5 min.
-:Wash QIAprep spin column by adding 0.75 ml Buffer PE and centrifuging for 30–60s.
+#Add 350 μl Buffer N3 and mix immediately and thoroughly by inverting the tube 4–6 times. To avoid localized precipitation, mix the solution thoroughly, immediately after addition of Buffer N3. Large culture volumes (e.g. ≥5 ml) may require inverting up to 10 times. The solution should become cloudy.
-;Step 9
+#Centrifuge for 10 min at 13,000 rpm (~17,900 x g) in a table-top microcentrifuge. A compact white pellet will form.
-:Discard the flow-through, and centrifuge for an additional 1 min to remove residual wash buffer. Important: Residual wash buffer will not be completely removed unless the flow-through is discarded before this additional centrifugation. Residual ethanol from Buffer PE may inhibit subsequent enzymatic reactions.
+#Apply the supernatants from step 4 to the QIAprep spin column by decanting or pipetting.
-;Step 10
+#Centrifuge for 30–60 s. Discard the flow-through.
-:Place the QIAprep column in a clean 1.5 ml microcentrifuge tube. To elute DNA, add 50 μl Buffer EB (10 mM Tris·Cl, pH 8.5) or water to the center of each QIAprep spin column, let stand for 1 min, and centrifuge for 1 min.
+#'''Recommended:''' Wash the QIAprep spin column by adding 0.5 ml Buffer PB and centrifuging for 30–60 s. Discard the flow-through.This step is necessary to remove trace nuclease activity when using endA+ strains such as the JM series, HB101 and its derivatives, or any wild-type strain, which have high levels of nuclease activity or high carbohydrate content. Host strains such as XL-1 Blue and DH5αTM do not require this additional wash step.
+#Wash QIAprep spin column by adding 0.75 ml Buffer PE and centrifuging for 30–60s.
+#Discard the flow-through, and centrifuge for an additional 1 min to remove residual wash buffer. '''Important:''' Residual wash buffer will not be completely removed unless the flow-through is discarded before this additional centrifugation. Residual ethanol from Buffer PE may inhibit subsequent enzymatic reactions.
+#Place the QIAprep column in a clean 1.5 ml microcentrifuge tube. To elute DNA, add 50 μl Buffer EB (10 mM Tris·Cl, pH 8.5) or water to the center of each QIAprep spin column, let stand for 1 min, and centrifuge for 1 min.
-===Safety===
-Some of the buffers used in this protocol contain potentially hazardous chemicals. Details can be found on the MSDS sheets [http://www.qiagen.com/support/msds.aspx?MSDSCountryID=UK&ddlKit=QIAprep+Spin+Miniprep+Kit&ddlKitText=QIAprep+Spin+Miniprep+Kit here].
+<center>'''[[Team:Cambridge/RiskAssessments/Miniprep|Risk Assessment]]'''</center>
+<center>'''[[Team:Cambridge/Protocols|Back to Protocols]]'''</center>
+<html>
-<center>'''[[Team:Cambridge/Protocols|Back to Protocols]]'''</center>
+</div>
+</html>
-{{Template:Team:Cambridge/CAM_2012_TEMPLATE_FOOT}}
+{{Template:Team:Cambridge/CAM_2012_TEMPLATE_FOOTNEW}}

Team:Cambridge/Protocols/MiniPrep

From 2012.igem.org

Latest revision as of 23:53, 26 October 2012

Contents

Judging Form

iGEM Medals for non-software teams

Requirements for a Bronze Medal

Additional Requirements for a Silver Medal

Additional Requirements for a Gold Medal: (one OR more)

iGEM Prizes

Please explain briefly why you should receive any of these special prizes:

Team_Parts

iGEM Safety

Attribution and Contributions

Comments

MiniPrep

Theory

Growing up cell cultures for miniprep

Preparation

Practice