Team:Kyoto/Project

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{{:Team:Kyoto/Header}}
{{:Team:Kyoto/Header}}
==Project==
==Project==
 +
[[Image:KyotoTop.png|600px|center]]
 +
===Abstract===
 +
<span class="title">'''The Fantastic Lysisbox:'''</span>
 +
Genetically engineered cell death is essential for the application of biotechnology, such as in bioremediation area. In order to control the cell-death, we designed “Lysisbox”, which consists of a pair of modules: “Killer gene” and “Anti-killer gene.” As the Killer gene for ''Escherichia coli'', we noted the lysis cassette [SRRz/Rz1 gene] of lambda phage coding for holin and endolysin. The holin form pores in the inner membrane and the endolysin access and degrade the peptidoglycan passing through the pores, leading the E.coli to death. As the Anti-killer gene, we chose S<sub>ΔTMD1</sub> coding for a dominant-negative holin that inhibits the formation of the fatal pores. The balance of these two genes' expression level has the key to the E.coli’s life or death. In addition, such controllable membrane pores should show critical functions for all living organisms with lipid membranes and a cell wall. “Lysisbox” will contribute a lot to all the future iGEM projects, thus you must say “FANTASTIC!!!"
===Introduction===
===Introduction===
====Background====
====Background====
-
The cell death devices are required in many areas. In bioremediation, for example, this device can help to prevent introduced bacteria from disrupting the native ecosystem. It can also be applied to other ideas like E.coli capsules which is scattering drug or aroma by lysing responding to a certain signal. Therefore, the cell death devices based on diverse approaches have been developed, including previous iGEM projects. However, using them is still not easy and convenient, for strict restriction on promoters’ activity narrows the possible application, the function of the device is not enough to reduce the population, and so on. Therefore, we attempt to register on biobrick more useful cell death device to contribute to every future team.
+
The cell-death device is required in many fields <sup>[[#RefH001|[1]]] [[#RefH002|[2]]]</sup>. In bioremediation, for example, this device can prevent ecosystem disruption by introduced bacteria <sup>[[#RefH003|[3]]] [[#RefH004|[4]]]</sup>. Also, it can be applied to other ideas such as E.coli capsules which scatter drug or aroma by cell-lysis responding to a certain signal. Therefore, the cell-death devices based on diverse approaches, including previous iGEM projects have been developed <sup>[[#RefH001|[1]]] [[#RefH003|[3]]] [[#RefH005|[5]]] [[#RefH006|[6]]]</sup>. However, present cell-death devices are not useful because they have two problems as follows:
-
====The problems of present Cell-death devices====
+
#'''They are not quantitatively characterized'''<sup>[[#RefH007|[7]]]</sup>
-
In order to design a universal and user-fridendly device, we need to tackle on mainly two issues: restriction on promoter-activity and the strength of the cell death function.  
+
#'''They are not applied to many promoters'''<sup>[[#RefH008|[8]]]</sup>.
-
The switch of cell-death function should be dependent only on a specific signal which activates the promoter but should not be affected largely by leaks. As an example, a simple circuit consists of inducible promoter and killer gene can cause this kind of problems. We try to widen the range of applicable promoters by combining the anti-killergene with the killergene.  
+
Therefore, we attempted to solve these problems and design new BioBricks that are better characterized and more applicable cell-death device to contribute to every future projects.
 +
[[Image:kyoto-intro.png|600px|center]]
-
As for the ability of killing cell itself, we consider the lysis cassette of lambda phage is the most appropriate genes for this project among other candidates for killer gene we searched. It is because we found the data showing the lytic system is able to lead annihilation though some can only regulate cell proliferation at a certain population of the bacteria, and also the lysis cassette consists of anti-killergene and killer gene.
+
====Problems of Present Cell-Death Devices====
 +
=====1.Need for Quantitative Characterization=====
 +
In previous iGEM, many teams focused on &lambda; lysis cassette, which is a killer-gene derived from &lambda; phage and causes cell lysis. However, they have only characterized its lytic activity qualititatively. Quantitative characterization of its lytic activity is necessary in order to design a universal and applicable cell-death device. For example, we wish to analyze when cell lysis occurs after induction of λ lysis cassette, how many cells lyse, whether all of cells lyse or not, and so on.
-
====Lytic system derived from lambda phage====
+
=====2. Solution to the Restriction on Application of Promoters=====
-
We take advantage of the lambda phage’s lysis cassette as killer gene, which consists of four genes: S, R, coding for holin, endolysin, respectively, and Rz/Rz1 gene. In this lytic system, endolysin accesses through the pores on cell membrane formed by holin, and degrade peptidoglycan, leading to E.coli to die. As anti-killer gene, we use SΔTMD1 cording for dominant-negative holin, which is deleted the first trans-membrane domein-TMD1 of wild type holin. This variant holin prevents holin from forming pores, and endolysin cannot access peptidoglycan.
+
In constructing a simple circuit consisting of an inducible promoter and &lambda; lysis cassette, the combination are limited by the promoter's basal expression, strength of killer-function and many other factors.  
 +
We looked for the solution to this problem and came up with an idea; using both the lysis cassette and its antikiller-gene, S<sub>&Delta;TMD1</sub>, which lacks the code for trans membrane domain 1 of killer-gene. We can use two promoters (a constitutive one and an inducible one) for regulating cell-death balance. Into this circuit, we can apply more promoters to this device by using an appropriate constitutive promoter.
 +
We considered that lysis cassette and S<sub>&Delta;TMD1</sub> are the most appropriate to killer-gene and anti-killer gene <sup>[[#RefH005|[5]]]</sup>. This was because we found some articles which show the effect of S<sub>&Delta;TMD1</sub> in the yeast <sup>[[#RefH009|[9]]]</sup> and also because previous iGEM teams already dealt with lysis cassette.
 +
For further description about lysis cassette and S<sub>&Delta;TMD1</sub>, go [[Team:Kyoto/LearnMore#Lysis Cassette|[learn more]]]
-
[[#Top|^Top]]
+
===Our Goals===
 +
====[[Team:Kyoto/Project/Goal A|Goal A: Characterization of R0011, a strong lactose promoter]]====
 +
[[Image:KyotoGoalA.png|450px|left]]
 +
We used R0011, which is one of the most commonly used parts in iGEM, to characterize our genes because the strength of promoter activity is very high. However, in previous iGEM, no teams characterized R0011 with RPU. We tried to determine how the activity of R0011<sup>[[#RefH010|[10]]]</sup> changes.
 +
[[Image:KyotoGrpA003.png|450px|left]]
-
===Overview===
+
<div style="float:right;">[[Team:Kyoto/Project/Goal A|<html><img src="http://2010.igem.org/wiki/images/thumb/1/12/KyotoArrowA.png/200px-KyotoArrowA.png"/></html>]]</div>
-
====Goal A Characterization of R0011, a strong lactose promoter====
+
{{clear}}
-
We used R0011, which is one of the most commonly used parts in iGEM, to characterize our genes
+
-
because the strength of promoter activity is very high.However, in previous iGEM, no teams didn't characterize R0011 with RPU.  
+
-
We tried to determine what is the ratio of activity of R0011,a lactose promoter when cell lysis occurs. Therefore, in oreder to characterize 'lysis box', we have to characterize R0011.  
+
====[[Team:Kyoto/Project/Goal B|Goal B: Quantitative characterization of &lambda; lysis cassette]]====
 +
[[Image:KyotoGoalB.png|450px|left]]
 +
[[Image:KyotoFigC004.png|450px]]<br/>
 +
We found a new fact that cell lysis caused by λ lysis cassette become an apparent equilibrium state, and the value of OD550 depends on the strength of induction of IPTG. We defiend it as LAV (Lytic Activity Value) as a quantitative parameter of lytic activity, and we established a standard method for lytic activity of  &lambda; lysis cassette. We characterized the lytic activity of &lambda; lysis cassette quantitatively as our established method, and linked the result to the strength of induction(RPU).
-
For the characterization of R0011, we moved R0011 onto pSB4K5, a low copy vector, and transformed it into E.coli KRX, the strain overexpressing lacI, so that R0011 is repressed fully at low IPTG concentraion. RPU (Relative Promoter Unit) is used to describe the activity of RPU, and GFP is used as a reporter. KRX transformed with BBa_I20260 is also used.
+
We characterized the lytic ativity of λ lysis cassette with time.  
 +
{{clear}}
 +
[[Image:KyotofigD002.png|450px|left|]]
 +
[[Image:KyotoGrp101028-1.png|450px]]
 +
<div style="float:right;">[[Team:Kyoto/Project/Goal B|<html><img src="http://2010.igem.org/wiki/images/thumb/a/ac/KyotoArrowB.png/200px-KyotoArrowB.png"/></html>]]</div>
 +
{{clear}}
-
====Goal B Characterization of λLysis cassette====
+
====[[Team:Kyoto/Project/Goal C|Goal C: Characterization of the anti-killer gene, S&Delta;TMD1]]====
-
To characterize λlysiscassette, we made below construct and observed E.coli transformed  
+
[[Image:KyotoGoalC.png|460px|left]]
-
with the constructs in various concentration of IPTG.
+
[[Image:KyotoFigC003.png|460px]]<br/>
 +
To check function of the anti-killer gene, first, we made construct and measured A550 of E.coli transformed with the device in medium with IPTG and without IPTG, and we compared this result with that of E.coli transformed with killer gene, lysis cassette. Then, we were able to make sure that Transmembrane domein1 (TMD1) is essential for , lysis cassette.
 +
{{clear}}
 +
[[Image:GoalC fig3-2-2.png|450px]]
 +
<div style="float:right;">[[Team:Kyoto/Project/Goal C|<html><img src="http://2010.igem.org/wiki/images/thumb/e/ea/KyotoArrowC.png/200px-KyotoArrowC.png"/></html>]]</div>
 +
{{clear}}
-
====Goal C Characterization of the anti-killer gene====
+
[[#top-section|^Top]]
-
E.coli transformed with the constructs below was grown in medium without IPTG and IPTG was added to the culture at proper time. The A550 of the culture was measured  and the result was compared with that of the experiment of the killer gene in order to find whether the killer gene works correctly.
+
-
===Protocols===
+
===Achievement===
-
See below pages for details.
+
# We measured RPU of R0011 in eight kinds of concentration of IPTG, and made continuous curve '''representing the relation between concentration of IPTG and RPU of R0011''' by simulation fitting.
-
* [[Team:Kyoto/Protocols|Protocols]]
+
# We '''characterized the lytic activity''' of λ lysis cassette quantitatively as our established method,and linked the result to the strength of induction (RPU).
-
* [[Team:Kyoto/Materials|Materials]]
+
# We '''found that a new fact''' that cell lysis caused by λ lysis cassette become an apparent equilibrium state, and the value of OD550 depends on the strength of induction of IPTG. We defined it as LAV(Lytic Activity Value)as a quantitative parameter of lytic activity, and '''we established a standard''' method for lytic activity of λ lysis cassette.
 +
# We '''checked the activity of S<sub>ΔTMD1</sub>''', which can't form pore of holin and cells don't die although endolysin expresses.
-
===Notebook===
+
[[#top-section|^Top]]
-
* [[Team:Kyoto/Notebook/Construction|Construction for Lysisbox]]
+
-
* [[Team:Kyoto/Notebook/Measurement|Measurement of Lysisbox]]
+
-
* [[Team:Kyoto/Notebook/LacPromoter|Characterization of R0011 (Lactose Promoter)]]
+
-
[[#Top|^Top]]
 
-
===References===
 
-
# [http://www.ncbi.nlm.nih.gov/pubmed/20395970 PMID: 20395970] Khalil AS, Collins JJ., Synthetic biology: applications come of age., Nat Rev Genet. 2010 May;11(5):367-79.
 
-
# [http://www.ncbi.nlm.nih.gov/pubmed/15832375 PMID: 15832375] Paul D, Pandey G, Jain RK., Suicidal genetically engineered microorganisms for bioremediation: need and perspectives., Bioessays. 2005 May;27(5):563-73.
 
-
# [http://www.ncbi.nlm.nih.gov/pubmed/15973534 PMID: 15973534] Davison J., Risk mitigation of genetically modified bacteria and plants designed for bioremediation., J Ind Microbiol Biotechnol. 2005 Dec;32(11-12):639-50. Epub 2005 Jun 23.
 
-
# [http://www.ncbi.nlm.nih.gov/pubmed/19897658 PMID: 19897658] White R, Tran TA, Dankenbring CA, Deaton J, Young R., The N-terminal transmembrane domain of lambda S is required for holin but not antiholin function., J Bacteriol. 2010 Feb;192(3):725-33. Epub 2009 Nov 6.
 
-
# [http://www.ncbi.nlm.nih.gov/pubmed/7768829 PMID: 7768829] Chang CY, Nam K, Young R., S gene expression and the timing of lysis by bacteriophage lambda., J Bacteriol. 1995 Jun;177(11):3283-94.
 
-
# [http://www.ncbi.nlm.nih.gov/pubmed/18713319 PMID: 18713319] Berry J, Summer EJ, Struck DK, Young R., The final step in the phage infection cycle: the Rz and Rz1 lysis proteins link the inner and outer membranes., Mol Microbiol. 2008 Oct;70(2):341-51. Epub 2008 Aug 18.
 
-
# [http://www.ncbi.nlm.nih.gov/pubmed/11459934 PMID: 11459934] Gründling A, Manson MD, Young R., Holins kill without warning., Proc Natl Acad Sci U S A. 2001 Jul 31;98(16):9348-52. Epub 2001 Jul 17.
 
-
# [http://www.ncbi.nlm.nih.gov/pubmed/9573208 PMID: 9573208] Smith DL, Struck DK, Scholtz JM, Young R., Purification and biochemical characterization of the lambda holin., J Bacteriol. 1998 May;180(9):2531-40.
 
-
# [http://www.ncbi.nlm.nih.gov/pubmed/19298678 PMID: 19298678] Kelly JR, Rubin AJ, Davis JH, Ajo-Franklin CM, Cumbers J, Czar MJ, de Mora K, Glieberman AL, Monie DD, Endy D., Measuring the activity of BioBrick promoters using an in vivo reference standard., J Biol Eng. 2009 Mar 20;3:4.
 
-
# [http://www.ncbi.nlm.nih.gov/pubmed/2147680 PMID: 2147680] Garrett J, Bruno C, Young R., Lysis protein S of phage lambda functions in Saccharomyces cerevisiae., J Bacteriol. 1990 Dec;172(12):7275-7.
 
-
[[#Top|^Top]]
+
===Future work===
 +
1. Characterization of S<sub>&Delta;TMD1</sub> quantitatively
 +
 
 +
We checked the function of S<sub>&Delta;TMD1</sub>, however, we couldn’t confirm that S<sub>&Delta;TMD1</sub>can inhibit S gene when S<sub>&Delta;TMD1</sub> expresses simultaneously.
 +
We think this is because the expression level of S<sub>&Delta;TMD1</sub> is too low to inhibit the  activity of S gene in the experiment. By Jamboree, using more strong promoter to express S<sub>&Delta;TMD1</sub>, we check the function of S<sub>&Delta;TMD1</sub>, which prevents cell-lysis.
 +
 
 +
2. Change the point of cell lysis and make lysis cassette more useful device.
 +
 
 +
We used the inducible promoter to express S gene and measured what the promoter activity leads cell to lyse. Such experiment suggests that there is the threshold for cell lysis caused by lysis cassette. By expressing S<sub>&Delta;TMD1</sub>, we can make cell lysis at higher expression level, and change the threshold of the cell lysis.
 +
 
 +
If lysis cassette expressed by promoters which cannot exceed this threshold, cell lysis does not occur.
 +
Expression of S<sub>&Delta;TMD1</sub> by constitutive promoter may inhibit the activity of lysis cassette and increase the threshold.
 +
Therefore, we can regulate cell lysis by controlling expression level of S<sub>&Delta;TMD1</sub>.
 +
Besides, by characterizing of the relationship between cell lysis and the balance between S gene and S<sub>&Delta;TMD1</sub> with RPU, we can control cell lysis easily with promoters characterized by RPU in the partsregistry….
 +
There are many kinds of well- characterized constitutive promoter in the partsregistry.
 +
 
 +
[[#top-section|^Top]]
 +
 
 +
===References===
 +
# <html><a name="RefH001"></a></html> [http://www.ncbi.nlm.nih.gov/pubmed/20395970 PMID: 20395970] Khalil AS, Collins JJ., Synthetic biology: applications come of age., Nat Rev Genet. 2010 May;11(5):367-79.
 +
# <html><a name="RefH002"></a></html> [http://www.ncbi.nlm.nih.gov/pubmed/15832375 PMID: 15832375] Paul D, Pandey G, Jain RK., Suicidal genetically engineered microorganisms for bioremediation: need and perspectives., Bioessays. 2005 May;27(5):563-73.
 +
# <html><a name="RefH003"></a></html> [http://www.ncbi.nlm.nih.gov/pubmed/15973534 PMID: 15973534] Davison J., Risk mitigation of genetically modified bacteria and plants designed for bioremediation., J Ind Microbiol Biotechnol. 2005 Dec;32(11-12):639-50. Epub 2005 Jun 23.
 +
# <html><a name="RefH004"></a></html>http://2009.igem.org/Team:Michigan
 +
# <html><a name="RefH005"></a></html> [http://www.ncbi.nlm.nih.gov/pubmed/19897658 PMID: 19897658] White R, Tran TA, Dankenbring CA, Deaton J, Young R., The N-terminal transmembrane domain of lambda S is required for holin but not antiholin function., J Bacteriol. 2010 Feb;192(3):725-33. Epub 2009 Nov 6.
 +
# <html><a name="RefH006"></a></html>http://2009.igem.org/Team:UNICAMP-Brazil
 +
# <html><a name="RefH007"></a></html>http://2008.igem.org/Team:UC_Berkeley
 +
# <html><a name="RefH008"></a></html> [http://www.ncbi.nlm.nih.gov/pubmed/18713319 PMID: 18713319] Berry J, Summer EJ, Struck DK, Young R., The final step in the phage infection cycle: the Rz and Rz1 lysis proteins link the inner and outer membranes., Mol Microbiol. 2008 Oct;70(2):341-51. Epub 2008 Aug 18.
 +
# <html><a name="RefH009"></a></html> [http://www.ncbi.nlm.nih.gov/pubmed/2147680 PMID: 2147680] Garrett J, Bruno C, Young R., Lysis protein S of phage lambda functions in Saccharomyces cerevisiae., J Bacteriol. 1990 Dec;172(12):7275-7.
 +
# <html><a name="RefH010"></a></html> [http://www.ncbi.nlm.nih.gov/pubmed/19298678 PMID: 19298678] Kelly JR, Rubin AJ, Davis JH, Ajo-Franklin CM, Cumbers J, Czar MJ, de Mora K, Glieberman AL, Monie DD, Endy D., Measuring the activity of BioBrick promoters using an in vivo reference standard., J Biol Eng. 2009 Mar 20;3:4.
 +
# <html><a name="RefH011"></a></html> [http://www.ncbi.nlm.nih.gov/pubmed/7768829 PMID: 7768829] Chang CY, Nam K, Young R., S gene expression and the timing of lysis by bacteriophage lambda., J Bacteriol. 1995 Jun;177(11):3283-94.
 +
# <html><a name="RefH012"></a></html> [http://www.ncbi.nlm.nih.gov/pubmed/11459934 PMID: 11459934] Gründling A, Manson MD, Young R., Holins kill without warning., Proc Natl Acad Sci U S A. 2001 Jul 31;98(16):9348-52. Epub 2001 Jul 17.
 +
# <html><a name="RefH013"></a></html> [http://www.ncbi.nlm.nih.gov/pubmed/9573208 PMID: 9573208] Smith DL, Struck DK, Scholtz JM, Young R., Purification and biochemical characterization of the lambda holin., J Bacteriol. 1998 May;180(9):2531-40.
 +
[[#top-section|^Top]]
----
----

Latest revision as of 10:52, 18 November 2010

Contents

Project

KyotoTop.png

Abstract

The Fantastic Lysisbox: Genetically engineered cell death is essential for the application of biotechnology, such as in bioremediation area. In order to control the cell-death, we designed “Lysisbox”, which consists of a pair of modules: “Killer gene” and “Anti-killer gene.” As the Killer gene for Escherichia coli, we noted the lysis cassette [SRRz/Rz1 gene] of lambda phage coding for holin and endolysin. The holin form pores in the inner membrane and the endolysin access and degrade the peptidoglycan passing through the pores, leading the E.coli to death. As the Anti-killer gene, we chose SΔTMD1 coding for a dominant-negative holin that inhibits the formation of the fatal pores. The balance of these two genes' expression level has the key to the E.coli’s life or death. In addition, such controllable membrane pores should show critical functions for all living organisms with lipid membranes and a cell wall. “Lysisbox” will contribute a lot to all the future iGEM projects, thus you must say “FANTASTIC!!!"

Introduction

Background

The cell-death device is required in many fields [1] [2]. In bioremediation, for example, this device can prevent ecosystem disruption by introduced bacteria [3] [4]. Also, it can be applied to other ideas such as E.coli capsules which scatter drug or aroma by cell-lysis responding to a certain signal. Therefore, the cell-death devices based on diverse approaches, including previous iGEM projects have been developed [1] [3] [5] [6]. However, present cell-death devices are not useful because they have two problems as follows:

  1. They are not quantitatively characterized[7]
  2. They are not applied to many promoters[8].

Therefore, we attempted to solve these problems and design new BioBricks that are better characterized and more applicable cell-death device to contribute to every future projects.

Kyoto-intro.png

Problems of Present Cell-Death Devices

1.Need for Quantitative Characterization

In previous iGEM, many teams focused on λ lysis cassette, which is a killer-gene derived from λ phage and causes cell lysis. However, they have only characterized its lytic activity qualititatively. Quantitative characterization of its lytic activity is necessary in order to design a universal and applicable cell-death device. For example, we wish to analyze when cell lysis occurs after induction of λ lysis cassette, how many cells lyse, whether all of cells lyse or not, and so on.


2. Solution to the Restriction on Application of Promoters

In constructing a simple circuit consisting of an inducible promoter and λ lysis cassette, the combination are limited by the promoter's basal expression, strength of killer-function and many other factors. We looked for the solution to this problem and came up with an idea; using both the lysis cassette and its antikiller-gene, SΔTMD1, which lacks the code for trans membrane domain 1 of killer-gene. We can use two promoters (a constitutive one and an inducible one) for regulating cell-death balance. Into this circuit, we can apply more promoters to this device by using an appropriate constitutive promoter.

We considered that lysis cassette and SΔTMD1 are the most appropriate to killer-gene and anti-killer gene [5]. This was because we found some articles which show the effect of SΔTMD1 in the yeast [9] and also because previous iGEM teams already dealt with lysis cassette.

For further description about lysis cassette and SΔTMD1, go [learn more]

Our Goals

Goal A: Characterization of R0011, a strong lactose promoter

KyotoGoalA.png

We used R0011, which is one of the most commonly used parts in iGEM, to characterize our genes because the strength of promoter activity is very high. However, in previous iGEM, no teams characterized R0011 with RPU. We tried to determine how the activity of R0011[10] changes.

KyotoGrpA003.png

Goal B: Quantitative characterization of λ lysis cassette

KyotoGoalB.png

KyotoFigC004.png
We found a new fact that cell lysis caused by λ lysis cassette become an apparent equilibrium state, and the value of OD550 depends on the strength of induction of IPTG. We defiend it as LAV (Lytic Activity Value) as a quantitative parameter of lytic activity, and we established a standard method for lytic activity of λ lysis cassette. We characterized the lytic activity of λ lysis cassette quantitatively as our established method, and linked the result to the strength of induction(RPU).

We characterized the lytic ativity of λ lysis cassette with time.

KyotofigD002.png

KyotoGrp101028-1.png

Goal C: Characterization of the anti-killer gene, SΔTMD1

KyotoGoalC.png

KyotoFigC003.png
To check function of the anti-killer gene, first, we made construct and measured A550 of E.coli transformed with the device in medium with IPTG and without IPTG, and we compared this result with that of E.coli transformed with killer gene, lysis cassette. Then, we were able to make sure that Transmembrane domein1 (TMD1) is essential for , lysis cassette.

GoalC fig3-2-2.png

^Top

Achievement

  1. We measured RPU of R0011 in eight kinds of concentration of IPTG, and made continuous curve representing the relation between concentration of IPTG and RPU of R0011 by simulation fitting.
  2. We characterized the lytic activity of λ lysis cassette quantitatively as our established method,and linked the result to the strength of induction (RPU).
  3. We found that a new fact that cell lysis caused by λ lysis cassette become an apparent equilibrium state, and the value of OD550 depends on the strength of induction of IPTG. We defined it as LAV(Lytic Activity Value)as a quantitative parameter of lytic activity, and we established a standard method for lytic activity of λ lysis cassette.
  4. We checked the activity of SΔTMD1, which can't form pore of holin and cells don't die although endolysin expresses.

^Top


Future work

1. Characterization of SΔTMD1 quantitatively

We checked the function of SΔTMD1, however, we couldn’t confirm that SΔTMD1can inhibit S gene when SΔTMD1 expresses simultaneously. We think this is because the expression level of SΔTMD1 is too low to inhibit the activity of S gene in the experiment. By Jamboree, using more strong promoter to express SΔTMD1, we check the function of SΔTMD1, which prevents cell-lysis.

2. Change the point of cell lysis and make lysis cassette more useful device.

We used the inducible promoter to express S gene and measured what the promoter activity leads cell to lyse. Such experiment suggests that there is the threshold for cell lysis caused by lysis cassette. By expressing SΔTMD1, we can make cell lysis at higher expression level, and change the threshold of the cell lysis.

If lysis cassette expressed by promoters which cannot exceed this threshold, cell lysis does not occur. Expression of SΔTMD1 by constitutive promoter may inhibit the activity of lysis cassette and increase the threshold. Therefore, we can regulate cell lysis by controlling expression level of SΔTMD1. Besides, by characterizing of the relationship between cell lysis and the balance between S gene and SΔTMD1 with RPU, we can control cell lysis easily with promoters characterized by RPU in the partsregistry…. There are many kinds of well- characterized constitutive promoter in the partsregistry.

^Top

References

  1. PMID: 20395970 Khalil AS, Collins JJ., Synthetic biology: applications come of age., Nat Rev Genet. 2010 May;11(5):367-79.
  2. PMID: 15832375 Paul D, Pandey G, Jain RK., Suicidal genetically engineered microorganisms for bioremediation: need and perspectives., Bioessays. 2005 May;27(5):563-73.
  3. PMID: 15973534 Davison J., Risk mitigation of genetically modified bacteria and plants designed for bioremediation., J Ind Microbiol Biotechnol. 2005 Dec;32(11-12):639-50. Epub 2005 Jun 23.
  4. http://2009.igem.org/Team:Michigan
  5. PMID: 19897658 White R, Tran TA, Dankenbring CA, Deaton J, Young R., The N-terminal transmembrane domain of lambda S is required for holin but not antiholin function., J Bacteriol. 2010 Feb;192(3):725-33. Epub 2009 Nov 6.
  6. http://2009.igem.org/Team:UNICAMP-Brazil
  7. http://2008.igem.org/Team:UC_Berkeley
  8. PMID: 18713319 Berry J, Summer EJ, Struck DK, Young R., The final step in the phage infection cycle: the Rz and Rz1 lysis proteins link the inner and outer membranes., Mol Microbiol. 2008 Oct;70(2):341-51. Epub 2008 Aug 18.
  9. PMID: 2147680 Garrett J, Bruno C, Young R., Lysis protein S of phage lambda functions in Saccharomyces cerevisiae., J Bacteriol. 1990 Dec;172(12):7275-7.
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