Team:Newcastle/9 August 2010

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{{Team:Newcastle/mainbanner}}
{{Team:Newcastle/mainbanner}}
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=Transformation of pVeg and lacI=
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=Subtilin immunity part=
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==Results/Aims==
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* There are colonies on all 3 plates for pVeg.
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* For ''lacI'', there is only one colony on one of the normal plates and more on the concentrated one.
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==Discussion==
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* For pVeg, we will set up an [[Team:Newcastle/Growing_an_overnight_cultures|overnight broth culture]] from the colonies for [[Team:Newcastle/Qiagen_Minipreps|plasmid extraction]]
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* To show that we have sucessfully transformed from ''lacI'', we will select 4 colonies and plate them on a section of an agar plate as well as setting up overnight broth cultures.
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==Conclusion==
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Please refer to [[Team:Newcastle/10_August_2010|10.08.10]].
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=Transformation of lacI=
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==Aims==
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To transform some competent ''E.coli'' DH5α with the ligation products: 1:3, 1:5 and the vector from the ligation on [[Team:Newcastle/6_August_2010|06.08.10]].
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==Materials and Protocol==
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Please refer to [[TeamNewcastleTransformation_of_E._coli|Transformation of E.coli]].
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==Result==
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Please refer to [[Team:Newcastle/10_August_2010|10.08.10]] for result.
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=Amplification of Pspac_oid promoter by PCR=
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==Aim==
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The aim of this experiment is to amplify Pspac_oid promoter fragment from plasmid pMutin4 for the construction of [[Team:Newcastle/Urease|''rocF'' BioBrick]] with the help of 2 different Phusion PCR.
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==Materials and Protocol==
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Please refer to  [[Team:Newcastle/PCR| PCR]] for Phusion PCR protocol. The details for the 4 PCR reactions are mentioned below:
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===PCR===
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{|border=1
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|-
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!'''Tube'''
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!'''Part to be amplified'''
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!'''DNA fragment consisting the part'''
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!'''Forward primer'''
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!'''Reverse Primer'''
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!'''Melting Temperature (Tm in °C) '''
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!'''Size of the fragment (in bp)'''
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!'''Extension time* (in seconds)'''
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|-
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|1
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|Pspacoid Promoter
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|pMutin4
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|P1P1 forward
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|P2P1 reverse
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|58
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|106 approx.
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|15
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|-
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|2
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|Pspacoid Promoter
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|pMutin4
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|P1P1 forward
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|P2P1 reverse
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|59
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|106 approx.
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|15
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|}
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'''Table 1''': Table represents 4 different Phusion PCR reactions for the amplification of Pspac_oid promoter, so that it can be ligated together with other fragments for the construction of ''rocF'' with the help of Gibson Cloning method.
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* The extension rate of the Phusion polymerase is 1Kb/ 30 seconds. Thus the extension time of each and every PCR reaction is slightly different.
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* For learning about the ''rocF'' fragments, please refer to the [[Media:Cloning_strategy_for_rocF.pdf|Cloning strategy for ''rocF'']].
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==Discussion==
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All the 2 Phusion PCR reactions were done however, gel electrophoresis will be done later today, to check whether the fragments have actually amplified or not.
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==Conclusion==
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Today afternoon, we would be running gel electrophoresis to check the outcome of the 2 PCR reactions and later all the fragments will be ligated with help of Gibson protocol if the fragments have amplified.
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=Amplification of Pspac_oid promoter by PCR=
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==Aim==
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The aim of this experiment is to amplify Pspac_oid promoter fragment from plasmid pMK-RQ containing Biobrick ''kinA'' and plasmid pMK-RQ containing stochastic switch developed by Team Newcastle 2009 for the construction of [[Team:Newcastle/Urease|''rocF'' BioBrick]] with the help of 4 different Phusion PCR.
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==Materials and Protocol==
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Please refer to  [[Team:Newcastle/PCR| PCR]] for Phusion PCR protocol. The details for the 2 PCR reactions are mentioned below:
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===PCR===
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{|border=1
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|-
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!'''Tube'''
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!'''Part to be amplified'''
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!'''DNA fragment consisting the part'''
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!'''Forward primer'''
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!'''Reverse Primer'''
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!'''Melting Temperature (Tm in °C) '''
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!'''Size of the fragment (in bp)'''
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!'''Extension time* (in seconds)'''
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|-
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|1
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|Pspacoid Promoter
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|Plasmid containing ''kinA''
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|P1P1 forward
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|P2P1 reverse
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|58
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|106 approx.
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|15
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|-
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|2
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|Pspacoid Promoter
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|Plasmid containing ''kinA''
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|P1P1 forward
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|P2P1 reverse
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|59
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|106 approx.
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|15
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|-
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|3
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|Pspacoid Promoter
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|Plasmid containing stochastic switch
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|P1P1 forward
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|P2P1 reverse
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|58
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|106 approx.
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|15
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|-
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|1
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|Pspacoid Promoter
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|Plasmid containing stochastic switch
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|P1P1 forward
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|P2P1 reverse
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|59
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|106 approx.
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|15
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|}
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'''Table 2''': Table represents 2 different Phusion PCR reactions for the amplification of Pspac_oid promoter, so that it can be ligated together with other fragments for the construction of ''rocF'' with the help of Gibson Cloning method.
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* The extension rate of the Phusion polymerase is 1Kb/ 30 seconds. Thus the extension time of each and every PCR reaction is slightly different.
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* For learning about the ''rocF'' fragments, please refer to the [[Media:Cloning_strategy_for_rocF.pdf|Cloning strategy for ''rocF'']].
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==Discussion==
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All the 4 Phusion PCR reactions were done however, gel electrophoresis will be done later today, to check whether the fragments have actually amplified or not.
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==Conclusion==
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Today afternoon, we would be running gel electrophoresis to check the outcome of the 4 PCR reactions and later all the fragments will be ligated with help of Gibson protocol if the fragments have amplified.
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=Gel Electrophoresis for Amplified Pspac_oid promoter and ''lacI''=
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==Aim==
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The aim of the experiment is to perform gel electrophoresis for the two PCR reactions viz. ''lacI'' and Pspac_oid promoter which took place yesterday 5th August, 2010 and thus confirm that they were successful.
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==Materials and Protocol==
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Please refer to: [[Team:Newcastle/Gel electrophoresis| Gel electrophoresis]].
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==Result==
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[[Image:Newcastle_060810_gel_1.png|400px]]
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'''Figure 1''': Gel electrophoresis of the ''lacI'' and  Pspac_oid promoter.
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* '''Lane 1''': 1kb DNA ladder
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* '''Lane 2''': Plamid pMutin4 containing ''lacI''
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* '''Lane 3''': Plamid pMutin4 containing Pspac_oid promoter
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* '''Lane 4''': 100bp DNA ladder
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{|border=1
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|-
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!
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!'''Pspac_oid pormoter'''
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!'''''lacI'''''
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|'''Size of the Fragment (in bp)'''
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|106 approx.
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|1400 approx.
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'''Table 1''': Table represents the size of the fragments represented as bands on the gel in their corresponding lanes.
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==Discussion==
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We found a band in the lanes 2 of the correct size but lane 3 did not contain any band.
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==Conclusion==
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This experiment shows that the PCR reaction was successful for the ''lacI'' fragment apart from Pspac_oid promoter which was present in the lane 3 and did not show any band. As we got a band for ''lacI'', we can conclude that the plasmid pMutin4 is intact. But we still are not getting a band for Pspac_oid pomoter. This could be because of the following problem:
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# Melting temperature could be incorrect.
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=Transformation of hyperspank and spoVG=
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==Aim==
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To transform competent E.coli DH5α with hyperspank and spoVG.
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==Materials and Protocol==
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Please refer to [[TeamNewcastleTransformation_of_E._coli|transformation of E.coli]].
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Today we were working on our subtilin immunity part cloning strategy.
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{{Team:Newcastle/footer}}

Latest revision as of 23:03, 27 October 2010

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Subtilin immunity part

Today we were working on our subtilin immunity part cloning strategy.

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