Edinburgh/Notebook/PCR products

From 2008.igem.org

(Difference between revisions)
(New page: <html> <head> <title>Edinburgh iGem 2008</title> <script type="text/javascript"> //Drop Down Tabs Menu- Author: Dynamic Drive (http://www.dynamicdrive.com) //Created: May 16th, 07' var ta...)
 
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<html>
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<div id="header">{{Template:Team:Edinburgh/Templates/Header}}</div>
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<head>
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<title>Edinburgh iGem 2008</title>
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<script type="text/javascript">
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//Drop Down Tabs Menu- Author: Dynamic Drive (http://www.dynamicdrive.com)
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//Created: May 16th, 07'
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var tabdropdown={
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'''[[Team:Edinburgh/Notebook|< Back to Notebook]]'''
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disablemenuclick: false, //when user clicks on a menu item with a drop down menu, disable menu item's link?
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enableiframeshim: 1, //1 or 0, for true or false
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//No need to edit beyond here////////////////////////
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== PCR Products ==
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dropmenuobj: null, ie: document.all, firefox: document.getElementById&&!document.all, previousmenuitem:null,
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'''P1:''' ''dxs'' from ''Escherichia coli'' JM109. (25.06.08)<br />
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currentpageurl: window.location.href.replace("http://"+window.location.hostname, "").replace(/^\//, ""), //get current page url (minus hostname, ie: http://www.dynamicdrive.com/)
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'''P2:''' ''appY'' from ''E. coli'' JM109. (25.06.08)<br />
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'''P3:''' ''glgC'' from ''E. coli'' JM109. (25.06.08)<br />
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getposOffset:function(what, offsettype){
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'''P4:''' Fusion PCR for BABEL1+''glgC''. (01.07.08)<br />
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var totaloffset=(offsettype=="left")? what.offsetLeft : what.offsetTop;
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'''P5:''' Fusion PCR for BABEL2+''glgC''. (01.07.08)<br />
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var parentEl=what.offsetParent;
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'''P6:''' Mutagenic PCR to remove EcoRI site 1 from ''glgC'' (M11). (04.07.08)<br />
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while (parentEl!=null){
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'''P7:''' Mutagenic PCR to remove EcoRI site 2 from ''glgC'' (M11). (04.07.08)<br />
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totaloffset=(offsettype=="left")? totaloffset+parentEl.offsetLeft : totaloffset+parentEl.offsetTop;
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'''P8:''' ''crtB'' (from ''Pantoea ananatis'' cells). (08.07.08)<br />
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parentEl=parentEl.offsetParent;
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'''P9:''' ''crtI'' (from Douglas's maxiprep of the mutated ''crtIB'' plasmid). (08.07.08)<br />
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}
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'''P10:''' ''crtY'' (from ''P. ananatis'' cells). Failed. (08.07.08)<br />
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return totaloffset;
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'''P11:''' Fusion PCR of rbs+''dxs''. Failed. (10.07.08)<br />
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},
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'''P12:''' Repeat fusion PCR of rbs+''dxs'', using L11 and primers rbs2fclon1+pSB1A2insr1. (13.07.08)<br />
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'''P13-P14:''' MABEL mutation of site 1 on ''glgC''-mut2 clones M19 and M22. (14.07.08)<br />
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showhide:function(obj, e, obj2){ //obj refers to drop down menu, obj2 refers to tab menu item mouse is currently over
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'''P15:''' Rusion PCR for rbs+''appY'' using L15 as a template. (15.07.08)<br />
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if (this.ie || this.firefox)
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'''P16-P19:''' First attempts at ''cenA'', ''cenB'', ''cenC'' and ''cex''. (17.07.08) - Failed<br />
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this.dropmenuobj.style.left=this.dropmenuobj.style.top="-500px"
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'''P20-P23:''' Second attempts at ''cenA'', ''cenB'', ''cenC'' and ''cex''. (18.07.08) - Failed<br />
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if (e.type=="click" && obj.visibility==hidden || e.type=="mouseover"){
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'''P24-P25:''' Repeat PCR for ''cenA'' and ''cex'' using Pfu. (19.07.08) - Failed<br />
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if (obj2.parentNode.className.indexOf("default")==-1) //if tab isn't a default selected one
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'''P26:''' Positive control PCR with primers fd1 and rd1 to amplify 16S rRNA gene ''rrnB'' from ''C. fimi''. (22.07.08: AM) - Failed<br />
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obj2.parentNode.className="selected"
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'''P27:''' ''crtY'' from ''P. ananatis'' cells. (23.07.08: AM, Yan, OG) - Failed<br />
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obj.visibility="visible"
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'''P28:''' Fusion PCR of rbs+''crtB'' from L18. (23.07.08: AM, Yan, OG)<br />
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}
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'''P29:''' Fusion PCR of rbs+''crtI'' from L19. (23.07.08: AM, Yan, OG)<br />
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else if (e.type=="click")
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'''P30:''' Repeat positive control of ''rrnB'' from ''C. fimi'', annealing 1 minute. (23.07.08: AM)<br />
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/* ######### Style for Drop Down Menu ######### */
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.dropmenudiv_a{
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.dropmenudiv_a a:hover{ /*THEME CHANGE HERE*/
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</head>
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<!-- CSS for Drop Down Tabs Menu #1 -->
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<link rel="stylesheet" type="text/css" href="ddcolortabs.css" />
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<div id="colortab" class="ddcolortabs">
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<ul>
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<li><a href="https://2008.igem.org/Team:Edinburgh" title="Home"><span>Home</span></a></li>
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<li><a href="https://2008.igem.org/Team:Edinburgh/Project" title="Project" rel="dropmenu1_a"><span>The Project</span></a></li>
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<li><a href="https://2008.igem.org/Team:Edinburgh/Team" title="Team" ><span>The Team</span></a></li>
+
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<li><a href="http://partsregistry.org/cgi/partsdb/pgroup.cgi?pgroup=iGEM2008&group=Edinburgh" title="Project" rel="dropmenu1_a"><span>BioBrick Parts</span></a></li>
+
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<li><a href="https://2008.igem.org/Team:Edinburgh/Modeling" title="Modelling" rel="dropmenu2_a"><span>Modelling</span></a></li>
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<li><a href="https://2008.igem.org/Team:Edinburgh/Notebook" title="Notebook"><span>Notebook</span></a></li>
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</ul>
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</div>
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<div class="ddcolortabsline">&nbsp;</div>
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-
<div id="dropmenu1_a" class="dropmenudiv_a">
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<a href="https://2008.igem.org/Team:Edinburgh/Team">Overview</a>
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<a href="https://2008.igem.org/Team:Edinburgh/Team">Step1</a>
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-
<a href="https://2008.igem.org/Team:Edinburgh/Team">Step2</a>
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</div>
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+
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'''P1:''' ''dxs'' from ''Eschaerichia coli'' JM109 (or K12?)<br />
+
-
'''P2:''' ''appY'' from ''E. coli'' JM109 (or K12?)<br />
+
-
'''P3:''' ''glgC'' from ''E. coli'' JM109 (or K12?)<br />
+
-
'''P4:''' fusion PCR for BABEL1+''glgC''<br />
+
-
'''P5:''' fusion PCR for BABEL2+''glgC''<br />
+
-
'''P6:''' mutagenic PCR to remove EcoRI site 1 from ''glgC''<br />
+
-
'''P7:''' mutagenic PCR to remove EcoRI site 2 from ''glgC''<br />
+
-
'''P8:''' ''crtB'' (from ''Pantoea ananatis'' cells)<br />
+
-
'''P9:''' ''crtI'' (from Douglas's maxiprep of the mutated ''crtIB'' plasmid)<br />
+
-
'''P10:''' ''crtY'' (from ''P. ananatis'' cells). Failed.<br />
+
-
'''P11:''' fusion PCR for rbs+''dxs''. Failed.<br />
+
-
'''P12:''' repeat fusion PCR for rbs+''dxs'', using L11 and primers rbs2fclon1+pSB1A2insr1.<br />
+
-
'''P13 and P14:''' MABEL mutation of site 1 on ''glgC'' mutant clones M19 and M22.<br />
+
-
'''P15:''' fusion PCR for rbs+''appY''<br />
+
-
'''P16, P17, P18 and P19:''' first attempts at ''cenA'', ''cenB'', ''cenC'' and ''cex''.<br />
+
-
'''P20, P21, P22 and P23:''' second attempts at ''cenA'', ''cenB'', ''cenC'' and ''cex''.<br />
+
-
'''P24, P25:''' repeat PCR for ''cenA'' and ''cex'' using Pfu. Failed.<br />
+
-
'''P26:''' Positive control PCR with primers fd1 and rd1 to amplify 16S rRNA gene ''rrnB'' from ''Cellulomonas fimi''.<br />
+
-
'''P27:''' ''crtY'' from ''P. ananatis'' cells. - Failed<br />
+
-
'''P28, P29:''' ''crtB'' and ''crtI'' from L18 and L19.<br />
+
-
'''P30:''' Repeat positive control ''rrnB'' from ''C. fimi'', annealing 1 minute.<br />
+
'''P31:''' pZntA promoter<br />
'''P31:''' pZntA promoter<br />
-
'''P32-P35:''' repeat PCR for ''cenA'', ''cenB'', ''cenC'' and ''cex'', annealing 1 minute. Failed.<br />
+
'''P32-P35:''' Repeat PCR of ''cenA'', ''cenB'', ''cenC'' and ''cex'', annealing 1 minute. (24.07.08: AM) - Failed<br />
-
'''P36:''' M43 (''glgC''-mut1,2) with primers glgCf2/glgCr2 (25.07.08: AM)<br />
+
'''P36:''' M43 (''glgC''-mut1,2) with primers glgCf2/glgCr2. (25.07.08: AM)<br />
'''P37:''' ''crtY'' from ''P. ananatis''. (25.07.08: AM) - Failed<br />
'''P37:''' ''crtY'' from ''P. ananatis''. (25.07.08: AM) - Failed<br />
-
'''P38~P41:''' ''cenA'', ''cenB'', ''cenC'' and ''cex'' from heat-killed cell suspension.<br />
+
'''P38-P41:''' ''cenA'', ''cenB'', ''cenC'' and ''cex'' from heat-killed cell suspension. (28.07.08: AM)<br />
-
'''P42~P45:''' ''cenA'', ''cenB'', ''cenC'' and ''cex'' from 'impure' DNA solution.<br />
+
'''P42-P45:''' ''cenA'', ''cenB'', ''cenC'' and ''cex'' from 'impure' DNA solution. (28.07.08: AM)<br />
-
'''P46~P47:''' ''cenA'' and ''cex'' from 'impure' DNA solution, annealing 65C. Failed.<br />
+
'''P46-P47:''' ''cenA'' and ''cex'' from 'impure' DNA solution, annealing 65C. (20.07.08: AM) - Failed<br />
-
'''P48:''' ''crtY'' (new primer mixture) (previously P38a) (30.07.08: CF) - Failed<br />
+
'''P48:''' ''crtY'' (new primer mixture) (30.07.08: CF) - Failed<br />
-
'''P49:''' Recreation of P12 (rbs+''dxs'') (previously P39a) (30.07.08: CF)<br />
+
'''P49:''' Recreation of P12 (rbs+''dxs'') (30.07.08: CF)<br />
-
'''P50:''' third mutagenesis of ''glgc''-mut1,2 (04.08.08: YAN)<br />
+
'''P50:''' Third mutagenesis of ''glgC''-mut1,2 by MABEL (04.08.08: Yan)<br />
-
'''P51:''' pCstA from ''E. coli'' cells (06.08.08: CF) - Failed<br />
+
'''P51:''' P''cstA'' from ''E. coli'' cells. (06.08.08: CF) - Failed<br />
-
'''P52:''' ''cenA'' from heat killed ''C. fimi'' (07/08/08: YAN, AM) - Failed<br />
+
'''P52:''' ''cenA'' from heat killed ''C. fimi''. (07.08.08: Yan, AM) - Failed<br />
-
'''P53:''' ''cex'' from heat killed ''C. fimi'' (07/08/08: YAN, AM) - Failed<br />
+
'''P53:''' ''cex'' from heat killed ''C. fimi''. (07.08.08: Yan, AM) - Failed<br />
-
'''P54:''' pCstA from ''E. coli'' cells - Purified (07.08.08: CF)<br />
+
'''P54:''' P''cstA'' from ''E. coli'' cells (07.08.08: CF)<br />
 +
'''P55:''' ''cenA'' performed by KOD. (08.08.08: Yan)<br />
 +
'''P56:''' ''cenA'' performed by velocity. (08.08.08: Yan)<br />
 +
'''P57:''' ''cex'' performed by KOD. (08.08.08: Yan)<br />
 +
'''P58:''' ''cex'' performed by Velocity. (08.08.08: Yan)<br />
 +
'''P59:''' pSB1A2+''crtY'' (09.08.08: CF)<br />
 +
'''P60:''' pSB1A2+rbs+''crtY'' (09.08.08: CF)<br />
 +
'''P61:''' 16s rRNA ''rrnB'' from ''C. fimi'' genomic DNA. (10.08.08: CF) - successful<br />
 +
'''P62:''' ''cenA'' from ''C. fimi'' genomic DNA. (10.08.08: CF) - Failed<br />
 +
'''P63:''' ''cex'' from ''C. fimi'' genomic DNA. (10.08.08: CF) - Failed<br />
 +
'''P64:''' ''cex'' from ''C. fimi'' genomic DNA, with 10µl 50% glycerol, annealing 60°C. (11.08.08: AM) - Succesful<br />
 +
'''P65:''' ''cenA'' from ''C. fimi'' genomic DNA, w/ glycerol, annealing 56°C/20s. Success (12.08.08: AM)<br />
 +
'''P66:''' ''SU1'' (12.08.08: CF)<br />
 +
'''P67:''' ''ISO2'' (ISA2) (12.08.08: CF)<br />
 +
'''P68:''' ''cenB'' from ''C. fimi'' genomic DNA. Failed (13.08.08: AM)<br />
 +
'''P69:''' ''cenC'' from ''C. fimi'' genomic DNA. Failed (13.08.08: AM)<br />
 +
'''P70:''' M43 (''glgC'' mut 1+2). Failed (14.08.08: AM)<br />
 +
'''P71:''' M120 (''glgC'' mut 1+2+3). Successful (14.08.08: AM)<br />
 +
'''P71A:''' Repeat M43 (''glgC'' mut 1+2). Succeessful (15.08.08: AM)<br />
 +
'''P72:''' Repeat M120 (''glgC'' mut 1+2+3). Successful (15.08.08: AM)<br />
 +
'''P73~P77:''' ''rrnB'' from ''C. fimi'' genomic DNA purified on 14.08.08. P74 possibly successful (15.08.08: AM)<br />
 +
'''P78A:''' ''rrnB'' from original ''C. fimi'' genomic DNA as positive control. Failed (15.08.08: AM)<br />
 +
'''P78:''' SOB2-''glgC'' mut 1+2 from L45 (19.08.08: AM)<br />
 +
'''P79:''' SOB2-''glgC'' mut 1+2+3 from L46 (19.08.08: AM)<br />
 +
'''P80:''' SOB2-''glgC'' mut 1+2+3 from L47 (19.08.08: AM)<br />
 +
'''P81:''' SOB2-rbs-''glgC'' mut 1+2 from L45 (19.08.08: AM)<br />
 +
'''P82:''' SOB2-rbs-''glgC'' mut 1+2+3 from L46 (19.08.08: AM)<br />
 +
'''P83:''' SOB2-rbs-''glgC'' mut 1+2+3 from L47 (19.08.08: AM)<br />
 +
'''P84:''' ''SU1'' (ISA1) from X11 (20.08.08: AM)<br />
 +
'''P85:''' ''ISO2'' (ISA2) from X12 (20.08.08: AM)<br />
 +
'''P86:''' ''SU1'' (ISA1) from X11, annealing 62°C (21.08.08: AM)<br/>
 +
'''P87:''' ''ISO2'' (ISA2) from X12, annealing 62°C (21.08.08: AM)<br/>
 +
'''P88:''' ''SU1'' (ISA1) from X11, annealing 60°C and glycerol (25.08.08: YAN)<br/>
 +
'''P89:''' ''ISO2'' (ISA2) from X12, annealing 60°C and glycerol (25.08.08: YAN)<br/>
 +
'''P90:''' CHU2268 ''bglX'' - beta-glucosidase from cytophaga, annealing 55°C, extension 50s (26.08.08: YAN)<br/>
 +
'''P91:''' Fusion PCR of P88 and SOB2 ligation products using Forward primer zm1 and Reverse primer sob r1.(01.09.08:YAN)<br/>
 +
'''P92:''' Fusion PCR of P88 and SOB2 ligation products using Forward primer zm1 and Reverse primer sob.rbs.(01.09.08:YAN)<br/>
 +
'''P93:''' Fusion PCR of P89 and SOB2 ligation products using Forward primer zm2 and Reverse primer sob r1.(01.09.08:YAN)<br/>
 +
'''P94:''' Fusion PCR of P89 and SOB2 ligation products using Forward primer zm2 and Reverse primer sob.rbs.(01.09.08:YAN)<br/>
 +
'''P95:''' Site-directed mutagenesis of ''cex'', failed. (05.09.08: YAN)<br/>
 +
'''P96:''' Repeat of Site-directed mutagenesis of ''cex'' (11.09.08: YAN)<br/>
 +
'''P99''' PCR for addition of rbs to ''glgC'' (CF, 24-9-8; OK)<br/>
 +
'''P100''' PCR for affition of rbs to ''glgC16'' (CF, 24-9-8; OK)<br/>
 +
'''P101''' PCR for addition of rbs to ''cex'' (CF, 4-10-8; looked OK but product later turned out to be wrong)<br/>
 +
'''P102''' PCR for addition of rbs to ''cenA'' (CF, 4-10-8; looked OK but product later turned out to be wrong)<br/>
 +
'''P105''' PCR of ''bglX'' with complete suffix (from ligation L74) to allow cloning EcoRI/PstI (CF, 9-10-8, OK)<br/>
 +
'''P106''' mutagenic MABEL PCR to remove EcoRI site from ''SU1''. Failed. (CF)<br/>
 +
'''P107''' repeat P106 with extended denaturation time and 10% v/v glucose: worked (CF, 10-10-8)<br/>
 +
'''P108''' mutagenic MABEL PCR to remove EcoRI site from ''ISO2''. Extended denaaturation time but no glycerol. Failed. (CF, 11-10-8)<br/>
 +
'''P109''' as P108 but with 10% v/v glycerol. Worked. (CF, 11-10-8)<br/>
 +
'''P110''' repeat P101 (rbs+''cex''). Extended denaturation and 10% v/v glycerol. Worked. (CF, 22-10-8)<br/>
 +
'''P111''' repeat P102 (rbs+''cenA''). Extended denaturation and 10% v/v glycerol. Worked. (CF, 22-10-8)<br/>
 +
'''P112''' PCR for addition of rbs to ''bglX''. Worked. (CF, 23-10-8)<br/>
 +
'''P113''' Fusion PCR on ligation L103 to make ''dxs-crtEBI''. Worked. (CF, 26-10-8)<br/>

Latest revision as of 23:56, 29 October 2008

< Back to Notebook

PCR Products

P1: dxs from Escherichia coli JM109. (25.06.08)
P2: appY from E. coli JM109. (25.06.08)
P3: glgC from E. coli JM109. (25.06.08)
P4: Fusion PCR for BABEL1+glgC. (01.07.08)
P5: Fusion PCR for BABEL2+glgC. (01.07.08)
P6: Mutagenic PCR to remove EcoRI site 1 from glgC (M11). (04.07.08)
P7: Mutagenic PCR to remove EcoRI site 2 from glgC (M11). (04.07.08)
P8: crtB (from Pantoea ananatis cells). (08.07.08)
P9: crtI (from Douglas's maxiprep of the mutated crtIB plasmid). (08.07.08)
P10: crtY (from P. ananatis cells). Failed. (08.07.08)
P11: Fusion PCR of rbs+dxs. Failed. (10.07.08)
P12: Repeat fusion PCR of rbs+dxs, using L11 and primers rbs2fclon1+pSB1A2insr1. (13.07.08)
P13-P14: MABEL mutation of site 1 on glgC-mut2 clones M19 and M22. (14.07.08)
P15: Rusion PCR for rbs+appY using L15 as a template. (15.07.08)
P16-P19: First attempts at cenA, cenB, cenC and cex. (17.07.08) - Failed
P20-P23: Second attempts at cenA, cenB, cenC and cex. (18.07.08) - Failed
P24-P25: Repeat PCR for cenA and cex using Pfu. (19.07.08) - Failed
P26: Positive control PCR with primers fd1 and rd1 to amplify 16S rRNA gene rrnB from C. fimi. (22.07.08: AM) - Failed
P27: crtY from P. ananatis cells. (23.07.08: AM, Yan, OG) - Failed
P28: Fusion PCR of rbs+crtB from L18. (23.07.08: AM, Yan, OG)
P29: Fusion PCR of rbs+crtI from L19. (23.07.08: AM, Yan, OG)
P30: Repeat positive control of rrnB from C. fimi, annealing 1 minute. (23.07.08: AM)
P31: pZntA promoter
P32-P35: Repeat PCR of cenA, cenB, cenC and cex, annealing 1 minute. (24.07.08: AM) - Failed
P36: M43 (glgC-mut1,2) with primers glgCf2/glgCr2. (25.07.08: AM)
P37: crtY from P. ananatis. (25.07.08: AM) - Failed
P38-P41: cenA, cenB, cenC and cex from heat-killed cell suspension. (28.07.08: AM)
P42-P45: cenA, cenB, cenC and cex from 'impure' DNA solution. (28.07.08: AM)
P46-P47: cenA and cex from 'impure' DNA solution, annealing 65C. (20.07.08: AM) - Failed
P48: crtY (new primer mixture) (30.07.08: CF) - Failed
P49: Recreation of P12 (rbs+dxs) (30.07.08: CF)
P50: Third mutagenesis of glgC-mut1,2 by MABEL (04.08.08: Yan)
P51: PcstA from E. coli cells. (06.08.08: CF) - Failed
P52: cenA from heat killed C. fimi. (07.08.08: Yan, AM) - Failed
P53: cex from heat killed C. fimi. (07.08.08: Yan, AM) - Failed
P54: PcstA from E. coli cells (07.08.08: CF)
P55: cenA performed by KOD. (08.08.08: Yan)
P56: cenA performed by velocity. (08.08.08: Yan)
P57: cex performed by KOD. (08.08.08: Yan)
P58: cex performed by Velocity. (08.08.08: Yan)
P59: pSB1A2+crtY (09.08.08: CF)
P60: pSB1A2+rbs+crtY (09.08.08: CF)
P61: 16s rRNA rrnB from C. fimi genomic DNA. (10.08.08: CF) - successful
P62: cenA from C. fimi genomic DNA. (10.08.08: CF) - Failed
P63: cex from C. fimi genomic DNA. (10.08.08: CF) - Failed
P64: cex from C. fimi genomic DNA, with 10µl 50% glycerol, annealing 60°C. (11.08.08: AM) - Succesful
P65: cenA from C. fimi genomic DNA, w/ glycerol, annealing 56°C/20s. Success (12.08.08: AM)
P66: SU1 (12.08.08: CF)
P67: ISO2 (ISA2) (12.08.08: CF)
P68: cenB from C. fimi genomic DNA. Failed (13.08.08: AM)
P69: cenC from C. fimi genomic DNA. Failed (13.08.08: AM)
P70: M43 (glgC mut 1+2). Failed (14.08.08: AM)
P71: M120 (glgC mut 1+2+3). Successful (14.08.08: AM)
P71A: Repeat M43 (glgC mut 1+2). Succeessful (15.08.08: AM)
P72: Repeat M120 (glgC mut 1+2+3). Successful (15.08.08: AM)
P73~P77: rrnB from C. fimi genomic DNA purified on 14.08.08. P74 possibly successful (15.08.08: AM)
P78A: rrnB from original C. fimi genomic DNA as positive control. Failed (15.08.08: AM)
P78: SOB2-glgC mut 1+2 from L45 (19.08.08: AM)
P79: SOB2-glgC mut 1+2+3 from L46 (19.08.08: AM)
P80: SOB2-glgC mut 1+2+3 from L47 (19.08.08: AM)
P81: SOB2-rbs-glgC mut 1+2 from L45 (19.08.08: AM)
P82: SOB2-rbs-glgC mut 1+2+3 from L46 (19.08.08: AM)
P83: SOB2-rbs-glgC mut 1+2+3 from L47 (19.08.08: AM)
P84: SU1 (ISA1) from X11 (20.08.08: AM)
P85: ISO2 (ISA2) from X12 (20.08.08: AM)
P86: SU1 (ISA1) from X11, annealing 62°C (21.08.08: AM)
P87: ISO2 (ISA2) from X12, annealing 62°C (21.08.08: AM)
P88: SU1 (ISA1) from X11, annealing 60°C and glycerol (25.08.08: YAN)
P89: ISO2 (ISA2) from X12, annealing 60°C and glycerol (25.08.08: YAN)
P90: CHU2268 bglX - beta-glucosidase from cytophaga, annealing 55°C, extension 50s (26.08.08: YAN)
P91: Fusion PCR of P88 and SOB2 ligation products using Forward primer zm1 and Reverse primer sob r1.(01.09.08:YAN)
P92: Fusion PCR of P88 and SOB2 ligation products using Forward primer zm1 and Reverse primer sob.rbs.(01.09.08:YAN)
P93: Fusion PCR of P89 and SOB2 ligation products using Forward primer zm2 and Reverse primer sob r1.(01.09.08:YAN)
P94: Fusion PCR of P89 and SOB2 ligation products using Forward primer zm2 and Reverse primer sob.rbs.(01.09.08:YAN)
P95: Site-directed mutagenesis of cex, failed. (05.09.08: YAN)
P96: Repeat of Site-directed mutagenesis of cex (11.09.08: YAN)
P99 PCR for addition of rbs to glgC (CF, 24-9-8; OK)
P100 PCR for affition of rbs to glgC16 (CF, 24-9-8; OK)
P101 PCR for addition of rbs to cex (CF, 4-10-8; looked OK but product later turned out to be wrong)
P102 PCR for addition of rbs to cenA (CF, 4-10-8; looked OK but product later turned out to be wrong)
P105 PCR of bglX with complete suffix (from ligation L74) to allow cloning EcoRI/PstI (CF, 9-10-8, OK)
P106 mutagenic MABEL PCR to remove EcoRI site from SU1. Failed. (CF)
P107 repeat P106 with extended denaturation time and 10% v/v glucose: worked (CF, 10-10-8)
P108 mutagenic MABEL PCR to remove EcoRI site from ISO2. Extended denaaturation time but no glycerol. Failed. (CF, 11-10-8)
P109 as P108 but with 10% v/v glycerol. Worked. (CF, 11-10-8)
P110 repeat P101 (rbs+cex). Extended denaturation and 10% v/v glycerol. Worked. (CF, 22-10-8)
P111 repeat P102 (rbs+cenA). Extended denaturation and 10% v/v glycerol. Worked. (CF, 22-10-8)
P112 PCR for addition of rbs to bglX. Worked. (CF, 23-10-8)
P113 Fusion PCR on ligation L103 to make dxs-crtEBI. Worked. (CF, 26-10-8)

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