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iGEM

iGEM. 8.3.10 - 8.6.10. Arsenic Bioremediation. Possibly finished biobrick for ArsR by adding a RBS and terminator. Will send for sequencing today or Monday.     Do we only send them the forward primer?

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iGEM

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  1. iGEM 8.3.10 - 8.6.10

  2. Arsenic Bioremediation Possibly finished biobrick for ArsR by adding a RBS and terminator. Will send for sequencing today or Monday.     Do we only send them the forward primer? Tried ArsB gradient with increased DMSO concentration, still no luck. Placed order for redesigned primers. We have all the genes we need on plasmids except for ArsB and possibly LamB, we're troubleshooting our verification PCR for contamination.  Received questionable sequencing results from ArsR site directed mutagenesis. Most likely resulted from impure sample.

  3. Expected Sizes: pArsR: ~850 bp LamB: ~1.6 kB

  4.  (-) no template 1 Kb  Ladder ArsR RBS Term. 1 ArsR RBS Term. 2 LamB  F2R 1' LamB  F2R 2' LamB F2R LamB F2R Green ArsR  mut. 2 (-)  no primers Expected Sizes: ArsR RBS Term: 600-700 bp LamB:~1.6 Kb ArsR mut: ~600 bp

  5. Site Directed Mutagenesis: ArsR ArsR Coding Region: ATG TCA TTT CTG TTA CCC ATC CAA TTG TTC AAA ATT CTT GCT GAT GAA ACC CGT CTG GGC ATC GTT TTA CTG CTC AGC GAA CTG GGA GAG TTA TGC GTC TGC GAT CTC TCA CTG CTC TCG ACC AGT CGC AGC CCA AGA TCT CCC GCC ACC TGG CAT TGC TGC GTG AAA GCG GGC TAT TGC TGG ACC GCA AGC AAG GTA AGT GGG TTC ATT ACC GCT TAT CAC CGC ATA TTC CAG CAT GGG CGG CGA AAA TTA TTG ATG AGG CCT GGC GAT GTG AAC AGG AAA AGG TTC AGG CGA TTG TCC GCA ACC TGG CTC GAC AAA ACT GTT CC GGG GAC AGT AAG AAC ATT TGC AGT TAA The goal was to change the Xba cut site AGATCT to AGGTCT. This change coded for the same amino acid with a similar frequency to the AGA  codon. 

  6. Sequencing Results: ArsR Site Directed Mutagenesis Sample 2

  7. Expected Sequence: tgccacctgacgtctaagaaaccattattatcatgacattaacctataaaaataggcgtatcacgaggcagaatttcagataaaaaaaatccttagctttcgctaaggatgatttctggaattcgcggccgcttctagagATGTCATTTCTGTTACCCATCCAATTGTTCAAAATTCTTGCTGATGAAACCCGTCTGGGCATCGTTTTACTGCTCAGCGAACTGGGAGAGTTATGCGTCTGCGATCTCTGCACTGCTCTCGACCAGTCGCAGCCCAAGGTCTCCCGCCACCTGGCATTGCTGCGTGAAAGCGGGCTATTGCTGGACCGCAAGCAAGGTAAGTGGGTTCATTACCGCTTATCACCGCATATTCCAGCATGGGCGGCGAAAATTATTGATGAGGCCTGGCGATGTGAACAGGAAAAGGTTCAGGCGATTGTCCGCAACCTGGCTCGACAAAACTGTTCCGGGGACAGTAAGAACATTTGCAGTTAAtactagtagcggccgctgcaggcttcctcgctcactgactcgctgcgctcggtcgttcggctgcggcgagcggtatcagctcactcaaaggcggtaat ArsR Site Directed Mutagenesis 2:CCTTGCGTCCGTCGAGACGATCGGAGCTAGTCGAGGAGCGAGTTTGCCAGCAACGGATGCTTCTCTTATTAACTGGAATGT TTCTTAGAGTTCCCGGCCCCTTCTTGATGACATTTCTGGCAGACATCCGCCTGTTCCAAATTCCTGTTCAATTAACCCCGC CTGGTCATCAATTTTACTGCTCCCATGAACTGAATATAGTTATGATATCTGCGTATCTCTGCCATGTTACTTTGCCATGTC GTCCACCAAGGTCTCCCGTTTCACTGGCATTGGTGCGGGGAAGCGGGACCTTGCTGGTGCCGACTGGTCGGTAGCTGTGTT CATTACCGCTTATCATAACTCATCCCATTCTGTGAGGCGTAAAATTAATGCCCAAAGCCTGTTTCATGTGAACGAAATATG GATCATGGGATGGTCCACAAACTGGATCTCCAAAACTGTTCCCGGAATCCAAAAATCATTTGTAGTTAATGCTAATGATTT TTTCTATCTGATTCTCCGCTCCCTGACTCGCCTATTTTTATAGGTTAATGTGCATGATAGTAATGGTTTCTCACTACGTCG CGTGGCTCTTTTTATCCACATGTTCGCGGAATCACTATTGGTATATTTTTCTAACTACATGCCAATATGTAGCCGCTAATG AGACAATAACCCTGATAAATGCTTTTTAATATTGCTCCGCCCCCCAGACTAACTTCTCAACATTCCACTCTCACCCTTAAT CCCTTTAATCCCGGCATTGACTATTCCTGACCATGCTCACCCCCCTGCACTCGCCATCGTGCGCTATGCTGATCATACCCT GCCTGTTACCGGATACCTGTTCGCCTTGGATCTTCGGGAAGCGTGGATCTTTCACATATTTCACCCTGAAGAAATCTCACC TCTGAGGAGCACTTTTCAAACCTCGCCTGGGCTGGGGGGCATAATACCCCCCGATTAACCCCACCGCTGAGCATTTCCGGT AACTATACTCTAGTCTCCAAACCGACTTAGGATTGAATACTATCCCGTCTGGCAACAGCATCTTGACACATGGATTGCAGA TCGAGAATGTGCGCGGCGCGTCATAGCTACTGAGAAGATGACGCTCTCAGCTACACGTTACTTCTAGACGACCATCGTATG AGCATCATGCAGCTTAGCTGCATTCATGTCACATCTGGAGGATATGGAAATTCTTCTGATTCGTCGAGACACCGACCCTAG GTAAGC

  8. Gold - Re-ligated golS onto plasmid since sequence homology last time was poor (79% homology) - Possibly have golB on a plasmid, but still need to  do miniprep and digestion  to verify (there were no  bands from the first colony)

  9. Gel extraction: gesABC ges abc

  10. - PCR'ed out GolS promoter and more golT  and gesABC - Working on putting those parts on plasmids, and combining GolS promoter with GFP - Hope to have a fluorescence assay done soon to measure GolS response to gold

  11. PCR from genome of ges works, but can't amplify ges or golT fragments from gel extraction

  12. - Haven't been able to PCR gesABC gel extraction template     (lanes have a "smear" down them)

  13. RNA Decoder We have continued on our digestion/ligation/transformations for the project.  We still need to PCR out EGFP and MicF, but otherwise we have all the parts we need.  This morning we checked on transformants done yesterday and only had 2 of 5 plates growing colonies. When we ran a gel for our digestions of each part, every miniprep has some sequence that is ~6 kB in it. What could that be? Could it be affecting our transformations?

  14. Other Updates    Dip'n Dots Fundraiser went well! Who should we plan on taking to the Jamboree - please fill out an intent to travel form. GAMES camp went well Next Friday will be our last meeting of the summer.  During the semester, we'd like to have meetings one every 2-3 weeks. What days and times work well or don't work? We received donations from Midsci and S.J. Smith, and the tools team has been in contact with Tetravitae about potential sponsorship

  15. Sequencing Results: ArsR Site Directed Mutagenesis Sample 1

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