Melbourne/Plan/Blue Photosensor

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Preliminaries

  1. Usefull links (restriction enzymes) (Software)<open wetware primer design>

<more primer design>

  1. Sequences:
    1. Ncbi genebank AF053765 (pNL26 7371bp) (pNL29 6036bp) [http://www.ncbi.nlm.nih.gov/entrez/viewer.fcgi?db=nuccore&id=3089519| (original source)]

(FASTA seq.)

    1. pBluescriptIIKS+ [http://www.stratagene.com/products/displayProduct.aspx?pid=267 (stratagene) ]

[http://www.stratagene.com/vectors/sequences/pbl2ksp_s.txt (sequence) ]

[http://www.stratagene.com/vectors/restriction_sites/pbl2ksp_r.txt (restriction map) ]

[http://www.stratagene.com/vectors/maps/pdf/pBluescript%20II%20KS+_%20webpg.pdf (map) ]

[http://www.stratagene.com/manuals/212205.pdf (Manual)]

    2. pNL26 Plasmid with insert: (seq 10318bp) [[Melbourne/cannon plasmid

pNL26 res map| (res map)]] (digests) [[Melbourne cannon plasmid

pNL26 rev compl seq|(reverse complement)]]

      1. pNL26 insert PstI--HindIII:(pNL26 7371bp)
    2. pNL29 Plasmid with insert: (seq 8983bp) [[Melbourne/cannon plasmid

pNL29 res map| (res map)]] (digests) [[Melbourne cannon plasmid

pNL29 rev compl seq|(reverse complement)]]

      1. pNL29 insert PstI--HindIII:(pNL29 6036bp)
    2. Frame arrangement for Biobrick protein expression.
    3. Biobrick expression plasmid system.
    4. Basic biobrick primers pNL26F,pNL29F,pNLR, GvpAF, GvpBF, GvpUR -> 6 combinations
      1. design primers
      2. create registery parts
    5. pNL26 only genes biobrick pcr primers: GvpA,GvpP,GvpQ -> 6 protein generators.
    6. pNL29 biobrick primers: GvpB,gvpR,GvpN,GvpF,GvpG,GvpL,GvpS,GvpK,gvpJ,GvpT,GvpU
      1. design forward and reverse primers for each except gvpUF, GvpBR which will definately not be required.
      2. create registery parts
  2. Other investigations
    1. Locate putative transcription terminators.
    2. Locate putative ribosome binding sites.
    3. Locate putative regulation sequences/ promotors.
    4. Confirm putative genes.
    5. Blast search homology of each putative ORF & gene.
    6. Produce phylogenic maps of Gvps.

Steps:

  1. Recovery of genes: (2 days)
    1. Recover the plasmid from paper provided into solution.(method)
    2. Transform E.Coli strain DH5alpha. Screen with Amp 100ug/ml (as per ref.)(electroporation & heatshock)
    3. pick 3 colonies of each
    4. Overnight Culture x9(6 above and 3 form agar block provided)
    5. Miniprep
    6. Produce glycerol stocks
    7. Confirm presence in recovered sample using digest.(HindIII)
    8. ->Established Supply of Plasmid
  2. Induce translation overnight 37deg with IPTG in 100ml plates (method)(2days)
    1. Confirm transcription RT-PRC,
    2. Confirm translation (buoyant phenotype method).
    3. Confirm translation (Namarski optics (direct interferance contrast microscopy method).
  3. Removal of four biobrick like restriction sites all in GvpL.
    1. DNA code Usage in Ecoli K12 from http://www.kazusa.or.jp/codon (result)
    2. (Quickchange XL Kit)[http://www.stratagene.com/sdmdesigner/default.aspx (Primer

design program) ] [http://www.stratagene.com/downloads/qc/200521.pdf (Manual)][[Melbourne/GvpL site dirrected

primers|(Primer program output)]] (hand designed primers ordered)

    1. EcoRI [GAATTC] in gvpL (2858)is out of frame [GA G][AAT][TC A]-> [E(glutamate),N(asparagine),S(serine)]
      • Replace with [GA A][AAT][TC A] Glutamate: from [GAG](K12 usage 18%) to [GAA](K12 usage 40%).
    2. PstI [CTGCAG] in gvpL x 3 (2522,2900,3005) each is in frame [CTG][CAG]-> [L(leucine),Q(glutamine)]
      • Replace with [CTG][CAA] Glutamine: [CAG](K12 usage 29%) to [CAA](K12 usage 15%).
    3. XbaI [TCTAGA] (not present)
    4. SpeI [ACTAGT] (not present)
  2. Insertion of biobrick required restriction sites by PCR primer modification.(method)
    1. Design of primers: see: http://www.openwetware.org/wiki/Designing_primers
      1. PREFIX Primer 3cctttctagag5 11 bp adds XbaI
      2. SUFFIX Primer 3tactagtagcggccgctgcagcctt5 25 bp adds (Spe I-Not I-Pst I)
      3. In Frame for expression when combined with Lac promotor.
    2. Primer generation
    3. Plasmid extraction from culture
    4. PCR
    5. Restriction EcoR1 & Spe1
    6. Gel separation
    7. Restriction of standard Library death plasmid EcoR1,Spe1.
    8. Ligation.
    9. Transform host with regulated POPS output
    10. Confirm dna, rna , protein (as for A)

supplementary material for use in experiments

source)]

      • coden pair change: Isoleucine T57C: [ATT](K12 usage 30%) to [ATC](K12 usage 25%).(adds EcoRV)
      • Primer T57AF 5'-ttagcagaagtgattgatcgaatcctcgacaaagggattg-3'
      • Primer T57AR 5'-caatccctttgtcgaggattcgatcaatcacttctgctaa-3'


source)]

      • coden pair change:Glutamine G441A: [CAG](K12 usage 29%) to [CAA](K12 usage 15%).
      • mutation Primer G441AF 5'-aatatgaacgaccagctgcaacgcattgaagagatg-3'
      • mutation Primer G441AR 5'-catctcttcaatgcgttgcagctggtcgttcatatt-3'

(original source)]

      • coden pair change:Glutamine G150A,G183A: [CAG](K12 usage 29%) to [CAA](K12 usage 15%).
      • mutation Primer #1 G150AF: 5'-aaaactgaagggaaactgcaagaaaaagcaaatgaagcgtc-3'
      • mutation Primer #1 G150AR: 5'-gacgcttcatttgctttttcttgcagtttcccttcagtttt-3'
      • mutation Primer #1 G183AF: 5'-atgaagcgtcagaaaaactgcaagaaacaaaagaaaaaaatgccc-3'
      • mutation Primer #1 G183AR: 5'-gggcatttttttcttttgtttcttgcagtttttctgacgcttcat-3'
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