Difference between revisions of "840:153g:Projects/project24"

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'''Source:''' Biology department of University of Northern Iowa
*Source: Biology department of University of Northern Iowa
'''Media:''' Luria Broth
*Media: Luria Broth
'''Gene:''' Acetyl CoA carboxylase biotin carboxylase (accC)
#Gene: Acetyl CoA carboxylase biotin carboxylase (accC)
'''Accession #:''' NC_011353.1 Region: 4242644..4243993 total base pair- 1350
#Accession no.: NC_011353.1 Region: 4242644..4243993 total base pair- 1350

Revision as of 10:42, 13 September 2012

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Team Members

  • Sanju Timilsina
  • Parul Sirohi

Over expression of E. coli Acetyl- CoA carboxylase (ACC)sub-unit accC in E.coli to enhance fatty acid accumulation for Bio-fuel production”.

  • Source Organism: E. coli 0157:H7

PROJECT DESCRIPTION Our gene of interest is accC gene from E. coli 0157:H7 accC gene is the biotin subunit of ACC enzyme which catalyze the biosynthesis of Malonyl CoA. Malonyl CoA controls the rate of fatty acid (Triacylglycerol) biosynthesis.TAG is the fatty acid i.e. used for the biofuel production.In this experiment we will identify if the overexpression of accC gene in E.coli might enhance the production of TAG. For this process we will chttp://openwetware.org/skins/common/images/button_bold.pnglone our gene of interest in to plasmid pSB1A3 and transform it in host E. coli. We will do SDS-PAGE for detection of protein and thin layer chromatography for the quantification of fatty acids.

  • Source: Biology department of University of Northern Iowa
  • Media: Luria Broth

  1. Gene: Acetyl CoA carboxylase biotin carboxylase (accC)

  1. Accession no.: NC_011353.1 Region: 4242644..4243993 total base pair- 1350

Introns: None because Bacteria does not have any introns.

Bio-brick Compatibility: Compatible

Plasmid used: Vector Plasmid pSB1A3

Promoter used:Part: BBa_J23100 ttgacggctagctcagtcctaggtacagtgctagc

Alternative Promoters: BBa-K206000(PBad): is strong E.coli promoter controlled by L-arabinose inducer and is repressed by AraC.

J23109:RFP-106 tttacagctagctcagtcctagggactgtgctagc (is medium promoter)

PCR primers for accC gene

• 24F_Biofuel1P 5’gaattcgcggccgcttctagagatgctggataaaattgttattgccaaccgc 3’

• 24RP_Biofuel2S 5’tactagtagcggccgctgcagcgagttttttctccagatagtggatgttagtgc3’

• 24F_Biofuel1 5’ atgctggataaaattgttattgccaaccgc 3’

• 24RP_Biofuel2 5’ cgagttttttctccagatagtggatgttagtgc3’

'''Steps for project:'''

• Grow the source organism (E. coli)

• DNA extraction from the source (E. coli)

• Electrophoresis to check desired DNA segment (bp)

• Primer designing

• Multiplication of gene of interest by PCR

• Electrophorosis

• Digestion of Plasmid and gene by restriction enzymes

• Ligation of accC gene in plasmid vector (pSB1A3)

• Transformation of vector plasmid into host organism E. coli

• Cloning of cells in a LB media

• Selection for recombinant DNA colonies by antibiotic selective media (LB+ ampicillin)

• Inoculation of E.coli in biomass

• Testing of protein Acetyl CoA carboxylase biotin carboxylage by SDS-PAGE and fatty acid by thin layer chromatography


• Magnuson, K., Jackowski, S., Rock, C.O., and Cronan, J.E.(1993).Regulation of fatty acid biosynthesis in Escherichia coli. Microbial Rev.57(3):522

• Noemie, M. D., Parisien, A., Wang, B., Lan, C., ( 2009). Enhancement of lipid production using biochemical, genetic and transcription factor engineering approaches. Journal of biotechnology, 141 (2009) 31-41





Fuel_it_up_FINAL_Slides_-_Copy_corrected_after_presentation.pptx (file)

Important Results and Milestones

  • keep track of your most important results and refer to the corresponding page in your notebook
  • upload important pictures (don't forget to label them! Powerpoint is very convenient). Remember: these will become quite handy later in your summary report or final presentation. If you do label and upload the pictures as soon as you got them, your summary report can be written much more effortlessly (do you usually procrastinate? This is chance to do some work before hand that frees you up for finals week).

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