BBa_K814014

BBa_K814014 Version 1

Component

Source:
http://parts.igem.org/Part:BBa_K814014
Generated By: https://synbiohub.org/public/igem/igem2sbol/1
Created by: George Chao, Misha Patel, Hannah Aho, Molly Swanson, Dana Morrone
Date created: 2012-10-02 11:00:00
Date modified: 2015-05-08 01:13:28

caffeine biosynthetic pathway for yeast



Types
DnaRegion

Roles
engineered_region

Device

Sequences BBa_K814014_sequence (Version 1)

Description

The induction of this novel pathway in S. cerevisiae requires two additional enzymes from Coffea canephora: XMT1 and DXMT1. S. cerevisiae will produce the required metabolic precursors to Xanthosine, where after the XMT1 enzyme from C. canephora will use the substrate to synthesize 7-methylxanthosine. DXMT1 will continue the synthesis by converting to 7-Methylxanthine, where in XMT1 will again convert it to Theobromine. Finally DXMT1 will convert the metabolite to caffeine. Both the XMT1 and DXMT1 genes produce bifunctional enzymes and this particular pathway was chosen so that one less enzyme would be required in the synthesis (compared to three in C. arabica).

This device contains XMT1 and DXMT1 generators designed for yeast. This part can be used for caffeine biosynthesis in yeast.

Notes

The sequences were ordered from IDT as G-Blocks and assembled using overlap-extension PCR to make each part. The parts were then assembled using classic BioBrick technique.

Source

The sequences were generated using a program developed by our team which takes multiple codon-optimized sequences, looks for regions of homology between them, and disrupts these regions by ???de-optimizing??? the region in such a way as to eliminate homology. This is important for developing and assembling yeast BioBrickTM parts in such a way that designed sequences will not undergo homologous recombination.

igem#experience
None
 
igem#sampleStatus
It's complicated
igem#status
Planning
 
synbiohub#ownedBy
user/james
 
synbiohub#ownedBy
user/myers
 
synbiohub#topLevel
BBa_K814014/1