Part:BBa_K2407303

β-carotene gene

A composite part of three key genes to produce β-carotene which can be expressed in Saccharomyces Cerevisiae.

Introduction

After reviewing the literature, we understand that carotene can be overexpressed in Saccharomyces cerevisiae. Furthermore, carotenoid production levels were higher in strains containing integrated carotenogenic genes. Overexpression of crtYB and crtI from X. dendrorhous was sufficient to enable carotenoid production. crtYB, crtI, and crtE can complete the expression of β-carotene, and the cell is orange.

Components of the Mating switcher

To characterize our Mating Switcher, we built a gene route to switch the expression from RFP to β-carotene. In this route, we combined RFP with TEF-1 promoter. To prevent leaky expression, we choose two kinds of terminators——ADH1 and Ura3‘s. So β-carotene’s expression is controlled by promoter-vox-RFP-Terminators-vox structure. Before the mating-type switch, our yeast presents reddish color due to RFP’s expression. After the Mating Switcher, with the deletion of RFP and terminators flanked by vox locus, β-carotene expresses and the strains take on an orange color. In Saccharomyces cerevisiae, these two colors are easy to distinguish. In this way, we can easily visualize the function of our switcher, as well as measure its efficiency and error rate.

This part was amplified by using the primers indicated by René Verwaal (2007), Some of those primers are:

• crtYB-F CGC GGATCC ATGACGGCTCTCGCATATTAC
• crtYB-R TGCG GTCGAC TTACTGCCCTTCCCATCCGC
• CRTI-F GCG GGATCC ATGGGAAAAGAACAAGATCAGG
• CRTI-R TGCG GTCGAC TCAGAAAGCAAGAACACCAACG
• crtE-F CGC GGATCC ATGGATTACGCGAACATCCTC
• crtE-R TGCG GTCGAC TCACAGAGGGATATCGGCTAG

We designed different promoters in the middle of each carotene genes, and used overlap PCR to combine them together.

Sequence

The part consists of TEF1 promotor, crtE, tTDH3 promotor, crtI, tFBA1 promotor and crtYB. The expression of crtE is controlled by TEF1 promotor, the expression of crtI is controlled by tDH3 promotor,and the expression of crtYB is controlled by tFBA1 promotor.

Theory

Figure 1. the carotenogenic pathway in X. dendrorhous.

crtYB, crtI, and crtE are originate from X. dendrorhous. Just as shown above, the carotenogenic pathway in X. dendrorhous consists of GGPP synthase encoded by crtE, the bifunctional enzyme phytoene synthase and lycopene cyclase encoded by crtYB, and phytoene desaturase encoded by crtI. S. cerevisiae contains a GGPP synthase, encoded by BTS1, which is able to convert FPP into GGPP. HMG1 encodes HMG-CoA reductase, which is the main regulatory point in the ergosterol biosynthetic pathway in many organisms. IPP, isopentenyl diphosphate; DMAP, dimethylallyl diphosphate; GPP, geranyl diphosphate. (René Verwaal, et al, 2007)

Result

We succeeded to integrate this part into the chromosome of Saccharomyces cerevisiae by homologous recombination. With the expression of β-carotene, cell is orange. The result is showed below:

Figure 2. The result of transformation.. The left side of the figure is the original Synthetic Saccharomyces cerevisiae, whose color is white. The orange strain on the right is the bacteria what we obtained.

Sequence and Features

Assembly Compatibility:

• 10
  COMPATIBLE WITH RFC[10]
• 12
  COMPATIBLE WITH RFC[12]
• 21
  INCOMPATIBLE WITH RFC[21]

  Illegal BglII site found at 749
  Illegal BglII site found at 2436
  Illegal XhoI site found at 448
  Illegal XhoI site found at 580
  Illegal XhoI site found at 1399
  
• 23
  COMPATIBLE WITH RFC[23]
• 25
  INCOMPATIBLE WITH RFC[25]

  Illegal AgeI site found at 616
  
• 1000
  INCOMPATIBLE WITH RFC[1000]

  Illegal BsaI site found at 3340
  Illegal BsaI site found at 5695
  Illegal BsaI.rc site found at 176
  Illegal BsaI.rc site found at 6026
  Illegal SapI site found at 2740