Team:UST Beijing/Project

Comparison between mouse and human GLO gene locus identified only 6 exons on human genomic DNA. These exons also carry a few nucleotide mutations. These remaining exons include sequences coding for both FAD binding and D-arabinono-1,4-lactone oxidase(ALO) domain of GLO enzyme protein. This evidence indicates that human GLO gene used to be active in the past. Source: Nishikimi M et al JBC (1994) 269:13685-88.

An Alternative hypothesis believes that the losing of GLO gene, production of which catalyze final production of vitamin C, could be advantageous because this Vitamin C (VitC) production is at the expanse of hydrogen peroxide formation[Free Radical Research, July 2005; 39(7): 671–686] and depletion of glutathione. However, some species of birds and bats have regained their capability of vitamin C synthesis after they lost it in the evolution process, which means such capability is still helpful. Another evidence is that GLO gene knock out mice show some disability in environment adaptation [Immune Network 2012;12(1):18-26]. We believe that reactivation of GLO in animal is more likely to be advantageous but the expression rate should be carefully controlled because the overwhelming amount of VitC could interfere the metabolism in cells. Since the promoter and other regulatory sequence of GLO Pseudogene have already lost its original function, new method was needed to determine appropriate expression rate. Considering the function of Vc in Antioxidant, proteorhodopsin as a light driven proton pump was designed and introduced to simulate oxygen species rich environment. Proteorhodopsin, when exposed to light, can contribute greatly to free radical production was used to titration the possible effect of different amount of GLO expression.

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We downloaded the sequences of Glucose oxidase from database and use the CLC sequence viewer to analysis. Comparative promoters of Glucose oxidase from different dietary animals are shown in this picture. The signature sequences conserved can be seen in boxes. The sequences between the black ball and the code ATG are represent exons that are still found in the genome of these species. The code ATG is the initiation of the translation.

A new Biobrick device: Mitochondrial proteorhodopsin (humanized genetic code bias)
Partsregistry submission：
BBa_K603000 (pSB1AC3)
BBa_K603001 (pSB1C3)

As we can see from the pictures taken by fluorescence microscope, transient expression of mitochondrial proteorhodopsin (mPR) and GFP genes in human embryonic kidney cells HEK293 is obviously related to the light exposure. In the dark (None) GFP expression rate is lower than the weak light exposure (weak) . The flow cytometry result also shows that the light exposure increased level of transient GFP expression ( accumulative green fluorescence is intensity 195.84) in HEK293 cells co-transfected with mPR and GFP expression vectors compared with no light exposure (168.23). The culture condition is nutrient-poor, therefore energy harvest from light is positively correlated to GFP expression.

The graph above shows that the amount of surviving cells is related to the change of Vitamin C (VitC) concentration. When the fold of dilution of Vit C is zero , the amount of surviving cells is relatively high (probably due to Vitamin C poor solubility). However, with the growth of fold of dilution, the number of surviving cells declines, because high concentration of VitC makes media acidic which can do harm to cells. When the fold of dilution comes to two, the cells are weakest. When higher than 2 fold of diluton, the VitC contributes the growth of amount of surviving cells. The higher the fold of dilution of VitC before seven, the higher the amount of surviving cells was. After the seven fold of dilution of VitC, the amount of surviving cells will decrease due to too low Vit C concentration.