Difference between revisions of "Part:BBa K2350022"

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pPIGBACK-PrbcL-CrtZ

Part description

Zeaxanthin belongs to carotenoid family and is widely found in the nature. It is also a natural color making corns, carrots and marigolds yellow. Moreover, zeaxanthin is an essential nutrient substance to human’s eyes, and some healthy supplements are made of it. Most of green plants produce zeaxanthin as an intermediate in carotenoid pathway. However, some cyanobacteria lack some genes and cannot produce zeaxanthin, such as Synechococcus elongatus PCC 7942. PCC7942 lacks only one gene making zeaxanthin, that is beta-carotene hydroxylase (CrtZ). To make Synechococcus elongatus PCC 7942 produce zeaxanthin, we construct a plasmid BBa_K2320022 under the control of PrbcL. After the expression of CrtZ, PCC 7942 can then be yellow.

And the crtZ what we use was a part released in iGEM (BBa_I742158) .We have successfully construct this part on our special design backbone pPIGBACK so that it can express in our microalgae and result in yellow microalgae.

Details

1. We studied Professor Chuan-Hsiung Chang’s paper(Energy Environ. Sci., 2012, 5, 8318: Enhancing CO2 bio-mitigation by genetic engineering of cyanobacteria) and decided to construct pigment plasmid with the same promotor. The natural ribosome binding site is also referred to it.

2. The intrinsic promoter of Rubisco large subunit (PrbcL) can overexpress foreign genes in the cyanobacteria. Many plants’ protens in photosynthesis are under regulation of PrbcL. And the high activity to express foreign genes has been proven.

3. CrtZ from Pantoea ananatis is a coding sequence of igem released part (BBa_I742158). It can lead to zeaxanthin and astaxanthin. However, the wild type Synechococcus elongatus PCC 7942 lacks of it and cannot make zeaxanthin naturally.

Result

The right one of Figure 1 is wild type Synechococcus elongatus PCC 7942, the left one was transformant with BBa_K2320022. Obviously, the left one was more yellow than the right one. It proved that CrtZ was successfully transformed to PCC7942 and lead to zeaxanthin. See Figure 1.

Figure 1

Figure 2 is pPIGBACK-CrtZ transformants electrophoresis result. C1~C20 represents the pPIGBACK-CrtZ transformant clone 1 to clone 20, and M represnets 1 kb marker. Transformation efficiency of pPIGBACK-CrtZ is 11.4 transformants per μg DNA, and correctness is 52% (10/19), which is quite efficient because the successful rate of gene double-crossingover homologous recombination is low. See Figure 2.

Figure 2

Figure 3 is cell number, and Figure 4 is the starch content. See Figure 3 and Figure 4.

Figure 3

Figure 4

Figure 5 is starch content per cell, and Figure 6 is delta starch content compared with days. In Figure 6, the starch content change per cell of transformants are more than wild type, and proved that photosynthesis of some transformants were comparable to or more efficient than wild type. See Figure 5 and Figure 6.

Fifure 5

Figure 6

pPIGBACK-PrbcL-CrtZ