Design and Construction of Alk-Selector

Firstly, we will design a new device Alk-Selector. Although Alk-Sensor can also be regarded as a selector, we don’t want to select just by our eyes which is a tough work. Instead, the special function of antibiotic resistant gene will help us select out the gene with better property automatically in the condition of antibiotic pressure.

So based on the construction of Alk-Sensor, we replaced the RFP reporter with tetracycline resistant gene TetA which is a transporter to pump tetracycline outward the cell. Other components of the Alk-Selector are same to Alk-Sensor. The final construction of Alk-Selector and its working mechanism can be seen in Figure 1. The alkane biosynthesis module expresses NPDC and AAR to produce alkane in E. coli, and then the alkane can activate the expression of tetA through AlkR-PalkM system, and the transporter TetA will give tetracycline resistance to E. coli and make it survive in the environment with tetracycline.

Figure 1. Working mechanism of Alk-Selector. Cells cultured in 3ml M9 medium with 12ug/ml tetracycline. When alkanes induce the Alk-Selector, protein tetA will express, and make cells survive in the environment of tetracycline.

Characterization of Alk-Selector

To verify that Alk-Selector will generate more tetracycline resistance when more alkanes are produced, we cotransformed the Alk-Selector and an alkane producing module to the E. coli BL21. The control strain just had Alk-Selector. These two strains were cultured in M9 medium with 12ug/ml tetracycline. After 48h, we can find the growth of strain with alkane producing module was higher than the control just as Figure 2 showed.

It proved that our Alk-Selector can work.

Figure 2. Construction scheme of two Alk-Selector strains.Strain one contains alkane producer part(left),the other contains none-producer part (right) .And the result is upon the structure. The none-producer strain grew much slower than alkane producing one.

Library Construction

For library construction, we reconstructed the alkane producing module of low productivity by adding restriction site BamHI and SacI at the two ends of gene NPDC for library construction. The workflow of the library construction is showed in Figure 3.

Figure 3. The workflow of the library construction.

We amplified NPDC by error-prone PCR, and ligand on the plasmid. The product of ligation is transformed into competent cell with high efficiency, to get the library of alkane producing module. Because of the limitation of time, the size of the library is just 20,000. Just as Figure 4 shows, every plate had about 3000 colonies, more than 90% colonies were amplified fragments with correct length (~2000bp) by colony PCR(Figure 5), and 8 plates like this had been made. Then, the colonies were washed out and got together and then whole plasmids were extracted from it to get the amplified plasmid library of alkane producing module. This library was later transformed into the E. coli BL21 containing Alk-Selector.

Figure 4. Plate colony count result of library construction strains, with about 3000 colonies on the plate.

Figure 5. Colony PCR result of library construction strains. More than 90% colonies were amplified fragments with correct length (~2000bp)

Process of Selection and Analysis

The whole process of selection has been showed in Figure6. The amplified plasmid library was transformed to E. coli with Alk-Selector. To guarantee this library’s diversity, we think that the number of the strain which has successfully taken in the alkane producing module was at least 60,000. To verify this requirement, all the strains will be plated on the M9 solid medium, and the numbers of the colonies will be estimated. As Figure 6 showed that the number of 1/10 of all transformants is about 6500 which has satisfied the requirement. At the same time, the strains that didn’t take in the plasmid would eliminate under the pressure of antibiotic in this process. Then, all the colonies were washed out by M9 medium with antibiotics of proper concentration. The mix culture was inoculated into M9 medium with 12ug/ml tetracycline by 1:1000 for selection. For the control group, this culture was inoculated in the M9 medium without tetracycline. After fermentation for about 12 hours, E. coli began to grow very slowly, and after 36h, the OD600 of culture beyond 2.0 which was enough to analyze.

Figure 6. Selection and analysis process of the library with the help of Alk-Selector.

Because of the high copy number of Alk-Selector, directly separation of the colonies that survived during the selection process failed in the sequencing, so we extracted whole plasmid from the culture and retransformed to the E. coli without any module to discard the plasmid of Alk-Selector. The colonies will be picked up and sent for sequencing. After aligning the sequence, we can find the key animo acid which influences the function of the enzyme, and get the better module of alkane producing.

Result

We picked 50 colonies for sequencing. Limited by the size of the library, only 2 mutation has been found which is F133Y and E144G. Figure 7 and Figure 8 shows this result. About 80% strains contained both of the mutation (No strain from control experiment is enriched). Among two of the mutation, E144G is just nearby the key amino residue E145 which is responsible to stabilize the iron ions of the active center, so this mutation may influence the activity of the enzyme. F133Y is far away to the active center, but may affect the entrance of the substrate to the pocket. Limited by the time, we didn’t test the function of the alkane producing module.

Anyway, we successfully finished our selection process from a library under the help of Alk-Selector. And we had proved that this favorite biobrick can work.

Figure 7. 3D structure of enzyme NPDC with 2 mutation sites marked up: F133Y and E144G, and E144G is just nearby the key amino residue E145.

Figure 8. Gene sequences of NPDC and error NPDC, with 2 mutation sites:F133Y and E144G.