Revision as of 07:38, 22 October 2020

AnAmyA Starch degradation

EXP, AnAmyA, XPR2t part will be digested by BsaI and then assembled as the module 2 through the T4 ligase. The module 2 and Leu selection marker will be digested by SapI and then assembled as “EXP-AnAmyA -XPR2t-Leu” expression cassette through the T4 ligase. The cassette can be transformed into the Yarrowia lipolytica plotoplast and integrated into the genome for AnAmyA efficient expression.

Sequence and Features

Usage and Biology

Yarrowia lipolytica use starch as sole carbon sources much slowly when the AnAmyA is expressed successfully, which means the AnGlu has the limited ability to degrade the starch efficiently.

1.The construction and verification of AnAmyA Expression cassette

We constructed the plasmids according to DESIGN page. There are four parts in our plasmid library: a promoter-EXP (BBa_K3578000), a terminator-XPR2t (BBa_K3578002), expression genes-α-amylase (BBa_K3578003), and the Leu selection marker (BBa_K3578004). By BsaI and SapI IIs enzymes digestion and T4 ligase, we successfully constructed the plasmids which separately carried the AnAmyA expression cassette with Leu selection marker (Figure 1). Then plasmids were linearizd with EcoR I and transformed into Y. lipolytica plotoplast. The AnAmyA expression cassette with Leu selection marker DNA fragment will be randomly integrated into genome loci.

Figure 1 Schematic diagram of plasmid construction process.

By the PCR experiment, 10 strains integrating AnAmyA and Leu expression cassette were picked up for the following experiments. We designed the primers(F/R) to identify the AnAmyA expression cassette. The primer design were shown in the figure 2, and the predicted PCR result is 2736 bp. The electrophoresis results showed that about 3000 bp bands were obtained by using AnAmyA expression cassette as template, the electrophoresis results were consistent with our expectation(Figure 2).

Figure 2 Primer design and agarose gel electrophoresis for plasmid identification.