AI Article Synopsis

  • The study aimed to develop a novel gene expression system for producing heterologous proteins using a specific organism, which had previously faced limitations in secretion-type systems.
  • A new vector called pAU5 was created, utilizing a strong promoter and a specialized signal sequence to effectively secrete the α-amylase protein from the organism into the culture supernatant.
  • Results showed that the α-amylase was successfully expressed and secreted in an active form, demonstrating the efficiency of the pAU5 system for protein production.

Article Abstract

Background: () is a potential host for the secretory production of the heterologous proteins. However, to this date few secretion-type gene expression systems in have been developed, which limit applications of in a secretory production of the heterologous proteins.

Objectives: In this study, a novel and efficient general secretory (Sec) pathway-dependent type gene expression system for the production of heterologous proteins was developed in .

Materials And Methods: The synthesized cloning/expression cassette C was assembled into the basic - shuttle vector pAU2, generating the Sec-dependent type gene expression vector pAU5. Subsequently, the applicability of the /pAU5 system was tested using the α-amylase AmyE from as a reporter protein.

Results: The vector pAU5 was successfully constructed. The SDS-PAGE experiment showed the AmyE protein band could be observed in the original culture supernatant of the 14067/pAU5-. The Western blotting experiment showed that the AmyE polypeptide could be detected in the culture supernatant of the 14067/pAU5-, not in the cell lysate of 14067/pAU5-. The α-amylase specific activity of the culture supernatant of 14067/pAU5- was 103.24±7.14 U.mg protein, while no α-amylase activity was detected in the cell homogenate supernatant of 14067/pAU5-. These results demonstrate that the recombinant AmyE was efficiently expressed and completely secreted into the extracellular environmentin an active form in /pAU5 system.

Conclusions: A novel efficient Sec-dependent type gene expression vector pAU5 was constructed in the . The vector pAU5 employs the strong promoter for controlling a constitutive transcription of the target gene, the consensus ribosome binding site (RBS) sequence of to ensure protein translation, and the efficient Sec-type cgR_2070 signal sequence to mediate protein secretion in the The pAU5 system is an efficient expression system for the secretory production of the heterologous proteins.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217267PMC
http://dx.doi.org/10.21859/ijb.1746DOI Listing

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