Abstract

Background Saccharomyces cerevisiae has already been used for heterologous production of fuel chemicals and valuable natural products. The establishment of complicated heterologous biosynthetic pathways in S. cerevisiae became the research focus of Synthetic Biology and Metabolic Engineering. Thus, simple and efficient genomic integration techniques of large number of transcription units are demanded urgently.ResultsAn efficient DNA assembly and chromosomal integration method was created by combining homologous recombination (HR) in S. cerevisiae and Golden Gate DNA assembly method, designated as modularized two-step (M2S) technique. Two major assembly steps are performed consecutively to integrate multiple transcription units simultaneously. In Step 1, Modularized scaffold containing a head-to-head promoter module and a pair of terminators was assembled with two genes. Thus, two transcription units were assembled with Golden Gate method into one scaffold in one reaction. In Step 2, the two transcription units were mixed with modules of selective markers and integration sites and transformed into S. cerevisiae for assembly and integration. In both steps, universal primers were designed for identification of correct clones. Establishment of a functional β-carotene biosynthetic pathway in S. cerevisiae within 5 days demonstrated high efficiency of this method, and a 10-transcriptional-unit pathway integration illustrated the capacity of this method.ConclusionsModular design of transcription units and integration elements simplified assembly and integration procedure, and eliminated frequent designing and synthesis of DNA fragments in previous methods. Also, by assembling most parts in Step 1 in vitro, the number of DNA cassettes for homologous integration in Step 2 was significantly reduced. Thus, high assembly efficiency, high integration capacity, and low error rate were achieved.Electronic supplementary materialThe online version of this article (doi:10.1186/s13068-016-0645-4) contains supplementary material, which is available to authorized users.

Highlights

  • Saccharomyces cerevisiae has already been used for heterologous production of fuel chemicals and valuable natural products

  • Design and construction of modular parts for dual‐transcription unit assembly (Step 1) A functional transcription unit in S. cerevisiae includes at least a promoter (Pro), a gene coding sequence (Gene), and a terminator (Ter)

  • Two terminators were inserted into scaffold plasmid of Step 1 assembly, with dedicated homologous sequences (L1 and L2) lying on both sides of them, which were designed for assembly with modules in Step 2

Read more

Summary

Introduction

Saccharomyces cerevisiae has already been used for heterologous production of fuel chemicals and valuable natural products. Saccharomyces cerevisiae is a prominent model organism in the field of Synthetic Biology and Metabolic Engineering It has already been used for heterologous production of fuel chemicals and valuable natural compounds, such as artemisinin [1, 2], taxol [3], ginsenosides [4], and. One of the most mature methods was developed by Huimin Zhao’s group [10, 11], whose DNA assembler method is able to assemble multiple DNA cassettes in S. cerevisiae, either on a plasmid or on a chromosome To demonstrate their technique, zeaxanthin and aureothin biosynthetic pathways were successfully constructed and proved to be functional [10, 12, 13].

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call