Genomic integration of genes and pathway-sized DNA cassettes is often an indispensable way to construct robust and productive microbial cell factories. For some uncommon microbial hosts, such as Mycolicibacterium and Mycobacterium species, however, it is a challenge. Here, we present a multiplexed integrase-assisted site-specific recombination (miSSR) method to precisely and iteratively integrate genes/pathways with controllable copies in the chromosomes of Mycolicibacteria for the purpose of developing cell factories. First, a single-step multi-copy integration method was established in M. neoaurum by a combination application of mycobacteriophage L5 integrase and two-step allelic exchange strategy, the efficiencies of which were ∼100% for no more than three-copy integration events and decreased sharply to ∼20% for five-copy integration events. Second, the R4, Bxb1 and ΦC31 bacteriophage Att/Int systems were selected to extend the available integration toolbox for multiplexed gene integration events. Third, a reconstructed mycolicibacterial Xer recombinases (Xer-cise) system was employed to recycle the selection marker of gene recombination to facilitate the iterative gene manipulation. As a proof of concept, the biosynthetic pathway of ergothioneine (EGT) in Mycolicibacterium neoaurum ATCC 25795 was achieved by remodeling its metabolic pathway with a miSSR system. With six copies of the biosynthetic gene clusters (BGCs) of EGT and pentose phosphate isomerase (PRT), the titer of EGT in the resulting strain in a 30 mL shake flask within 5 days was enhanced to 66 mg/L, which was 3.77 times of that in the wild strain. The improvements indicated that the miSSR system was an effective, flexible, and convenient tool to engineer the genomes of Mycolicibacteria as well as other strains in the Mycobacteriaceae due to their proximate evolutionary relationships.
Keywords: AE, allelic exchange; Att/Int, attachment/integration; BGCs, biosynthetic gene clusters; CRISPR, clustered regularly interspaced short palindromic repeats; DSBs, double-strand breaks; EGFP, enhanced green fluorescent proteins; EGT, ergothioneine; HPLC, high-performance liquid chromatography; HR, homologous recombination; MSGE, multiplexed site-specific genome engineering; Multi-copy integration; Mycolicibacterium; NHEJ, nonhomologous end-joining; PAM, protospacer adjacent motif; Phage integrase; Site-specific recombination; TB, tuberculosis; Xer recombinases; Xer-cise, Xer recombinases; aMSGE, advanced multiplex site-specific genome engineering; attB, bacterial attachment site; attP, phage attachment site; miSSR, multiplexed integrase-assisted site-specific recombination.
© 2022 The Authors.