Selection-free whole genome transplantation revives dead microbes

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Authors: Zumra Peksaglam Seidel, Nacyra Assad-Garcia, Vanya Paralanov, Feilun Wu, Olivia Chao, Elizabeth A. Strychalski, Eugenia F. Romantseva, Tyler Goshia, J. Craig Venter, John I. Glass
Cited by: 2
References: 30

Abstract

ABSTRACT We present a living, synthetic bacterial cell made by transplanting a complete genome into a dead cell. After killing Mycoplasma capricolum cells by chemically crosslinking their genome with Mitomycin C (MMC), we installed synthetic Mycoplasma mycoides genomes into the resulting dead cells using Whole Genome Transplantation (WGT) 1,2 . During WGT, a synthetic donor genome is placed into a recipient cell, thereby reprogramming that cell to adopt a new genetic identity 3 . WGT has only been demonstrated using species within one phylogenetic clade of Mollicutes bacteria 4 . A major barrier to expanding WGT to diverse bacterial species has been the inability to inactivate the recipient genome, leading to false positive transplants due to homologous recombination of antibiotic resistance markers from the donor genome into the recipient cell genome. Here, we address this key limitation by removing reliance on an antibiotic resistance marker to select for transplants; recipient cells are dead unless revived by the installation of a new genome. Our work demonstrates a general approach to fully inactivate the recipient cell genome, reports the first living synthetic bacterial cell constructed from non-living parts, and advances WGT for building engineered or synthetic cells for diverse applications.

Fields of Study & Subjects

Bacterial Genetics and Biotechnology Microbial infections and disease research CRISPR and Genetic Engineering

Publication details

Journal / source
bioRxiv (Cold Spring Harbor Laboratory)
Publisher
openRxiv
Publication date
14 March 2026
Language
EN
Document type
Preprint