生物
基因组
软体动物
类支原体
支原体
移植
遗传学
微生物学
细菌基因组大小
细菌
全基因组测序
水平基因转移
抗生素耐药性
合成生物学
重编程
细胞
基因
丝裂霉素C
流动遗传元素
铜绿假单胞菌
计算生物学
病毒学
去肽
支原体科
基因组工程
抗生素
作者
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
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2026-03-14
被引量:1
标识
DOI:10.64898/2026.03.13.711674
摘要
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.
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