Murtas Giovanni
Research Centre Enrico Fermi, Compendio del Viminale, 00184 Rome, Italy.
Orig Life Evol Biosph. 2007 Oct;37(4-5):419-22. doi: 10.1007/s11084-007-9090-5. Epub 2007 Aug 1.
Using a Synthetic Biology approach we are building a semi-synthetic minimal cell. This represents an exercise to shape a minimal-cell model system recalling the simplicity of early living cells in early evolution. We have recently introduced into liposome compartments a minimal set of enzymes named "Puresystem" (PS) synthesizing EGFP proteins. To establish reproduction of the shell compartment with a minimal set of genes we have cloned the genes for the Fatty Acid Synthase (FAS) type I enzymes. These FAS genes introduced into liposomes, translated into FAS enzymes by PS and in the presence of precursors produce fatty acids. The resulting release of fatty acid molecules within liposome vesicles should promote vesicle growth and reproduction. The core reproduction of a minimal cell corresponding to the replication of the minimal genome will require a few genes for the DNA replication and the PS, and a minimum set of genes for the synthesis of t-RNAs. In future the reconstruction of a minimal ribosome will bring the number of genes for ribosomal proteins from 54 of an existing minimal genome down to 30-20 genes. A Synthetic Biology approach could bring the number of essential genes for a minimal cell down to 100 or less.
我们正在运用合成生物学方法构建一个半合成的最小细胞。这是一项塑造最小细胞模型系统的尝试,让人回想起早期进化中原始活细胞的简单性。我们最近已将一组名为“纯净系统”(PS)的最小化酶引入脂质体隔室,该系统可合成绿色荧光蛋白(EGFP)。为了用一组最小化的基因实现外壳隔室的复制,我们克隆了I型脂肪酸合酶(FAS)的基因。这些引入脂质体的FAS基因由PS翻译为FAS酶,并在前体存在的情况下产生脂肪酸。脂质体囊泡内脂肪酸分子的释放应会促进囊泡的生长和复制。与最小基因组复制相对应的最小细胞的核心复制将需要一些用于DNA复制的基因和PS,以及一组用于合成tRNA的最小化基因。未来,最小核糖体的重建将使核糖体蛋白的基因数量从现有最小基因组的54个减少到20至30个基因。合成生物学方法可能会使最小细胞的必需基因数量减少到100个或更少。