Protein synthesis in liposomes with a minimal set of enzymes.

In a significant step towards the construction of the semi-synthetic minimal cell, a protein expression system with a minimal set of pure and specific enzymes is required. A novel cell-free transcription and translation system named PURESYSTEM (PS), consisting of a specified set of 36 enzymes and ribosomes, has been entrapped in POPC liposomes for protein synthesis. The PS has been used to transcribe and translate an Enhanced Green Fluorescent Protein (EGFP) gene from plasmid DNA. The synthesis is confirmed by the EGFP fluorescence emitting liposomes on fluorometric analysis and on confocal microscopy analysis. Furthermore the PS encapsulated into POPC liposomes can drive the expression of the plsB and plsC genes encoding for the sn-glycerol-3-phosphate acyltransferase (GPAT) and 1-acyl-sn-glycerol-3-phosphate acyltransferase (LPAAT) involved in the first step of the "salvage pathway" for synthesis of POPC. The expression of GPAT and LPAAT in liposomes would in principle allow the production of the cell boundary from within.

[1]  P. Luisi,et al.  Toward the engineering of minimal living cells , 2002, The Anatomical record.

[2]  J. Coleman Characterization of the Escherichia coli gene for 1-acyl-sn-glycerol-3-phosphate acyltransferase (pIsC) , 1992, Molecular and General Genetics MGG.

[3]  A. Pohorille,et al.  Artificial cells: prospects for biotechnology. , 2002, Trends in biotechnology.

[4]  F. Young Biochemistry , 1955, The Indian Medical Gazette.

[5]  M Wakabayashi,et al.  Synthesis of functional protein in liposome. , 2001, Journal of bioscience and bioengineering.

[6]  Fabio Mavelli,et al.  A Possible Route to Prebiotic Vesicle Reproduction , 2004, Artificial Life.

[7]  Vincent Noireaux,et al.  A vesicle bioreactor as a step toward an artificial cell assembly. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[8]  Pier Luigi Luisi,et al.  Liposome-mediated enzymatic synthesis of phosphatidylcholine as an approach to self-replicating liposomes , 1991 .

[9]  P. Luisi,et al.  The Use of Liposomes for Constructing Cell Models , 2002, Journal of biological physics.

[10]  Pier Luigi Luisi,et al.  The Notion of a DNA Minimal Cell: A General Discourse and Some Guidelines for an Experimental Approach , 2002 .

[11]  P. Luisi,et al.  Enzymatic RNA replication in self-reproducing vesicles: an approach to a minimal cell. , 1995, Biochemical and biophysical research communications.

[12]  Tetsuya Yomo,et al.  Expression of a cascading genetic network within liposomes , 2004, FEBS letters.

[13]  P. Luisi,et al.  Polymerase chain reaction in liposomes. , 1995, Chemistry & biology.

[14]  C. Hutchison,et al.  Essential genes of a minimal bacterium. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[15]  P. Luisi,et al.  Autopoietic Self-Reproduction of Fatty Acid Vesicles , 1994 .

[16]  E V Koonin,et al.  How many genes can make a cell: the minimal-gene-set concept. , 2000, Annual review of genomics and human genetics.

[17]  H. Morowitz Beginnings of Cellular Life: Metabolism Recapitulates Biogenesis , 1992 .

[18]  W. Wilkison,et al.  sn-Glycerol-3-phosphate acyltransferase from Escherichia coli. , 1997, Biochimica et biophysica acta.

[19]  Pier Luigi Luisi,et al.  A Chemical Model of Homeostasis. , 2001, Angewandte Chemie.

[20]  Takuya Ueda,et al.  Cell-free translation reconstituted with purified components , 2001, Nature Biotechnology.

[21]  A. Moya,et al.  Determination of the Core of a Minimal Bacterial Gene Set , 2004, Microbiology and Molecular Biology Reviews.

[22]  C. Yanisch-Perron,et al.  Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors. , 1985, Gene.