Bacterial chromosome segregation
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[1] E. Harry,et al. Bacterial cell division: regulating Z‐ring formation , 2001, Molecular microbiology.
[2] G. Węgrzyn,et al. Inheritance of the replication complex: a unique or common phenomenon in the control of DNA replication? , 2001, Archives of Microbiology.
[3] P. Graumann. Bacillus subtilis SMC Is Required for Proper Arrangement of the Chromosome and for Efficient Segregation of Replication Termini but Not for Bipolar Movement of Newly Duplicated Origin Regions , 2000, Journal of bacteriology.
[4] A. Grossman,et al. Bipolar localization of a chromosome partition protein in Bacillus subtilis. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[5] D. Biek,et al. A single 43-bp sopC repeat of plasmid mini-F is sufficient to allow assembly of a functional nucleoprotein partition complex. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[6] J. Gober,et al. The chromosome partitioning protein, ParB, is required for cytokinesis in Caulobacter crescentus , 2001, Molecular microbiology.
[7] T. Ogura,et al. Structure and function of the F plasmid genes essential for partitioning. , 1986, Journal of molecular biology.
[8] Tania A Baker,et al. Polymerases and the Replisome: Machines within Machines , 1998, Cell.
[9] H. Erickson,et al. Straight and Curved Conformations of FtsZ Are Regulated by GTP Hydrolysis , 2000, Journal of bacteriology.
[10] B. Funnell. Participation of Escherichia coli integration host factor in the P1 plasmid partition system. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[11] R. B. Jensen,et al. The Caulobacter crescentus smc gene is required for cell cycle progression and chromosome segregation. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[12] G. Węgrzyn,et al. Composition of the lambda plasmid heritable replication complex. , 2002, The Biochemical journal.
[13] J. Löwe,et al. Distribution of the Escherichia coli structural maintenance of chromosomes (SMC)‐like protein MukB in the cell , 2001, Molecular microbiology.
[14] W. Margolin,et al. Localization of Cell Division Protein FtsK to theEscherichia coli Septum and Identification of a Potential N-Terminal Targeting Domain , 1998, Journal of bacteriology.
[15] Moselio Schaechter,et al. The replicative origin of the E. coli chromosome binds to cell membranes only when hemimethylated , 1988, Cell.
[16] D. Lane,et al. The parAB gene products of Pseudomonas putida exhibit partition activity in both P. putida and Escherichia coli , 2002, Molecular microbiology.
[17] K. Skarstad,et al. SeqA, the Escherichia coli origin sequestration protein, is also a specific transcription factor , 2001, Molecular microbiology.
[18] O. Espéli,et al. A Physical and Functional Interaction between Escherichia coli FtsK and Topoisomerase IV* , 2003, Journal of Biological Chemistry.
[19] L. Gagnier,et al. The P1 plasmid partition complex at parS. II. Analysis of ParB protein binding activity and specificity. , 1993, The Journal of biological chemistry.
[20] J. Gober,et al. ParB-stimulated nucleotide exchange regulates a switch in functionally distinct ParA activities. , 2002, Molecular cell.
[21] S. Austin,et al. The P1 plasmid-partition system synthesizes two essential proteins from an autoregulated operon. , 1988, Plasmid.
[22] I. Borovok,et al. Gene organization in the trxA/B-oriC region of the Streptomyces coelicolor chromosome and comparison with other eubacteria. , 1998, Gene.
[23] J. Hoch,et al. Control of the initiation of sporulation in Bacillus subtilis by a phosphorelay. , 1991, Research in microbiology.
[24] J. Gober,et al. Cell Cycle–Dependent Polar Localization of Chromosome Partitioning Proteins in Caulobacter crescentus , 1997, Cell.
[25] S. Austin,et al. Segregation of the Escherichia coli chromosome terminus , 2003, Molecular microbiology.
[26] A. Grossman,et al. The extrusion-capture model for chromosome partitioning in bacteria. , 2001, Genes & development.
[27] H. Seitz,et al. Strand‐specific loading of DnaB helicase by DnaA to a substrate mimicking unwound oriC , 2002, Molecular microbiology.
[28] J. Surtees,et al. Stoichiometry of P1 Plasmid Partition Complexes* , 2000, The Journal of Biological Chemistry.
[29] K. Skarstad,et al. Escherichia coli SeqA protein affects DNA topology and inhibits open complex formation at oriC , 1999, The EMBO journal.
[30] S. Moriya,et al. Increasing the Ratio of Soj to Spo0J Promotes Replication Initiation in Bacillus subtilis , 2003, Journal of bacteriology.
[31] E. Bi,et al. FtsZ ring structure associated with division in Escherichia coli , 1991, Nature.
[32] A. Murray,et al. Chromosome and Low Copy Plasmid Segregation in E. coli: Visual Evidence for Distinct Mechanisms , 1997, Cell.
[33] P. Yates,et al. The F plasmid centromere, sopC, is required for full repression of the sopAB operon. , 1999, Journal of molecular biology.
[34] J. Sawitzke,et al. A case for sliding SeqA tracts at anchored replication forks during Escherichia coli chromosome replication and segregation , 2000, The EMBO journal.
[35] H. Yoshikawa,et al. Genes and their organization in the replication origin region of the bacterial chromosome , 1992, Molecular microbiology.
[36] S. Tamaki,et al. Mutant isolation and molecular cloning of mre genes, which determine cell shape, sensitivity to mecillinam, and amount of penicillin-binding proteins in Escherichia coli , 1987, Journal of bacteriology.
[37] S. Hiraga,et al. Sister chromosome cohesion of Escherichia coli , 2001, Molecular microbiology.
[38] S. Austin,et al. The P1 plasmid in action: time-lapse photomicroscopy reveals some unexpected aspects of plasmid partition. , 2002, Plasmid.
[39] C. Dingman. Bidirectional chromosome replication: some topological considerations. , 1974, Journal of theoretical biology.
[40] J. Soppa,et al. Cell cycle‐dependent expression of an essential SMC‐like protein and dynamic chromosome localization in the archaeon Halobacterium salinarum , 2002, Molecular microbiology.
[41] J. Errington,et al. Polar localization of the MinD protein of Bacillus subtilis and its role in selection of the mid-cell division site. , 1998, Genes & development.
[42] A. Leonard,et al. Building a bacterial orisome: emergence of new regulatory features for replication origin unwinding , 2004, Molecular microbiology.
[43] W. Donachie,et al. The cytoplasmic domain of FtsK protein is required for resolution of chromosome dimers , 1999, Molecular microbiology.
[44] K. Chater,et al. The ParB protein of Streptomyces coelicolor A3(2) recognizes a cluster of parS sequences within the origin‐proximal region of the linear chromosome , 2002, Molecular microbiology.
[45] M. Davis,et al. Recognition of the P1 plasmid centromere analog involves binding of the ParB protein and is modified by a specific host factor. , 1988, The EMBO journal.
[46] Peter Roepstorff,et al. Bacterial mitosis: ParM of plasmid R1 moves plasmid DNA by an actin-like insertional polymerization mechanism. , 2003, Molecular cell.
[47] S. Austin,et al. The P1 plasmid is segregated to daughter cells by a ‘capture and ejection’ mechanism coordinated with Escherichia coli cell division , 2002, Molecular microbiology.
[48] Christopher M Thomas,et al. Effect of growth rate and incC mutation on symmetric plasmid distribution by the IncP‐1 partitioning apparatus , 1999, Molecular microbiology.
[49] W. Messer. The bacterial replication initiator DnaA. DnaA and oriC, the bacterial mode to initiate DNA replication. , 2002, FEMS microbiology reviews.
[50] N. Ravin,et al. Mapping of functional domains in F plasmid partition proteins reveals a bipartite SopB-recognition domain in SopA. , 2003, Journal of molecular biology.
[51] P. Silver,et al. Use of time‐lapse microscopy to visualize rapid movement of the replication origin region of the chromosome during the cell cycle in Bacillus subtilis , 1998, Molecular microbiology.
[52] B. Funnell,et al. Intracellular localization of P1 ParB protein depends on ParA and parS. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[53] J. Gober,et al. Productive interaction between the chromosome partitioning proteins, ParA and ParB, is required for the progression of the cell cycle in Caulobacter crescentus , 2003, Molecular microbiology.
[54] P. Graumann,et al. Actin-like Proteins MreB and Mbl from Bacillus subtilis Are Required for Bipolar Positioning of Replication Origins , 2003, Current Biology.
[55] A. Grossman,et al. Movement of replicating DNA through a stationary replisome. , 2000, Molecular cell.
[56] Y. Kasahara,et al. Two separate DNA sequences within oriC participate in accurate chromosome segregation in Bacillus subtilis , 2002, Molecular microbiology.
[57] J. Beckwith,et al. Assembly of cell division proteins at the E. coli cell center. , 2002, Current opinion in microbiology.
[58] R. B. Jensen,et al. Partitioning of plasmid R1. The ParM protein exhibits ATPase activity and interacts with the centromere-like ParR-parC complex. , 1997, Journal of molecular biology.
[59] D. Sherratt,et al. FtsK Is a DNA Motor Protein that Activates Chromosome Dimer Resolution by Switching the Catalytic State of the XerC and XerD Recombinases , 2002, Cell.
[60] Christopher M Thomas,et al. IncC of Broad-Host-Range Plasmid RK2 Modulates KorB Transcriptional Repressor Activity In Vivo and Operator Binding In Vitro , 1999, Journal of bacteriology.
[61] A. Grossman,et al. Cell cycle and sporulation in Bacillus subtilis. , 1998, Current opinion in microbiology.
[62] K. Chater,et al. Partitioning of the Linear Chromosome during Sporulation of Streptomyces coelicolor A3(2) Involves an oriC-Linked parAB Locus , 2000, Journal of bacteriology.
[63] A. Grossman,et al. Localization of bacterial DNA polymerase: evidence for a factory model of replication. , 1998, Science.
[64] H. Niki,et al. Bidirectional migration of SeqA‐bound hemimethylated DNA clusters and pairing of oriC copies in Escherichia coli , 2000, Genes to cells : devoted to molecular & cellular mechanisms.
[65] K. Pogliano,et al. The Membrane Domain of SpoIIIE Is Required for Membrane Fusion during Bacillus subtilis Sporulation , 2003, Journal of bacteriology.
[66] T. Ogura,et al. E.coli MukB protein involved in chromosome partition forms a homodimer with a rod‐and‐hinge structure having DNA binding and ATP/GTP binding activities. , 1992, The EMBO journal.
[67] T. Kruse,et al. Dysfunctional MreB inhibits chromosome segregation in Escherichia coli , 2003, The EMBO journal.
[68] R. Lewis,et al. Chromosome loss from par mutants of Pseudomonas putida depends on growth medium and phase of growth. , 2002, Microbiology.
[69] J. Reeve,et al. Minicells of Bacillus subtilis , 1973, Journal of bacteriology.
[70] W. Margolin,et al. Themes and variations in prokaryotic cell division. , 2000, FEMS microbiology reviews.
[71] A. Węgrzyn,et al. SeqA‐mediated stimulation of a promoter activity by facilitating functions of a transcription activator , 2003, Molecular microbiology.
[72] Tohru Mizushima,et al. Acidic phospholipids inhibit the DNA‐binding activity of DnaA protein, the initiator of chromosomal DNA replication in Escherichia coli , 2002, Molecular microbiology.
[73] A. Grossman,et al. Identification and Characterization of a Bacterial Chromosome Partitioning Site , 1998, Cell.
[74] Christopher M Thomas,et al. Functional dissection of the ParB homologue (KorB) from IncP-1 plasmid RK2. , 2002, Nucleic acids research.
[75] H. Niki,et al. Active segregation by the Bacillus subtilis partitioning system in Escherichia coli. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[76] Y. Brun,et al. Cell cycle and positional constraints on FtsZ localization and the initiation of cell division in Caulobacter crescentus , 2001, Molecular microbiology.
[77] A. Grossman,et al. spo0J is required for normal chromosome segregation as well as the initiation of sporulation in Bacillus subtilis , 1994, Journal of bacteriology.
[78] J. Errington,et al. Bacillus subtilis SpoIIIE protein required for DNA segregation during asymmetric cell division. , 1994, Science.
[79] D. Sherratt,et al. Escherichia coli XerC recombinase is required for chromosomal segregation at cell division. , 1991, The New biologist.
[80] J. Errington,et al. Characterization of the parB-Like yyaA Gene of Bacillus subtilis , 2002, Journal of bacteriology.
[81] J. Bouet,et al. P1 ParA interacts with the P1 partition complex at parS and an ATP–ADP switch controls ParA activities , 1999, The EMBO journal.
[82] J. Sawitzke,et al. An analysis of the factory model for chromosome replication and segregation in bacteria , 2001, Molecular microbiology.
[83] D. Koshland,et al. SMC1: an essential yeast gene encoding a putative head-rod-tail protein is required for nuclear division and defines a new ubiquitous protein family , 1993, The Journal of cell biology.
[84] J. Gober,et al. Regulation of cellular differentiation in Caulobacter crescentus , 1995, Microbiological reviews.
[85] T. Hirano. Chromosome cohesion, condensation, and separation. , 2000, Annual review of biochemistry.
[86] J. Swedlow,et al. The SMC family: from chromosome condensation to dosage compensation. , 1995, Current opinion in cell biology.
[87] R. Jessberger,et al. Structural maintenance of chromosomes (SMC) proteins: conserved molecular properties for multiple biological functions. , 1999, European journal of biochemistry.
[88] H. Kowarzyk. Structure and Function. , 1910, Nature.
[89] A. Grossman,et al. Control of Sporulation Gene Expression in Bacillus subtilis by the Chromosome Partitioning Proteins Soj (ParA) and Spo0J (ParB) , 2000, Journal of bacteriology.
[90] D. Bastia,et al. Termination of DNA replication in vitro: requirement for stereospecific interaction between two dimers of the replication terminator protein of Bacillus subtilis and with the terminator site to elicit polar contrahelicase and fork impedance. , 1995, The EMBO journal.
[91] Yu-Ling Shih,et al. Division site selection in Escherichia coli involves dynamic redistribution of Min proteins within coiled structures that extend between the two cell poles , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[92] SISTER CHROMATID EXCHANGE FREQUENCIES IN LYMPHOCYTES , 1984, The Lancet.
[93] F. Neidhardt,et al. Escherichia Coli and Salmonella: Typhimurium Cellular and Molecular Biology , 1987 .
[94] Stuart Austin,et al. The segregation of the Escherichia coli origin and terminus of replication , 2002, Molecular microbiology.
[95] W. Donachie,et al. Coupling the initiation of chromosome replication to cell size in Escherichia coli. , 2003, Current opinion in microbiology.
[96] A. Grossman,et al. Interactions among mutations that cause altered timing of gene expression during sporulation in Bacillus subtilis , 1992, Journal of bacteriology.
[97] Z. Kelman,et al. DNA polymerase III holoenzyme: structure and function of a chromosomal replicating machine. , 1995, Annual review of biochemistry.
[98] Jan Löwe,et al. F‐actin‐like filaments formed by plasmid segregation protein ParM , 2002, The EMBO journal.
[99] W. D. Fisher,et al. MINIATURE escherichia coli CELLS DEFICIENT IN DNA. , 1967, Proceedings of the National Academy of Sciences of the United States of America.
[100] K. Skarstad,et al. The Escherichia coli SeqA protein binds specifically and co‐operatively to two sites in hemimethylated and fully methylated oriC , 2000, Molecular microbiology.
[101] H. Mori,et al. Partitioning of the F plasmid: Overproduction of an essential protein for partition inhibits plasmid maintenance , 1987, Molecular and General Genetics MGG.
[102] H. Niki,et al. Subcellular Distribution of Actively Partitioning F Plasmid during the Cell Division Cycle in E. coli , 1997, Cell.
[103] A. Grossman,et al. Characterization of a prokaryotic SMC protein involved in chromosome partitioning. , 1998, Genes & development.
[104] R. B. Jensen,et al. Plasmid and chromosome partitioning: surprises from phylogeny , 2000, Molecular microbiology.
[105] Kojima. Structure and function , 2005 .
[106] D. Lane,et al. Disruption of the F plasmid partition complex in vivo by partition protein SopA , 2000, Molecular microbiology.
[107] L. Rothfield,et al. A division inhibitor and a topological specificity factor coded for by the minicell locus determine proper placement of the division septum in E. coli , 1989, Cell.
[108] H. Niki,et al. New topoisomerase essential for chromosome segregation in E. coli , 1990, Cell.
[109] B. Funnell,et al. The P1 plasmid partition protein ParA. A role for ATP in site-specific DNA binding. , 1994, The Journal of biological chemistry.
[110] D. Sherratt,et al. Spatial and temporal organization of replicating Escherichia coli chromosomes , 2003, Molecular microbiology.
[111] H. Erickson,et al. The Symmetrical Structure of Structural Maintenance of Chromosomes (SMC) and MukB Proteins: Long, Antiparallel Coiled Coils, Folded at a Flexible Hinge , 1998, The Journal of cell biology.
[112] Christopher M Thomas,et al. A family of ATPases involved in active partitioning of diverse bacterial plasmids , 1990, Molecular microbiology.
[113] T. Katayama,et al. Replication cycle‐coordinated change of the adenine nucleotide‐bound forms of DnaA protein in Escherichia coli , 1999, The EMBO journal.
[114] K. A. Martin,et al. Specificity switching of the P1 plasmid centromere‐like site. , 1990, The EMBO journal.
[115] C. Woldringh,et al. The Escherichia cohi minB mutation resembles gyrB in defective nucleoid segregation and decreased negative supercoiling of plasmids , 1990, Molecular and General Genetics MGG.
[116] T. Katayama,et al. A Nucleotide Switch in the Escherichia coli DnaA Protein Initiates Chromosomal Replication , 2002, The Journal of Biological Chemistry.
[117] D. Oesterhelt,et al. Discovery of two novel families of proteins that are proposed to interact with prokaryotic SMC proteins, and characterization of the Bacillus subtilis family members ScpA and ScpB , 2002, Molecular microbiology.
[118] M. Davis,et al. Biochemical activities of the ParA partition protein of the P1 plasmid , 1992, Molecular microbiology.
[119] J. Errington,et al. The Bacillus subtilis soj‐spo0J locus is required for a centromere‐like function involved in prespore chromosome partitioning , 1996, Molecular microbiology.
[120] Christopher M Thomas,et al. Active partitioning of bacterial plasmids. , 1992, Journal of general microbiology.
[121] P. Graumann. SMC proteins in bacteria: condensation motors for chromosome segregation? , 2001, Biochimie.
[122] A. Kolstø. Time for a fresh look at the bacterial chromosome. , 1999, Trends in microbiology.
[123] O. Espéli,et al. Temporal regulation of topoisomerase IV activity in E. coli. , 2003, Molecular cell.
[124] K. Pogliano,et al. MinCD‐dependent regulation of the polarity of SpoIIIE assembly and DNA transfer , 2002, The EMBO journal.
[125] M. Yarmolinsky,et al. Plasmid partitioning and the spreading of P1 partition protein ParB , 2004, Molecular microbiology.
[126] D. Hilbert,et al. Sporulation of Bacillus subtilis. , 2004, Current opinion in microbiology.
[127] D. Sherratt,et al. FtsK‐dependent and ‐independent pathways of Xer site‐specific recombination , 1999, The EMBO journal.
[128] J. Hoch. Regulation of the phosphorelay and the initiation of sporulation in Bacillus subtilis. , 1993, Annual review of microbiology.
[129] H. Niki,et al. Complex formation of MukB, MukE and MukF proteins involved in chromosome partitioning in Escherichia coli , 1999, The EMBO journal.
[130] J. Errington,et al. The Bacillus subtilis DivIVA protein targets to the division septum and controls the site specificity of cell division , 1997, Molecular microbiology.
[131] K. Morikawa,et al. Structure of a replication-terminator protein complexed with DNA , 1996, Nature.
[132] M. Yarmolinsky,et al. Effects of the P1 Plasmid Centromere on Expression of P1 Partition Genes , 2002, Journal of bacteriology.
[133] A. Grossman,et al. Effects of the Chromosome Partitioning Protein Spo0J (ParB) on oriC Positioning and Replication Initiation in Bacillus subtilis , 2003, Journal of bacteriology.
[134] K. Skarstad,et al. E. coli SeqA protein binds oriC in two different methyl-modulated reactions appropriate to its roles in DNA replication initiation and origin sequestration , 1995, Cell.
[135] Nancy Kleckner,et al. SeqA: A negative modulator of replication initiation in E. coli , 1994, Cell.
[136] M. Yarmolinsky,et al. Silencing of genes flanking the P1 plasmid centromere. , 1999, Science.
[137] W. Donachie. Co‐ordinate regulation of the Escherichia coli cell cycle or The cloud of unknowing , 2001, Molecular microbiology.
[138] A. Leonard,et al. Two discriminatory binding sites in the Escherichia coli replication origin are required for DNA strand opening by initiator DnaA-ATP. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[139] O. Espéli,et al. SetB: an integral membrane protein that affects chromosome segregation in Escherichia coli , 2003, Molecular microbiology.
[140] D. Biek,et al. Partition functions of mini-F affect plasmid DNA topology in Escherichia coli. , 1995, Journal of molecular biology.
[141] J. Errington,et al. Direct evidence for active segregation of oriC regions of the Bacillus subtilis chromosome and co‐localization with the Spo0J partitioning protein , 1997, Molecular microbiology.
[142] J. Errington,et al. Dynamic, mitotic-like behavior of a bacterial protein required for accurate chromosome partitioning. , 1997, Genes & development.
[143] J. Wang,et al. Role of Bacillus subtilis SpoIIIE in DNA transport across the mother cell-prespore division septum. , 2000, Science.
[144] R. B. Jensen,et al. Prokaryotic DNA segregation by an actin‐like filament , 2002, The EMBO journal.
[145] David J Sherratt,et al. Bacterial Chromosome Dynamics , 2003, Science.
[146] T. Ogura,et al. The new gene mukB codes for a 177 kd protein with coiled‐coil domains involved in chromosome partitioning of E. coli. , 1991, The EMBO journal.
[147] P. Kuempel,et al. Sister Chromatid Exchange Frequencies inEscherichia coli Analyzed by Recombination at thedif Resolvase Site , 1998, Journal of bacteriology.
[148] J. Sawitzke,et al. Suppression of chromosome segregation defects of Escherichia coli muk mutants by mutations in topoisomerase I. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[149] F. Khanim,et al. Repression at a distance by the global regulator KorB of promiscuous IncP plasmids , 1999, Molecular microbiology.
[150] J. Errington,et al. Dynamic movement of the ParA-like Soj protein of B. subtilis and its dual role in nucleoid organization and developmental regulation. , 1999, Molecular cell.
[151] J. Errington,et al. RacA and the Soj‐Spo0J system combine to effect polar chromosome segregation in sporulating Bacillus subtilis , 2003, Molecular microbiology.
[152] D. Sherratt,et al. Circles: The replication-recombination-chromosome segregation connection , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[153] J. Lutkenhaus,et al. Dynamic proteins in bacteria. , 2002, Current opinion in microbiology.
[154] Jonathan Bath,et al. DNA transport in bacteria , 2001, Nature Reviews Molecular Cell Biology.
[155] K. Gerdes,et al. Bacterial mitosis: partitioning protein ParA oscillates in spiral‐shaped structures and positions plasmids at mid‐cell , 2004, Molecular microbiology.
[156] D. O’Callaghan,et al. Differences in chromosome number and genome rearrangements in the genus Brucella , 1998, Molecular microbiology.
[157] P Bork,et al. An ATPase domain common to prokaryotic cell cycle proteins, sugar kinases, actin, and hsp70 heat shock proteins. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[158] R. Losick,et al. RacA, a Bacterial Protein That Anchors Chromosomes to the Cell Poles , 2002, Science.
[159] C. Sáez,et al. Recruitment of MinC, an Inhibitor of Z-Ring Formation, to the Membrane in Escherichia coli: Role of MinD and MinE , 2003, Journal of bacteriology.
[160] A. Grossman,et al. A developmental checkpoint couples the initiation of sporulation to DNA replication in Bacillus subtilis. , 1994, The EMBO journal.
[161] 《中华放射肿瘤学杂志》编辑部. Medline , 2001, Current Biology.
[162] K. Asai,et al. A Bacillus subtilis gene‐encoding protein homologous to eukaryotic SMC motor protein is necessary for chromosome partition , 1998, Molecular microbiology.
[163] N. Cozzarelli,et al. Closing the ring: links between SMC proteins and chromosome partitioning, condensation, and supercoiling. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[164] K. Skarstad,et al. Limiting DNA replication to once and only once , 2000, EMBO reports.
[165] J. Wang,et al. SopB protein-mediated silencing of genes linked to the sopC locus of Escherichia coli F plasmid. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[166] T. Ogura,et al. Chromosome partitioning in Escherichia coli: novel mutants producing anucleate cells , 1989, Journal of bacteriology.
[167] Christopher M Thomas,et al. ParB of Pseudomonas aeruginosa: Interactions with Its Partner ParA and Its Target parS and Specific Effects on Bacterial Growth , 2004, Journal of bacteriology.
[168] J. Pogliano,et al. Compatible bacterial plasmids are targeted to independent cellular locations in Escherichia coli , 2002, The EMBO journal.
[169] S Kaplan,et al. Chromosome transfer in Rhodobacter sphaeroides: Hfr formation and genetic evidence for two unique circular chromosomes , 1992, Journal of bacteriology.
[170] H V Westerhoff,et al. Structure and partitioning of bacterial DNA: determined by a balance of compaction and expansion forces? , 1995, FEMS microbiology letters.
[171] R. Wake. Replication fork arrest and termination of chromosome replication in Bacillus subtilis. , 1997, FEMS microbiology letters.
[172] S. Molin,et al. Partitioning of plasmid R1. Structural and functional analysis of the parA locus. , 1986, Journal of molecular biology.
[173] J. Errington,et al. Control of Cell Shape in Bacteria Helical, Actin-like Filaments in Bacillus subtilis , 2001, Cell.