In vivo evidence for the involvement of anionic phospholipids in initiation of DNA replication in Escherichia coli.
about
A retrospective: use of Escherichia coli as a vehicle to study phospholipid synthesis and functionThe PEL1 gene (renamed PGS1) encodes the phosphatidylglycero-phosphate synthase of Saccharomyces cerevisiae.Random versus Cell Cycle-Regulated Replication Initiation in Bacteria: Insights from Studying Vibrio cholerae Chromosome 2Mutations in DnaA protein suppress the growth arrest of acidic phospholipid-deficient Escherichia coli cells.Multiple regulatory systems coordinate DNA replication with cell growth in Bacillus subtilisEscherichia coli DnaA forms helical structures along the longitudinal cell axis distinct from MreB filaments.A gene encoding phosphatidylethanolamine N-methyltransferase from Acetobacter aceti and some properties of its disruptant.Amphitropic proteins: regulation by reversible membrane interactions (review).DnaA, the initiator of Escherichia coli chromosomal replication, is located at the cell membraneCalorimetric and spectroscopic studies of the thermotropic phase behavior of the n-saturated 1,2-diacylphosphatidylglycerols.Transmembrane protein topology mapping by the substituted cysteine accessibility method (SCAM(TM)): application to lipid-specific membrane protein topogenesisDiversity and versatility of lipid-protein interactions revealed by molecular genetic approaches.A SeqA hyperstructure and its interactions direct the replication and sequestration of DNA.Tuning the membrane surface potential for efficient toxin import.Dispensable nature of phosphatidylglycerol in Escherichia coli: dual roles of anionic phospholipids.Association of the chromosome replication initiator DnaA with the Escherichia coli inner membrane in vivo: quantity and mode of binding.Crosstalk between DnaA protein, the initiator of Escherichia coli chromosomal replication, and acidic phospholipids present in bacterial membranes.E. coli MG1655 modulates its phospholipid composition through the cell cycle.Specific genomic sequences of E. coli promote replicational initiation by directly reactivating ADP-DnaA.Phosphatidylinositol cannot substitute for phosphatidylglycerol in supporting cell growth of Escherichia coli.Isolation and expression of the Rhodobacter sphaeroides gene (pgsA) encoding phosphatidylglycerophosphate synthaseMembrane regulation of the chromosomal replication activity of E.coli DnaA requires a discrete site on the protein.Membrane regulation of the chromosomal replication activity of E. coli DnaA requires a discrete site on the protein.Nucleotide-Induced Conformational Changes in Escherichia coli DnaA Protein Are Required for Bacterial ORC to Pre-RC Conversion at the Chromosomal Origin.Regulatory network of the initiation of chromosomal replication in Escherichia coli.Stable DNA replication: interplay between DNA replication, homologous recombination, and transcriptionAlteration in the contents of unsaturated fatty acids in dnaA mutants of Escherichia coli.Pleiotropic roles of polyglycerolphosphate synthase of lipoteichoic acid in growth of Staphylococcus aureus cells.Reduced lipopolysaccharide phosphorylation in Escherichia coli lowers the elevated ori/ter ratio in seqA mutantsRequirement of phosphatidylglycerol for photosynthetic function in thylakoid membranes.Molecular genetic approaches to defining lipid function.Activation of the Rcs signal transduction system is responsible for the thermosensitive growth defect of an Escherichia coli mutant lacking phosphatidylglycerol and cardiolipin.Regulating DNA replication in bacteria.Is phosphatidylglycerol essential for terrestrial life?Viability of an Escherichia coli pgsA null mutant lacking detectable phosphatidylglycerol and cardiolipin.Visualization of phospholipid domains in Escherichia coli by using the cardiolipin-specific fluorescent dye 10-N-nonyl acridine orange.Envelope disorder of Escherichia coli cells lacking phosphatidylglycerolWhy do bacteria divide?Suppression of initiation defects of chromosome replication in Bacillus subtilis dnaA and oriC-deleted mutants by integration of a plasmid replicon into the chromosomes.Rhizobium meliloti mutants deficient in phospholipid N-methyltransferase still contain phosphatidylcholine.
P2860
Q26995227-6F5E3BEF-2B50-4B91-AF3A-963F05BA4BF3Q27931115-5B5E0851-4453-4F6B-A9EC-A256A3D204BAQ28077720-9C48E824-5F2E-477D-8EB3-E3967C79CA2DQ28354843-5E5D9DC5-9632-4D78-A164-C62D1E2173E7Q28544015-709F6A41-30D2-4423-8F8C-B4E977863124Q30494952-D99900A8-5376-4ABA-B478-C98F911AD31BQ30806998-6FCC7B45-554D-4D08-8BD7-441A8FD81F41Q33741843-BAD8A44F-2441-45C9-B1DF-D7A0934F303FQ33790421-07987DF2-458E-494F-8C16-63642746BD8DQ33916851-97D30E42-75A9-4F43-BC06-F8B0AE653518Q33922207-FB507B90-BEF7-419D-BA7B-19101E81AFE4Q33944665-84735A37-FC93-4467-9F1F-7180B551B38FQ34023161-2CE37A10-C266-47DE-A706-DF92ACB37F5AQ34065539-F72C9203-EC12-4BCB-8FEA-61E4E90E93FFQ34190660-8E448ACD-3CE4-4665-A1AC-ED5123DA4D91Q34264677-15ACE64F-5590-4FC0-BC83-53E4A62F8BECQ34339951-27DE60F8-5F86-4EB2-AEB6-504EB0448D67Q34489533-57957D2E-A9C4-4249-A03D-E7AE0059E9CFQ34978255-4F03A3FA-8C60-4C9C-9626-F359109859E4Q35586284-BA2B26C8-5BCD-4766-ACC6-E2B2FB3923B3Q35602525-78E92978-BB94-4BFF-93E6-3AF34F7C62DFQ35849725-0542AA75-BB75-43B3-A581-C98075AE1C9CQ35900550-75F94E76-8F9C-4ED4-A302-392244625FCCQ36324820-9B4C0D0D-2FAC-4458-8CFA-22D430855BF2Q36336528-6BB19602-6650-42D5-9F80-8AE5C0A49EA8Q36574251-09E3E083-B15F-4D06-A05B-5F464C818E41Q36896747-23ADE5C4-09C1-42D3-BBFB-B997925B2AA5Q37033429-13B04D4D-9FC4-4740-8634-812A2D291839Q37214505-602EDD11-2E5B-400D-92C6-736E2CB2C2BEQ37255359-CB924E51-09E7-4C34-A82C-53B0EAA7B345Q37316193-C5CB8D84-1947-4332-AC3B-F106BF3E0E43Q37513693-F22F3352-A258-4F89-948D-861018BA8E60Q38087526-C988D994-18A9-4FFC-BCF2-04482D00687BQ39013532-E368BD9A-7F46-4BC0-92F4-0124BD59AE1CQ39498543-9812E67B-947A-4F71-B834-AD9FE4A08358Q39499180-7FD2427E-DF2F-41F5-9BE0-14D8AFFD7BE1Q39680498-17554CEC-1402-4C6D-AE65-A8A63F74CECDQ39691590-C225E9D7-8A75-4EF1-A6F3-13538753A7DBQ39845285-361B5364-E915-4341-8904-7BBF6F086F9EQ39847851-51EF41BD-F7FD-4233-A782-41336EEE90B1
P2860
In vivo evidence for the involvement of anionic phospholipids in initiation of DNA replication in Escherichia coli.
description
1995 nî lūn-bûn
@nan
1995 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
In vivo evidence for the invol ...... plication in Escherichia coli.
@ast
In vivo evidence for the invol ...... plication in Escherichia coli.
@en
In vivo evidence for the invol ...... plication in Escherichia coli.
@nl
type
label
In vivo evidence for the invol ...... plication in Escherichia coli.
@ast
In vivo evidence for the invol ...... plication in Escherichia coli.
@en
In vivo evidence for the invol ...... plication in Escherichia coli.
@nl
prefLabel
In vivo evidence for the invol ...... plication in Escherichia coli.
@ast
In vivo evidence for the invol ...... plication in Escherichia coli.
@en
In vivo evidence for the invol ...... plication in Escherichia coli.
@nl
P2860
P356
P1476
In vivo evidence for the invol ...... plication in Escherichia coli.
@en
P2860
P304
P356
10.1073/PNAS.92.3.783
P407
P577
1995-01-01T00:00:00Z