Bacterial physiology: Setting the speed of translation.
- Published in:
- Nature Reviews Microbiology, 2012, v. 10, n. 6, p. 375, doi. 10.1038/nrmicro2796
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- Article
Works about BACILLUS subtilis genetics
Results: 177
1
2
From Cell Differentiation to Cell Collectives: Bacillus subtilis Uses Division of Labor to Migrate.
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- PLoS Biology, 2015, v. 13, n. 4, p. 1, doi. 10.1371/journal.pbio.1002141
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- Article
3
Characterization and mutation analysis of a halotolerant serine protease from a new isolate of <italic>Bacillus subtilis</italic>.
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- Biotechnology Letters, 2018, v. 40, n. 1, p. 189, doi. 10.1007/s10529-017-2459-2
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- Article
4
Rapid evolution of hyaluronan synthase to improve hyaluronan production and molecular mass in Bacillus subtilis.
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- Biotechnology Letters, 2016, v. 38, n. 12, p. 2103, doi. 10.1007/s10529-016-2193-1
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- Article
5
A high-efficiency recombineering system with PCR-based ssDNA in Bacillus subtilis mediated by the native phage recombinase GP35.
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- Applied Microbiology & Biotechnology, 2015, v. 99, n. 12, p. 5151, doi. 10.1007/s00253-015-6485-5
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- Article
6
What renders Bacilli genetically competent? A gaze beyond the model organism.
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- Applied Microbiology & Biotechnology, 2015, v. 99, n. 4, p. 1557, doi. 10.1007/s00253-014-6316-0
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- Article
7
Enhanced production of 2,3-butanediol by engineered Bacillus subtilis.
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- Applied Microbiology & Biotechnology, 2012, v. 94, n. 3, p. 651, doi. 10.1007/s00253-011-3774-5
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- Article
8
Bacterial abl-like genes: production of the archaeal osmolyte $$ (N (\varepsilon ))(\text( - acetyl - ))\beta (\text( - lysine)) $$ by homologous overexpression of the yodP-kamA genes in Bacillus subtilis.
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- Applied Microbiology & Biotechnology, 2011, v. 91, n. 3, p. 689, doi. 10.1007/s00253-011-3301-8
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- Article
9
Functional analysis of the response regulator DegU in Bacillus megaterium DSM319 and comparative secretome analysis of degSU mutants.
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- Applied Microbiology & Biotechnology, 2011, v. 91, n. 3, p. 699, doi. 10.1007/s00253-011-3302-7
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- Article
10
Hide depilation and feather disintegration studies with keratinolytic serine protease from a novel Bacillus subtilis isolate.
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- Applied Microbiology & Biotechnology, 2008, v. 78, n. 4, p. 643, doi. 10.1007/s00253-008-1355-z
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- Article
11
Cloning, purification, and characterization of chitosanase from Bacillus sp. DAU101.
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- Applied Microbiology & Biotechnology, 2006, v. 73, n. 1, p. 113, doi. 10.1007/s00253-006-0444-0
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- Article
12
Design of a CRISPR-Cas system to increase resistance of Bacillus subtilis to bacteriophage SPP1.
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- Journal of Industrial Microbiology & Biotechnology, 2016, v. 43, n. 8, p. 1183, doi. 10.1007/s10295-016-1784-0
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- Article
13
Engineered Serratia marcescens for efficient (3 R)-acetoin and (2 R,3 R)-2,3-butanediol production.
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- Journal of Industrial Microbiology & Biotechnology, 2015, v. 42, n. 5, p. 779, doi. 10.1007/s10295-015-1598-5
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- Article
14
Overproduction of a thermostable 4-α-glucanotransferase by codon optimization at N-terminus region.
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- Journal of the Science of Food & Agriculture, 2013, v. 93, n. 11, p. 2683, doi. 10.1002/jsfa.6084
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- Article
15
Bacterial sensing: A putative amphipathic helix in RsiV is the switch for activating σ<sup>V</sup> in response to lysozyme.
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- PLoS Genetics, 2018, v. 14, n. 7, p. 1, doi. 10.1371/journal.pgen.1007527
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- Article
16
Antirepression as a second mechanism of transcriptional activation by a minor groove binding protein.
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- Molecular Microbiology, 2007, v. 64, n. 2, p. 368, doi. 10.1111/j.1365-2958.2007.05662.x
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- Article
17
Maturation of the 5′ end of Bacillus subtilis 16S rRNA by the essential ribonuclease YkqC/RNase J1.
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- Molecular Microbiology, 2007, v. 63, n. 1, p. 127, doi. 10.1111/j.1365-2958.2006.05499.x
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- Article
18
Proteolysis of the replication checkpoint protein Sda is necessary for the efficient initiation of sporulation after transient replication stress in Bacillus subtilis.
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- Molecular Microbiology, 2006, v. 60, n. 6, p. 1490, doi. 10.1111/j.1365-2958.2006.05167.x
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- Article
19
StrippingBacillus: ComK auto-stimulation is responsible for the bistable response in competence development.
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- Molecular Microbiology, 2005, v. 56, n. 3, p. 604, doi. 10.1111/j.1365-2958.2005.04488.x
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- Article
20
Functional interplay between theBacillus subtilisDnaD and DnaB proteins essential for initiation and re-initiation of DNA replication.
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- Molecular Microbiology, 2005, v. 55, n. 4, p. 1138, doi. 10.1111/j.1365-2958.2004.04451.x
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- Article
21
Identification of a polar targeting determinant forBacillus subtilisDivIVA.
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- Molecular Microbiology, 2004, v. 54, n. 5, p. 1237, doi. 10.1111/j.1365-2958.2004.04363.x
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- Article
22
Distinctive genetic features exhibited by the Y-family DNA polymerases inBacillus subtilis.
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- Molecular Microbiology, 2004, v. 54, n. 2, p. 439, doi. 10.1111/j.1365-2958.2004.04259.x
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- Article
23
The midcell replication factory inBacillus subtilisis highly mobile: implications for coordinating chromosome replication with other cell cycle events.
- Published in:
- Molecular Microbiology, 2004, v. 54, n. 2, p. 452, doi. 10.1111/j.1365-2958.2004.04267.x
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- Article
24
Identification of additional TnrA-regulated genes of Bacillus subtilis associated with a TnrA box.
- Published in:
- Molecular Microbiology, 2003, v. 49, n. 1, p. 157, doi. 10.1046/j.1365-2958.2003.03567.x
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- Article
25
Spx (YjbD), a negative effector of competence in Bacillus subtilis , enhances ClpC–MecA–ComK interaction.
- Published in:
- Molecular Microbiology, 2002, v. 44, n. 5, p. 1341, doi. 10.1046/j.1365-2958.2002.02963.x
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- Article
26
Antitermination by GlpP, catabolite repression via CcpA and inducer exclusion triggered by P~GlpK dephosphorylation control Bacillus subtilis glpFK expression.
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- Molecular Microbiology, 2002, v. 43, n. 4, p. 1039, doi. 10.1046/j.1365-2958.2002.02800.x
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- Article
27
Genetic analysis of the chromosome segregation protein Spo0J of Bacillus subtilis: evidence for separate domains involved in DNA binding and interactions with Soj protein.
- Published in:
- Molecular Microbiology, 2001, v. 41, n. 3, p. 743, doi. 10.1046/j.1365-2958.2001.02551.x
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28
NucA is required for DNA cleavage during transformation of Bacillus subtilis.
- Published in:
- Molecular Microbiology, 2001, v. 40, n. 3, p. 634, doi. 10.1046/j.1365-2958.2001.02406.x
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29
Replication mutations differentially enhance RecA-dependent and RecA-independent recombination between tandem repeats in Bacillus subtilis.
- Published in:
- Molecular Microbiology, 2001, v. 39, n. 5, p. 1248, doi. 10.1111/j.1365-2958.2001.02312.x
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- Article
30
Expression of the Bacillus subtilis sulphonate–sulphur utilization genes is regulated at the levels of transcription initiation and termination.
- Published in:
- Molecular Microbiology, 2001, v. 39, n. 5, p. 1356, doi. 10.1111/j.1365-2958.2001.02327.x
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31
Catabolite repression mediated by the CcpA protein in Bacillus subtilis: novel modes of regulation revealed by whole-genome analyses.
- Published in:
- Molecular Microbiology, 2001, v. 39, n. 5, p. 1366, doi. 10.1111/j.1365-2958.2001.02328.x
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32
Endoribonuclease RNase III is essential in Bacillus subtilis.
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- Molecular Microbiology, 2000, v. 38, n. 5, p. 1027, doi. 10.1046/j.1365-2958.2000.02185.x
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- Article
33
Mid-cell Z ring assembly in the absence of entry into the elongation phase of the round of replication in bacteria: co-ordinating chromosome replication with cell division.
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- Molecular Microbiology, 2000, v. 38, n. 3, p. 423, doi. 10.1046/j.1365-2958.2000.02130.x
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- Article
34
Divergent structure of the ComQXPA quorum-sensing components: molecular basis of strain-specific communication mechanism in Bacillus subtilis.
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- Molecular Microbiology, 2000, v. 37, n. 5, p. 1159, doi. 10.1046/j.1365-2958.2000.02069.x
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- Article
35
Interaction of ResD with regulatory regions of anaerobically induced genes in Bacillus subtilis.
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- Molecular Microbiology, 2000, v. 37, n. 5, p. 1198, doi. 10.1046/j.1365-2958.2000.02075.x
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- Article
36
ResD signal transduction regulator of aerobic respiration in Bacillus subtilis: ctaA promoter regulation.
- Published in:
- Molecular Microbiology, 2000, v. 37, n. 5, p. 1208, doi. 10.1046/j.1365-2958.2000.02076.x
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- Publication type:
- Article
37
Mutations conferring amino acid residue substitutions in the carboxy-terminal domain of RNA polymerase α can suppress clpX and clpP with respect to developmentally regulated transcription in Bacillus subtilis.
- Published in:
- Molecular Microbiology, 2000, v. 37, n. 4, p. 869, doi. 10.1046/j.1365-2958.2000.02052.x
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38
The N- and C-terminal domains of MecA recognize different partners in the competence molecular switch.
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- Molecular Microbiology, 1999, v. 33, n. 4, p. 886, doi. 10.1046/j.1365-2958.1999.01544.x
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39
Post-transcriptional regulation of the Bacillus subtilis dnaK operon.
- Published in:
- Molecular Microbiology, 1999, v. 32, n. 6, p. 1183, doi. 10.1046/j.1365-2958.1999.01428.x
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- Article
40
σ[supM], an ECF RNA polymerase sigma factor of Bacillus subtilis 168, is essential for growth and survival in high concentrations of salt.
- Published in:
- Molecular Microbiology, 1999, v. 32, n. 1, p. 41, doi. 10.1046/j.1365-2958.1999.01323.x
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41
Autogenous regulation of transcription termination factor Rho and the requirement for Nus factors in Bacillus subtilis.
- Published in:
- Molecular Microbiology, 1999, v. 31, n. 2, p. 651, doi. 10.1046/j.1365-2958.1999.01205.x
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42
Serine kinase activity of a Bacillus subtilis switch protein is required to transduce...
- Published in:
- Molecular Microbiology, 1998, v. 30, n. 1, p. 189, doi. 10.1046/j.1365-2958.1998.01052.x
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43
Transcription-driven DNA replication of plasmid pAMbeta1 in Bacillus subtilis.
- Published in:
- Molecular Microbiology, 1998, v. 30, n. 1, p. 135, doi. 10.1046/j.1365-2958.1998.01044.x
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44
Analysis of the Bacillus subtilis genome sequence reveals nine new T-box leaders.
- Published in:
- Molecular Microbiology, 1998, v. 29, n. 2, p. 662, doi. 10.1046/j.1365-2958.1998.00912.x
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45
A UDP glucosyltransferase from Bacillus subtilis successively transfers up to four glucose residues to 1,2-diacylglycerol: expression ofypfP inEscherichia coli and structural analysis of its reaction products.
- Published in:
- Molecular Microbiology, 1998, v. 29, n. 2, p. 419, doi. 10.1046/j.1365-2958.1998.00930.x
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- Article
46
ClpC regulates the fate of a sporulation initiation sigma factor, σ[sup H] protein, inBacillus subtilis at elevated temperatures.
- Published in:
- Molecular Microbiology, 1998, v. 29, n. 2, p. 505, doi. 10.1046/j.1365-2958.1998.00943.x
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- Publication type:
- Article
47
Characterization of the essential cell division gene ftsL (yllD ) ofBacillus subtilis and its role in the assembly of the division apparatus.
- Published in:
- Molecular Microbiology, 1998, v. 29, n. 2, p. 593, doi. 10.1046/j.1365-2958.1998.00954.x
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48
Osmoregulation of the opuE proline transport gene from Bacilus subtilis: contributions of the...
- Published in:
- Molecular Microbiology, 1998, v. 29, n. 1, p. 285, doi. 10.1046/j.1365-2958.1998.00929.x
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49
PcrA is an essential DNA helicase of Bacillus subtilis fulfilling functions both in...
- Published in:
- Molecular Microbiology, 1998, v. 29, n. 1, p. 261, doi. 10.1046/j.1365-2958.1998.00927.x
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50
Bacillus subtilis contains multiple Fur homologues: identification of theiron uptake (Fur)...
- Published in:
- Molecular Microbiology, 1998, v. 29, n. 1, p. 189, doi. 10.1046/j.1365-2958.1998.00921.x
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- Article