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σ factor

Activation of the Extracytoplasmic Function σ Factor σP by β-Lactams in Bacillus thuringiensis Requires the Site-2 Protease RasP

Activation of the Extracytoplasmic Function σ Factor σP by β-Lactams in Bacillus thuringiensis Requires the Site-2 Protease RasP

... ␴ factor; partner switching, where an anti-anti- ␴ factor frees the ␴ factor from the anti- ␴ factor; or proteolytic destruction of the anti- ␴ factor (9, ...␴ factor at site-1 ...

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BspR/BtrA, an Anti-σ Factor, Regulates the Ability of Bordetella bronchiseptica To Cause Cough in Rats

BspR/BtrA, an Anti-σ Factor, Regulates the Ability of Bordetella bronchiseptica To Cause Cough in Rats

... Rat coughing was not attributable to major virulence factors. It has been often pointed out that a virulence factor(s) involved in cough production should be shared by classical Bordetella, B. pertussis, B. ...

12

Structured and Dynamic Disordered Domains Regulate the Activity of a Multifunctional Anti σ Factor

Structured and Dynamic Disordered Domains Regulate the Activity of a Multifunctional Anti σ Factor

... ␴ factor. In conclusion, our study provides evidence that the anti-␴ factor NepR coordinately utilizes structured and intrin- sically disordered domains to control multiple functions in the ...

11

Regulation of antimycin biosynthesis by the orphan ECF RNA polymerase sigma factor σ (AntA.).

Regulation of antimycin biosynthesis by the orphan ECF RNA polymerase sigma factor σ (AntA.).

... 3-aminosalicylate-CoA (Schoenian et al., 2012; Sandy et al., 2012). The AntCD proteins comprise the hybrid NRPS/PKS machinery, and AntE and AntM are crotonyl-CoA reductase and discrete ketoreductase homologues, ...

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Environmental adaptability and stress tolerance of Laribacter hongkongensis: a genome-wide analysis

Environmental adaptability and stress tolerance of Laribacter hongkongensis: a genome-wide analysis

... -deoxyguanosine; σ 24 (RpoE): RNA polymerase sigma-E factor; σ 28 (FliA): RNA polymerase sigma factor for flagellar operon; σ 32 (RpoH): RNA polymerase sigma-32 factor; σ ...

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Staron, Anna
  

(2012):


	Phylogenetic and functional analyses of stress-responsive bacterial transmembrane signal transducing systems.


Dissertation, LMU München: Fakultät für Biologie

Staron, Anna (2012): Phylogenetic and functional analyses of stress-responsive bacterial transmembrane signal transducing systems. Dissertation, LMU München: Fakultät für Biologie

... alternative σ-factor is closely related to the primary (or vegetative) ...anti-σ factor, in contrast to most other stress-inducible alternative ...

218

Infinite-σ Limits For Tikhonov Regularization

Infinite-σ Limits For Tikhonov Regularization

... κ σ is approximated by the four leading terms in this ...(κ σ (x, x ′ ) ∼ 1 − σ − 2 ( || x || 2 − || x ′ || 2 + 2x · x ′ )/2) does not satisfy the Mercer condition, so the resulting dual ob- jective ...

22

On σ type zero of Sheffer polynomials

On σ type zero of Sheffer polynomials

... Recently Pintér and Srivastava [] gave addition theorems for the Appell polynomials and the associated classes of polynomial expansions and some cases have also been discussed by Srivas[r] ...

9

(L,M) Fuzzy σ Algebras

(L,M) Fuzzy σ Algebras

... fuzzy σ-algebras in 1 in order to prepare a measure theory for fuzzy ...fuzzy σ-algebra X, σ, σ was defined as a crisp family of fuzzy subsets of a set X satisfying certain set of ...fuzzy ...

11

Design of ∆Σ DAC for SAR ADC

Design of ∆Σ DAC for SAR ADC

... The conventional SAR ADC employs a charge distribution capacitive DAC. The limitation of the charge distribution capacitive DAC is that the number of capacitors used for each bit of DAC input. The resolution of DAC which ...

14

Measurement of the cross section ratio σ(χc2)/σ(χc1) for prompt χc production at √s=7 TeV

Measurement of the cross section ratio σ(χc2)/σ(χc1) for prompt χc production at √s=7 TeV

... the σ ( χ c2 )/ σ ( χ c1 ) prompt produc- tion cross-sections has been measured as a function of p T J /ψ using 36 pb − 1 of data collected by LHCb during 2010 at a centre-of-mass energy √ s = 7 ...

10

High Temperature Deformation Behavior of [0001] Symmetrical Tilt Σ 7 and Σ 21 Grain Boundaries in Alumina Bicrystals

High Temperature Deformation Behavior of [0001] Symmetrical Tilt Σ 7 and Σ 21 Grain Boundaries in Alumina Bicrystals

... In this study, relationships between sliding behavior and grain boundary atomic structures were investigated for four types of symmetrical tilt grain boundaries, i.e., 7=f45 10g, 21=f45 [r] ...

6

Present status of the f0(500) or σ meson

Present status of the f0(500) or σ meson

... Thus, the 2012 RPP has finally reduced the uncertainties of the mass, by a factor of more than five, down to 400 to 550 MeV, and width, by a factor of two, now estimated between 400 and 700 MeV. This was ...

5

Borel sets and σ-fragmentability of a Banach space

Borel sets and σ-fragmentability of a Banach space

... T hroughout this thesis two notions will be constantly used. We show th a t cr- fragm entability and having a countable cover by sets of sm all local diam eter are.. W hen ap[r] ...

74

A Note on the Ordinal Analysis of RCA0+WO(σ)

A Note on the Ordinal Analysis of RCA0+WO(σ)

... for some m > 0. There are several ways of obtaining an upper bound for the order-type of ≺ in terms of the length of a cut free deduction of WO(≺) (see e.g. [13, Theorem 23.1], [19, Theorem 3.6], [6, Theorem 2.27]) ...

13

σ-sporadic prime ideals and superficial elements

σ-sporadic prime ideals and superficial elements

... Abstract. Let A be a Noetherian ring, I be an ideal of A and σ be a semi-prime operation, different from the identity map on the set of all ideals of A. Results of Essan proved that the sets of associated prime ...

11

Intercomparison and improvement of two-stream shortwave radiative transfer schemes in Earth system models for a unified treatment of cryospheric surfaces

Intercomparison and improvement of two-stream shortwave radiative transfer schemes in Earth system models for a unified treatment of cryospheric surfaces

... ing the grains are spherical, the SSPs of snow can thus be computed using Mie theory (Wiscombe, 1980) and ice op- tical constants (Warren and Brandt, 2008). In nature, snow grains are not spherical, and many studies have ...

19

Studying particle acceleration from driven magnetic reconnection at the termination shock of a relativistic striped wind using particle-in-cell simulations

Studying particle acceleration from driven magnetic reconnection at the termination shock of a relativistic striped wind using particle-in-cell simulations

... In this paper, we carry out two-dimensional particle-in-cell (PIC) simulations to model the rel- ativistic striped wind interacting with the termination shock near the equatorial plane of obliquely rotating pulsars. The ...

6

Guarantees in with-profit and unitized with-profit life insurance contracts: Fair valuation problem in presence of the default option

Guarantees in with-profit and unitized with-profit life insurance contracts: Fair valuation problem in presence of the default option

... terminal bonus is an increasing function of σ (see Haberman et al., 2003); in this case, the default option looks like a vanilla put option as the policy reserve is not very sensitive to the fund volatility and ...

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Quadrant marked mesh patterns in 132-avoiding permutations III

Quadrant marked mesh patterns in 132-avoiding permutations III

... It is easy to see that as we sum over all the permutations i σ in Sn 132, our choices for the structure for Ai σ will contribute a factor of a−1,b,c,d−n−i a,b,c,d Qi−1,132 x to Qn,132 x,[r] ...

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