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Items: 25

1.

Self-control of the PHO regulon: the PhoP-dependent protein PhoU controls negatively expression of genes of PHO regulon in Streptomyces coelicolor.

Martín-Martín S, Rodríguez-García A, Santos-Beneit F, Franco-Domínguez E, Sola-Landa A, Martín JF.

J Antibiot (Tokyo). 2017 Nov 1. doi: 10.1038/ja.2017.130. [Epub ahead of print]

PMID:
29089595
2.

Intra- and Extra-cellular Proteome Analyses of Steroid-Producer Mycobacteria.

Barreiro C, Morales A, Vázquez-Iglesias I, Sola-Landa A.

Methods Mol Biol. 2017;1645:73-92. doi: 10.1007/978-1-4939-7183-1_6.

PMID:
28710622
3.

RNA-Seq-Based Comparative Transcriptomics: RNA Preparation and Bioinformatics.

Rodríguez-García A, Sola-Landa A, Barreiro C.

Methods Mol Biol. 2017;1645:59-72. doi: 10.1007/978-1-4939-7183-1_5.

PMID:
28710621
4.

Genome Sequencing of Steroid Producing Bacteria Using Ion Torrent Technology and a Reference Genome.

Sola-Landa A, Rodríguez-García A, Barreiro C, Pérez-Redondo R.

Methods Mol Biol. 2017;1645:45-58. doi: 10.1007/978-1-4939-7183-1_4.

PMID:
28710620
5.

Complete genome sequence of 'Mycobacterium neoaurum' NRRL B-3805, an androstenedione (AD) producer for industrial biotransformation of sterols.

Rodríguez-García A, Fernández-Alegre E, Morales A, Sola-Landa A, Lorraine J, Macdonald S, Dovbnya D, Smith MC, Donova M, Barreiro C.

J Biotechnol. 2016 Apr 20;224:64-5. doi: 10.1016/j.jbiotec.2016.03.021. Epub 2016 Mar 14.

PMID:
26988397
6.

Transcriptional control of the F0F1-ATP synthase operon of Corynebacterium glutamicum: SigmaH factor binds to its promoter and regulates its expression at different pH values.

Barriuso-Iglesias M, Barreiro C, Sola-Landa A, Martín JF.

Microb Biotechnol. 2013 Mar;6(2):178-88. doi: 10.1111/1751-7915.12022. Epub 2013 Jan 9.

7.

Competition between the GlnR and PhoP regulators for the glnA and amtB promoters in Streptomyces coelicolor.

Sola-Landa A, Rodríguez-García A, Amin R, Wohlleben W, Martín JF.

Nucleic Acids Res. 2013 Feb 1;41(3):1767-82. doi: 10.1093/nar/gks1203. Epub 2012 Dec 16.

8.

Draft genome of Streptomyces tsukubaensis NRRL 18488, the producer of the clinically important immunosuppressant tacrolimus (FK506).

Barreiro C, Prieto C, Sola-Landa A, Solera E, Martínez-Castro M, Pérez-Redondo R, García-Estrada C, Aparicio JF, Fernández-Martínez LT, Santos-Aberturas J, Salehi-Najafabadi Z, Rodríguez-García A, Tauch A, Martín JF.

J Bacteriol. 2012 Jul;194(14):3756-7. doi: 10.1128/JB.00692-12.

9.

Transcriptomic studies of phosphate control of primary and secondary metabolism in Streptomyces coelicolor.

Martín JF, Santos-Beneit F, Rodríguez-García A, Sola-Landa A, Smith MC, Ellingsen TE, Nieselt K, Burroughs NJ, Wellington EM.

Appl Microbiol Biotechnol. 2012 Jul;95(1):61-75. doi: 10.1007/s00253-012-4129-6. Epub 2012 May 24. Review.

PMID:
22622839
10.

The RNA polymerase omega factor RpoZ is regulated by PhoP and has an important role in antibiotic biosynthesis and morphological differentiation in Streptomyces coelicolor.

Santos-Beneit F, Barriuso-Iglesias M, Fernández-Martínez LT, Martínez-Castro M, Sola-Landa A, Rodríguez-García A, Martín JF.

Appl Environ Microbiol. 2011 Nov;77(21):7586-94. doi: 10.1128/AEM.00465-11. Epub 2011 Sep 9.

11.

Cross-talk of global nutritional regulators in the control of primary and secondary metabolism in Streptomyces.

Martín JF, Sola-Landa A, Santos-Beneit F, Fernández-Martínez LT, Prieto C, Rodríguez-García A.

Microb Biotechnol. 2011 Mar;4(2):165-74. doi: 10.1111/j.1751-7915.2010.00235.x. Epub 2010 Dec 19. Review.

12.

Phosphate control over nitrogen metabolism in Streptomyces coelicolor: direct and indirect negative control of glnR, glnA, glnII and amtB expression by the response regulator PhoP.

Rodríguez-García A, Sola-Landa A, Apel K, Santos-Beneit F, Martín JF.

Nucleic Acids Res. 2009 Jun;37(10):3230-42. doi: 10.1093/nar/gkp162. Epub 2009 Mar 24.

13.

Cross-talk between two global regulators in Streptomyces: PhoP and AfsR interact in the control of afsS, pstS and phoRP transcription.

Santos-Beneit F, Rodríguez-García A, Sola-Landa A, Martín JF.

Mol Microbiol. 2009 Apr;72(1):53-68. doi: 10.1111/j.1365-2958.2009.06624.x. Epub 2009 Feb 11.

14.

Target genes and structure of the direct repeats in the DNA-binding sequences of the response regulator PhoP in Streptomyces coelicolor.

Sola-Landa A, Rodríguez-García A, Apel AK, Martín JF.

Nucleic Acids Res. 2008 Mar;36(4):1358-68. doi: 10.1093/nar/gkm1150. Epub 2008 Jan 10.

15.
16.

Genome-wide transcriptomic and proteomic analysis of the primary response to phosphate limitation in Streptomyces coelicolor M145 and in a DeltaphoP mutant.

Rodríguez-García A, Barreiro C, Santos-Beneit F, Sola-Landa A, Martín JF.

Proteomics. 2007 Jul;7(14):2410-29.

PMID:
17623301
17.
18.

The two-component phoR-phoP system of Streptomyces natalensis: Inactivation or deletion of phoP reduces the negative phosphate regulation of pimaricin biosynthesis.

Mendes MV, Tunca S, Antón N, Recio E, Sola-Landa A, Aparicio JF, Martín JF.

Metab Eng. 2007 Mar;9(2):217-27. Epub 2006 Oct 24.

PMID:
17142079
19.

The lipopolysaccharide of Brucella abortus BvrS/BvrR mutants contains lipid A modifications and has higher affinity for bactericidal cationic peptides.

Manterola L, Moriyón I, Moreno E, Sola-Landa A, Weiss DS, Koch MH, Howe J, Brandenburg K, López-Goñi I.

J Bacteriol. 2005 Aug;187(16):5631-9.

20.

Binding of PhoP to promoters of phosphate-regulated genes in Streptomyces coelicolor: identification of PHO boxes.

Sola-Landa A, Rodríguez-García A, Franco-Domínguez E, Martín JF.

Mol Microbiol. 2005 Jun;56(5):1373-85.

21.

The two-component PhoR-PhoP system controls both primary metabolism and secondary metabolite biosynthesis in Streptomyces lividans.

Sola-Landa A, Moura RS, Martín JF.

Proc Natl Acad Sci U S A. 2003 May 13;100(10):6133-8. Epub 2003 May 2.

22.

Regulation of Brucella virulence by the two-component system BvrR/BvrS.

López-Goñi I, Guzmán-Verri C, Manterola L, Sola-Landa A, Moriyón I, Moreno E.

Vet Microbiol. 2002 Dec 20;90(1-4):329-39. Review.

PMID:
12414153
23.

The two-component system BvrR/BvrS essential for Brucella abortus virulence regulates the expression of outer membrane proteins with counterparts in members of the Rhizobiaceae.

Guzman-Verri C, Manterola L, Sola-Landa A, Parra A, Cloeckaert A, Garin J, Gorvel JP, Moriyon I, Moreno E, Lopez-Goni I.

Proc Natl Acad Sci U S A. 2002 Sep 17;99(19):12375-80. Epub 2002 Sep 6.

24.

Brucella abortus transits through the autophagic pathway and replicates in the endoplasmic reticulum of nonprofessional phagocytes.

Pizarro-Cerdá J, Méresse S, Parton RG, van der Goot G, Sola-Landa A, Lopez-Goñi I, Moreno E, Gorvel JP.

Infect Immun. 1998 Dec;66(12):5711-24.

25.

A two-component regulatory system playing a critical role in plant pathogens and endosymbionts is present in Brucella abortus and controls cell invasion and virulence.

Sola-Landa A, Pizarro-Cerdá J, Grilló MJ, Moreno E, Moriyón I, Blasco JM, Gorvel JP, López-Goñi I.

Mol Microbiol. 1998 Jul;29(1):125-38.

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