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1.
Sci Rep ; 9(1): 13136, 2019 09 11.
Artigo em Inglês | MEDLINE | ID: mdl-31511549

RESUMO

Carotenoid production in some non-phototropic bacteria occurs in a light-dependent manner to protect cells from photo-oxidants. Knowledge regarding the transcriptional regulator involved in the light-dependent production of carotenoids of non-phototrophic bacteria has been mainly confined to coenzyme B12-based photo-sensitive regulator CarH/LitR family proteins belonging to a MerR family transcriptional regulator. In this study, we found that bacteria belonging to Micrococcales and Corynebacteriales exhibit light-dependent carotenoid-like pigment production including an amino acid-producer Corynebacterium glutamicum AJ1511. CrtR is a putative MarR family transcriptional regulator located in the divergent region of a carotenoid biosynthesis gene cluster in the genome of those bacteria. A null mutant for crtR of C. glutamicum AJ1511 exhibited constitutive production of carotenoids independent of light. A complemented strain of the crtR mutant produced carotenoids in a light-dependent manner. Transcriptional analysis revealed that the expression of carotenoid biosynthesis genes is regulated in a light-dependent manner in the wild type, while the transcription was upregulated in the crtR mutant irrespective of light. In vitro experiments demonstrated that a recombinant CrtR protein binds to the specific sequences within the intergenic region of crtR and crtE, which corresponds to -58 to -7 for crtE, and +26 to -28 for crtR with respect to the transcriptional start site, and serves as a repressor for crtE transcription directed by RNA polymerase containing SigA. Taken together, the results indicate that CrtR light-dependently controls the expression of the carotenoid gene cluster in C. glutamicum and probably closely related Actinobacteria.


Assuntos
Proteínas de Bactérias/genética , Carotenoides/metabolismo , Corynebacterium glutamicum/genética , Regulação Bacteriana da Expressão Gênica/efeitos da radiação , Luz , Transcrição Gênica/efeitos da radiação , Sequência de Aminoácidos , Proteínas de Bactérias/metabolismo , Sequência de Bases , Corynebacterium glutamicum/metabolismo , Família Multigênica/genética , Regiões Promotoras Genéticas/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Sítio de Iniciação de Transcrição
2.
Microbiology (Reading) ; 162(8): 1500-1509, 2016 08.
Artigo em Inglês | MEDLINE | ID: mdl-27283316

RESUMO

The LitR/CarH protein family transcriptional regulator is a new type of photoreceptor based on the function of adenosyl B12 (AdoB12) as a light-sensitive ligand. Here, we studied a semi-conserved histidine residue (His132) in the light-sensing (AdoB12-binding) domain at the C-terminus of LitR from a thermophilic Gram-negative bacterium, Thermus thermophilus HB27. The in vivo mutation of His132 within LitR caused a reduction in the rate of carotenoid production in response to illumination. BIAcore analysis revealed that the illuminated-LitRH132A possesses high DNA-binding activity compared to the wild-type protein. The subunit structure analysis showed that LitRH132A performed an incomplete subunit dissociation. The ability of LitRH132A to associate with AdoB12 was reduced compared with that of the wild-type protein in an equilibration dialysis experiment. Overall, these results suggest that His132 of LitR is involved in the association with AdoB12 as well as the light-sensitive DNA-binding activity based on oligomer dissociation.


Assuntos
Proteínas de Bactérias/genética , Proteínas de Ligação a DNA/genética , Histidina/genética , Fotorreceptores Microbianos/genética , Thermus thermophilus/genética , Thermus thermophilus/fisiologia , Sequência de Aminoácidos/genética , Regulação Bacteriana da Expressão Gênica , Luz , Mutação/genética , Regiões Promotoras Genéticas/genética , Alinhamento de Sequência , Transcrição Gênica/genética
3.
J Bacteriol ; 197(14): 2301-15, 2015 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-25917914

RESUMO

UNLABELLED: The LitR/CarH family of proteins is a light-sensitive MerR family of transcriptional regulators that contain an adenosyl B12 (coenzyme B12 or AdoB12)-binding domain at the C terminus. The genes encoding these proteins are found in phylogenetically diverse bacterial genera; however, the biochemical properties of these proteins from Gram-positive bacteria remain poorly understood. We performed genetic and biochemical analyses of a homolog of the LitR protein from Bacillus megaterium QM B1551, a Gram-positive endospore-forming soil bacterium. Carotenoid production was induced by illumination in this bacterium. In vivo analysis demonstrated that LitR plays a central role in light-inducible carotenoid production and serves as a negative regulator of the light-inducible transcription of crt and litR itself. Biochemical evidence showed that LitR in complex with AdoB12 binds to the promoter regions of litR and the crt operon in a light-sensitive manner. In vitro transcription experiments demonstrated that AdoB12-LitR inhibited the specific transcription of the crt promoter generated by a σ(A)-containing RNA polymerase holoenzyme under dark conditions. Collectively, these data indicate that the AdoB12-LitR complex serves as a photoreceptor with DNA-binding activity in B. megaterium QM B1551 and that its function as a transcriptional repressor is fundamental to the light-induced carotenoid production. IMPORTANCE: Members of the LitR/CarH family are AdoB12-based photosensors involved in light-inducible carotenoid production in nonphototrophic Gram-negative bacteria. Our study revealed that Bacillus LitR in complex with AdoB12 also serves as a transcriptional regulator with a photosensory function, which indicates that the LitR/CarH family is generally involved in the light-inducible carotenoid production of nonphototrophic bacteria.


Assuntos
Bacillus megaterium/metabolismo , Proteínas de Bactérias/metabolismo , Carotenoides/metabolismo , Cobamidas/metabolismo , Regulação Bacteriana da Expressão Gênica/fisiologia , Sequência de Aminoácidos , Bacillus megaterium/genética , Sequência de Bases , Sítios de Ligação , Cobamidas/química , Pegada de DNA , Desoxirribonuclease I/metabolismo , Luz , Dados de Sequência Molecular , Regiões Promotoras Genéticas , Ligação Proteica
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