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Showing papers by "Marcello Pinti published in 1999"


Journal ArticleDOI
TL;DR: It is found that TouR responds to mono- and dimethylphenols, but not the corresponding methylbenzenes, in this respect, the regulation of theP.
Abstract: Toluene–o-xylene monooxygenase is an enzymatic complex, encoded by the touABCDEF genes, responsible for the early stages of toluene and o-xylene degradation in Pseudomonas stutzeri OX1. In order to identify the loci involved in the transcriptional regulation of the tou gene cluster, deletion analysis and complementation studies were carried out with Pseudomonas putida PaW340 as a heterologous host harboring pFB1112, a plasmid that allowed regulated expression, inducible by toluene and o-xylene and their corresponding phenols, of the toluene–o-xylene monooxygenase. A locus encoding a positive regulator, designated touR, was mapped downstream from the tou gene cluster. TouR was found to be similar to transcriptional activators of aromatic compound catabolic pathways belonging to the NtrC family and, in particular, to DmpR (83% similarity), which controls phenol catabolism. By using a touA-C2,3O fusion reporter system and by primer extension analysis, a TouR cognate promoter (PToMO) was mapped, which showed the typical −24 TGGC, −12 TTGC sequences characteristic of ς54-dependent promoters and putative upstream activating sequences. By using the reporter system described, we found that TouR responds to mono- and dimethylphenols, but not the corresponding methylbenzenes. In this respect, the regulation of the P. stutzeri system differs from that of other toluene or xylene catabolic systems, in which the hydrocarbons themselves function as effectors. Northern analyses indicated low transcription levels of tou structural genes in the absence of inducers. Basal toluene–o-xylene monooxygenase activity may thus transform these compounds to phenols, which then trigger the TouR-mediated response.

49 citations


Journal ArticleDOI
TL;DR: In cells of lymphoid origin (ACH‐2) chronic HIV infection inhibits the expression of CD95L, the phenomenon occurring at the transcriptional level, which suggests that HIV could trigger different anti‐apoptotic strategies which likely depend upon the cell line which is infected.

19 citations


Journal ArticleDOI
TL;DR: The data suggest a possible (indirect?) action of antiretroviral therapies on PBG and PBM which could explain, at least partially, the rescue of natural immunity and the reduced use of granulocyte-colony stimulating factor during such treatments.

15 citations