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1.
Microbiol Resour Announc ; 13(1): e0108623, 2024 Jan 17.
Article in English | MEDLINE | ID: mdl-38099681

ABSTRACT

We report the genome sequences of 31 mycobacteriophages isolated on Mycobacterium smegmatis mc2155 at room temperature. The genomes add to the diversity of Clusters A, B, C, G, and K. Collectively, the genomes include 70 novel protein-coding genes that have no close relatives among the actinobacteriophages.

2.
Microbiol Resour Announc ; 11(5): e0018522, 2022 May 19.
Article in English | MEDLINE | ID: mdl-35384701

ABSTRACT

Four microbacteriophages infecting the host Microbacterium foliorum were isolated at Gonzaga University as part of the SEA-PHAGES program. Phages Teehee, StrawberryJamm, Quammi, and Casend are in the EG cluster, with average genome sizes of 62,263 bp and GC contents of 67.2%, with other interesting characteristics.

3.
Genome Announc ; 5(16)2017 Apr 20.
Article in English | MEDLINE | ID: mdl-28428316

ABSTRACT

Mycobacteriophages DrHayes, Urkel, and SamuelLPlaqson were isolated from soil samples in Spokane, WA, using Mycobacterium smegmatis mc2155 grown at room temperature. The three genomes differ by only a few nucleotides, are 60,526 bp long, have 97 predicted protein-coding genes and one tRNA gene, and are members of subcluster K1.

4.
J Biol Chem ; 277(10): 7905-12, 2002 Mar 08.
Article in English | MEDLINE | ID: mdl-11756444

ABSTRACT

Cutin monomers, generated by the low levels of constitutively expressed cutinase, induce high levels of cutinase that can help pathogenic fungi to penetrate into the host through the cuticle whose major structural polymer is cutin. We cloned three highly homologous cutinase genes, cut1, cut2, and cut3, from Fusarium solani f. pisi (Nectria haematococca). Amino acid sequence deduced from the nucleotide sequence of cut1 and cut2/3 matched with that of the peptides from cutinase 1 and cutinase 2, respectively, isolated from F. solani pisi grown on cutin as the sole carbon source. Induction of beta-glucuronidase gene fused to the promoters of the cutinases integrated into F. solani pisi genome indicates that cut2 is constitutively expressed and induced under starvation, whereas cut1 is highly induced by cutin monomers. A palindrome binding protein (PBP) previously cloned binds only to palindrome 1 of cut1 promoter but not palindrome 1 of cut2/3 which contains two base substitutions. PBP is thought to interfere with the binding of CTF1 alpha, the transcription factor involved in induction, to cut1 promoter and thus keep cut1 gene repressed until induced by cutin monomers. Because PBP cannot bind palindrome 1 of cut2, this gene is not repressed. CTF1 alpha does not transactivate cut2 promoter. A new Cys(6)Zn(2) motif-containing transcription factor, CTF1 beta, that binds palindrome 2 was cloned and sequenced. In yeast, CTF1 beta transactivates cut2 promoter but not cut1 promoter unless its palindrome 1 is mutated, unlike CTF1 alpha which transactivates cut1. Thus, CTF1 beta is involved in the constitutive expression of cut2 that causes production of low levels of cutin monomers that strongly induce cut1 using CTF1 alpha as the transcription factor.


Subject(s)
Carboxylic Ester Hydrolases/biosynthesis , Carboxylic Ester Hydrolases/genetics , Fusarium/enzymology , Gene Expression Regulation, Enzymologic , Amino Acid Sequence , Base Sequence , Blotting, Southern , Carboxylic Ester Hydrolases/metabolism , Cloning, Molecular , DNA/metabolism , Gene Library , Glucuronidase/metabolism , Membrane Lipids/metabolism , Models, Biological , Molecular Sequence Data , Plasmids/metabolism , Promoter Regions, Genetic , Protein Binding , Recombinant Proteins/metabolism , Sequence Analysis, DNA , Sequence Homology, Amino Acid , Sequence Homology, Nucleic Acid , Transcriptional Activation , Zinc Fingers
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