Logotipo do repositório
 

Publicação:
Genome mining for peptidases in heat-tolerant and mesophilic fungi and putative adaptations for thermostability

dc.contributor.authorde Oliveira, Tássio Brito [UNESP]
dc.contributor.authorGostinčar, Cene
dc.contributor.authorGunde-Cimerman, Nina
dc.contributor.authorRodrigues, Andre [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionBiotechnical Faculty
dc.date.accessioned2018-12-11T17:18:14Z
dc.date.available2018-12-11T17:18:14Z
dc.date.issued2018-02-20
dc.description.abstractBackground: Peptidases (EC 3.4) consist of a large group of hydrolytic enzymes that catalyze the hydrolysis of proteins accounting for approximately 65% of the total worldwide enzyme production. Peptidases from thermophilic fungi have adaptations to high temperature that makes them adequate for biotechnological application. In the present study, we profiled the genomes of heat-tolerant fungi and phylogenetically related mesophilic species for genes encoding for peptidases and their putative adaptations for thermostability. Results: We generated an extensive catalogue of these enzymes ranging from 241 to 820 peptidase genes in the genomes of 23 fungi. Thermophilic species presented the smallest number of peptidases encoding genes in relation to mesophilic species, and the peptidases families with a greater number of genes were the most affected. We observed differences in peptidases in thermophilic species in comparison to mesophilic counterparts, at (i) the genome level: a great reduction in the number of peptidases encoding genes that harbored a higher number of copies; (ii) in the primary protein structure: shifts in proportion of single or groups of amino acids; and (iii) in the three-dimensional structure: reduction in the number of internal cavities. Similar results were reported for extremely thermophilic proteins, but here we show for the first time that several changes also occurred on the moderate thermophilic enzymes of fungi. In regards to the amino acids composition, peptidases from thermophilic species in relation to the mesophilic ones, contained a larger proportion of Ala, Glu, Gly, Pro, Arg and Val residues and a lower number of Cys, His, Ile, Lys, Met, Asn, Gln, Ser, Thr and Trp residues(P<0.05). Moreover, we observed an increase in the proportion of hydrophobic and charged amino acids and a decrease in polar amino acids. Conclusions: Although thermophilic fungi present less genes encoding for peptidases, these have adaptations that could play a role in thermal resistance from genome to protein structure level.en
dc.description.affiliationSão Paulo State University (UNESP) Department of Biochemistry and Microbiology, Avenida 24-A, 1515, Bela Vista
dc.description.affiliationUniversity of Ljubljana Department of Biology Biotechnical Faculty
dc.description.affiliationUnespSão Paulo State University (UNESP) Department of Biochemistry and Microbiology, Avenida 24-A, 1515, Bela Vista
dc.identifierhttp://dx.doi.org/10.1186/s12864-018-4549-5
dc.identifier.citationBMC Genomics, v. 19, n. 1, 2018.
dc.identifier.doi10.1186/s12864-018-4549-5
dc.identifier.file2-s2.0-85042527553.pdf
dc.identifier.issn1471-2164
dc.identifier.scopus2-s2.0-85042527553
dc.identifier.urihttp://hdl.handle.net/11449/175937
dc.language.isoeng
dc.relation.ispartofBMC Genomics
dc.relation.ispartofsjr2,110
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectEnzyme
dc.subjectEvolution
dc.subjectModeling
dc.subjectProtease
dc.subjectThermophilic fungi
dc.subjectThermotolerant fungi
dc.titleGenome mining for peptidases in heat-tolerant and mesophilic fungi and putative adaptations for thermostabilityen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.lattes8538509657578022[4]
unesp.author.orcid0000-0002-4164-9362[4]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Rio Claropt
unesp.departmentBioquímica e Microbiologia - IBpt

Arquivos

Pacote Original

Agora exibindo 1 - 1 de 1
Carregando...
Imagem de Miniatura
Nome:
2-s2.0-85042527553.pdf
Tamanho:
749.2 KB
Formato:
Adobe Portable Document Format
Descrição: