-
Je něco špatně v tomto záznamu ?
Intracellular sequestration of cadmium and zinc in ectomycorrhizal fungus Amanita muscaria (Agaricales, Amanitaceae) and characterization of its metallothionein gene
S. Jan, C. Anna, K. Antonín, Š. Jiří, B. Jan, L. Tereza, K. Pavel
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
- MeSH
- Amanita genetika metabolismus MeSH
- kadmium metabolismus MeSH
- měď metabolismus MeSH
- metalothionein * genetika metabolismus MeSH
- mykorhiza * genetika MeSH
- Saccharomyces cerevisiae metabolismus MeSH
- zinek metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
Amanita muscaria is an ectomycorrhizal mushroom that commonly grows at metal-polluted sites. Sporocarps from the lead smelter-polluted area near Příbram (Central Bohemia, Czech Republic) showed elevated concentrations of Cd and Zn. Size exclusion chromatography of the cell extracts of the sporocarps from both polluted and unpolluted sites indicated that substantial part of intracellular Cd and Zn was sequestered in 6-kDa complexes, presumably with metallothionein(s) (MT). When the cultured mycelial isolates were compared, those from Příbram were more Cd-tolerant and accumulated slightly less Cd and Zn than those from the unpolluted site. The analysis of the available A.muscaria sequence data returned a 67-amino acid (AA) MT encoded by the AmMT1 gene. Weak Cd and Zn responsiveness of AmMT1 in the mycelia suggested its metal homeostasis function in A.muscaria, rather than a major role in detoxification. The AmMT1 belongs to a ubiquitous peptide group in the Agaricomycetes consisting of 60-70-AA MTs containing seven cysteinyl domains and a conserved histidyl, features observed also in a newly predicted, atypical 45-AA RaMT1 of the Zn-accumulator Russula bresadolae in which the C-terminal cysteinyl domains VI and VII are missing. Heterologous expression in metal-sensitive yeast mutants indicated that AmMT1 and RaMT1 encode functional peptides that can protect cells against Cd, Zn, and Cu toxicity. The metal protection phenotype observed in yeasts with mutant variants of AmMT1 and RaMT1 further indicated that the conserved histidyl seems to play a structural, not metal binding role, and the cysteinyls of the C-terminal domains VI and VII are important for Cu binding. The data provide an important insight into the metal handling of site-associated ectomycorrhizal species disturbed by excess metals and the properties of MTs common in Agaricomycetes.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc22024579
- 003
- CZ-PrNML
- 005
- 20221031100854.0
- 007
- ta
- 008
- 221017s2022 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.fgb.2022.103717 $2 doi
- 035 __
- $a (PubMed)35764233
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Jan, Sácký $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Prague, Technická 3, 166 28 Prague 6, Czech Republic
- 245 10
- $a Intracellular sequestration of cadmium and zinc in ectomycorrhizal fungus Amanita muscaria (Agaricales, Amanitaceae) and characterization of its metallothionein gene / $c S. Jan, C. Anna, K. Antonín, Š. Jiří, B. Jan, L. Tereza, K. Pavel
- 520 9_
- $a Amanita muscaria is an ectomycorrhizal mushroom that commonly grows at metal-polluted sites. Sporocarps from the lead smelter-polluted area near Příbram (Central Bohemia, Czech Republic) showed elevated concentrations of Cd and Zn. Size exclusion chromatography of the cell extracts of the sporocarps from both polluted and unpolluted sites indicated that substantial part of intracellular Cd and Zn was sequestered in 6-kDa complexes, presumably with metallothionein(s) (MT). When the cultured mycelial isolates were compared, those from Příbram were more Cd-tolerant and accumulated slightly less Cd and Zn than those from the unpolluted site. The analysis of the available A.muscaria sequence data returned a 67-amino acid (AA) MT encoded by the AmMT1 gene. Weak Cd and Zn responsiveness of AmMT1 in the mycelia suggested its metal homeostasis function in A.muscaria, rather than a major role in detoxification. The AmMT1 belongs to a ubiquitous peptide group in the Agaricomycetes consisting of 60-70-AA MTs containing seven cysteinyl domains and a conserved histidyl, features observed also in a newly predicted, atypical 45-AA RaMT1 of the Zn-accumulator Russula bresadolae in which the C-terminal cysteinyl domains VI and VII are missing. Heterologous expression in metal-sensitive yeast mutants indicated that AmMT1 and RaMT1 encode functional peptides that can protect cells against Cd, Zn, and Cu toxicity. The metal protection phenotype observed in yeasts with mutant variants of AmMT1 and RaMT1 further indicated that the conserved histidyl seems to play a structural, not metal binding role, and the cysteinyls of the C-terminal domains VI and VII are important for Cu binding. The data provide an important insight into the metal handling of site-associated ectomycorrhizal species disturbed by excess metals and the properties of MTs common in Agaricomycetes.
- 650 _2
- $a Amanita $x genetika $x metabolismus $7 D000545
- 650 _2
- $a kadmium $x metabolismus $7 D002104
- 650 _2
- $a měď $x metabolismus $7 D003300
- 650 12
- $a metalothionein $x genetika $x metabolismus $7 D008668
- 650 12
- $a mykorhiza $x genetika $7 D038821
- 650 _2
- $a Saccharomyces cerevisiae $x metabolismus $7 D012441
- 650 _2
- $a zinek $x metabolismus $7 D015032
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Anna, Chaloupecká $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Prague, Technická 3, 166 28 Prague 6, Czech Republic
- 700 1_
- $a Antonín, Kaňa $u Department of Analytical Chemistry, University of Chemistry and Technology, Prague, Technická 5, 166 28 Prague, Czech Republic
- 700 1_
- $a Jiří, Šantrůček $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Prague, Technická 3, 166 28 Prague 6, Czech Republic
- 700 1_
- $a Jan, Borovička $u Institute of Geology of the Czech Academy of Sciences, Rozvojová 269, 16500 Prague 6, Czech Republic; Nuclear Physics Institute of the Czech Academy of Sciences, Hlavní 130, 25068 Husinec-Řež, Czech Republic
- 700 1_
- $a Tereza, Leonhardt $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Prague, Technická 3, 166 28 Prague 6, Czech Republic
- 700 1_
- $a Pavel, Kotrba $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Prague, Technická 3, 166 28 Prague 6, Czech Republic. Electronic address: pavel.kotrba@vscht.cz
- 773 0_
- $w MED00001867 $t Fungal genetics and biology $x 1096-0937 $g Roč. 162, č. - (2022), s. 103717
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/35764233 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20221017 $b ABA008
- 991 __
- $a 20221031100851 $b ABA008
- 999 __
- $a ok $b bmc $g 1854352 $s 1175869
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2022 $b 162 $c - $d 103717 $e 20220625 $i 1096-0937 $m Fungal genetics and biology $n Fungal Genet Biol $x MED00001867
- LZP __
- $a Pubmed-20221017