Characterization of two genes encoding metal tolerance proteins from Beta vulgaris subspecies maritima that confers manganese tolerance in yeast

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Characterization of two genes encoding metal tolerance proteins from Beta vulgaris subspecies maritima that confers manganese tolerance in yeast. / Erbasol, Isil; Bozdag, Gonensin Ozan; Koc, Ahmet; Pedas, Pai; Karakaya, Huseyin Caglar.

In: BioMetals, Vol. 26, No. 5, 2013, p. 795-804.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Erbasol, I, Bozdag, GO, Koc, A, Pedas, P & Karakaya, HC 2013, 'Characterization of two genes encoding metal tolerance proteins from Beta vulgaris subspecies maritima that confers manganese tolerance in yeast', BioMetals, vol. 26, no. 5, pp. 795-804. https://doi.org/10.1007/s10534-013-9658-7

APA

Erbasol, I., Bozdag, G. O., Koc, A., Pedas, P., & Karakaya, H. C. (2013). Characterization of two genes encoding metal tolerance proteins from Beta vulgaris subspecies maritima that confers manganese tolerance in yeast. BioMetals, 26(5), 795-804. https://doi.org/10.1007/s10534-013-9658-7

Vancouver

Erbasol I, Bozdag GO, Koc A, Pedas P, Karakaya HC. Characterization of two genes encoding metal tolerance proteins from Beta vulgaris subspecies maritima that confers manganese tolerance in yeast. BioMetals. 2013;26(5):795-804. https://doi.org/10.1007/s10534-013-9658-7

Author

Erbasol, Isil ; Bozdag, Gonensin Ozan ; Koc, Ahmet ; Pedas, Pai ; Karakaya, Huseyin Caglar. / Characterization of two genes encoding metal tolerance proteins from Beta vulgaris subspecies maritima that confers manganese tolerance in yeast. In: BioMetals. 2013 ; Vol. 26, No. 5. pp. 795-804.

Bibtex

@article{f61fa69c66344100a74a1d771067182c,
title = "Characterization of two genes encoding metal tolerance proteins from Beta vulgaris subspecies maritima that confers manganese tolerance in yeast",
abstract = "Manganese (Mn) is an essential micronutrient in plants. However increased Mn levels are toxic to plant cells. Metal tolerance proteins (MTPs), member of cation diffusion facilitator protein (CDF) family, have important roles in metal homeostatis in different plant species and catalyse efflux of excess metal ions. In this study, we identified and characterized two MTP genes from Beta vulgaris spp. maritima (B. v. ssp. maritima). Overexpression of these two genes provided Mn tolerance in yeast cells. Sequence analyses displayed BmMTP10 and BmMTP11as members of the Mn-CDF family. Functional analyses of these proteins indicated that they are specific to Mn with a role in reducing excess cellular Mn levels when expressed in yeast. GFP-fusion constructs of both proteins localized to the Golgi apparatus as a punctuated pattern. Finally, Q-RT-PCR results showed that BmMTP10 expression was induced threefold in response to the excess Mn treatment. On the other hand BmMTP11 expression was not affected in response to excess Mn levels. Thus, our results suggest that the BmMTP10 and BmMTP11 proteins from B. v. ssp. maritima have non-redundant functions in terms of Mn detoxification with a similar in planta localization and function as the Arabidopsis Mn-CDF homolog AtMTP11 and this conservation shows the evolutionary importance of these vesicular proteins in heavy metal homeostatis among plant species.",
author = "Isil Erbasol and Bozdag, {Gonensin Ozan} and Ahmet Koc and Pai Pedas and Karakaya, {Huseyin Caglar}",
year = "2013",
doi = "10.1007/s10534-013-9658-7",
language = "English",
volume = "26",
pages = "795--804",
journal = "BioMetals",
issn = "0966-0844",
publisher = "Springer",
number = "5",

}

RIS

TY - JOUR

T1 - Characterization of two genes encoding metal tolerance proteins from Beta vulgaris subspecies maritima that confers manganese tolerance in yeast

AU - Erbasol, Isil

AU - Bozdag, Gonensin Ozan

AU - Koc, Ahmet

AU - Pedas, Pai

AU - Karakaya, Huseyin Caglar

PY - 2013

Y1 - 2013

N2 - Manganese (Mn) is an essential micronutrient in plants. However increased Mn levels are toxic to plant cells. Metal tolerance proteins (MTPs), member of cation diffusion facilitator protein (CDF) family, have important roles in metal homeostatis in different plant species and catalyse efflux of excess metal ions. In this study, we identified and characterized two MTP genes from Beta vulgaris spp. maritima (B. v. ssp. maritima). Overexpression of these two genes provided Mn tolerance in yeast cells. Sequence analyses displayed BmMTP10 and BmMTP11as members of the Mn-CDF family. Functional analyses of these proteins indicated that they are specific to Mn with a role in reducing excess cellular Mn levels when expressed in yeast. GFP-fusion constructs of both proteins localized to the Golgi apparatus as a punctuated pattern. Finally, Q-RT-PCR results showed that BmMTP10 expression was induced threefold in response to the excess Mn treatment. On the other hand BmMTP11 expression was not affected in response to excess Mn levels. Thus, our results suggest that the BmMTP10 and BmMTP11 proteins from B. v. ssp. maritima have non-redundant functions in terms of Mn detoxification with a similar in planta localization and function as the Arabidopsis Mn-CDF homolog AtMTP11 and this conservation shows the evolutionary importance of these vesicular proteins in heavy metal homeostatis among plant species.

AB - Manganese (Mn) is an essential micronutrient in plants. However increased Mn levels are toxic to plant cells. Metal tolerance proteins (MTPs), member of cation diffusion facilitator protein (CDF) family, have important roles in metal homeostatis in different plant species and catalyse efflux of excess metal ions. In this study, we identified and characterized two MTP genes from Beta vulgaris spp. maritima (B. v. ssp. maritima). Overexpression of these two genes provided Mn tolerance in yeast cells. Sequence analyses displayed BmMTP10 and BmMTP11as members of the Mn-CDF family. Functional analyses of these proteins indicated that they are specific to Mn with a role in reducing excess cellular Mn levels when expressed in yeast. GFP-fusion constructs of both proteins localized to the Golgi apparatus as a punctuated pattern. Finally, Q-RT-PCR results showed that BmMTP10 expression was induced threefold in response to the excess Mn treatment. On the other hand BmMTP11 expression was not affected in response to excess Mn levels. Thus, our results suggest that the BmMTP10 and BmMTP11 proteins from B. v. ssp. maritima have non-redundant functions in terms of Mn detoxification with a similar in planta localization and function as the Arabidopsis Mn-CDF homolog AtMTP11 and this conservation shows the evolutionary importance of these vesicular proteins in heavy metal homeostatis among plant species.

UR - http://www.scopus.com/inward/record.url?scp=84885484358&partnerID=8YFLogxK

U2 - 10.1007/s10534-013-9658-7

DO - 10.1007/s10534-013-9658-7

M3 - Journal article

C2 - 23864431

AN - SCOPUS:84885484358

VL - 26

SP - 795

EP - 804

JO - BioMetals

JF - BioMetals

SN - 0966-0844

IS - 5

ER -

ID: 102106538