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NSs Encoded by Groundnut Bud Necrosis Virus Is a Bifunctional Enzyme
Groundnut bud necrosis virus (GBNV), a member of genus Tospovirus in the family Bunyaviridae, infects a large number of leguminosae and solanaceae plants in India. With a view to elucidate the function of nonstructural protein, NSs encoded by the small RNA genome (S RNA), the NSs protein of GBNV- to...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841200/ https://www.ncbi.nlm.nih.gov/pubmed/20305786 http://dx.doi.org/10.1371/journal.pone.0009757 |
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author | Lokesh, Bhushan Rashmi, Panigrahi R. Amruta, Bhat S. Srisathiyanarayanan, Dharmaiah Murthy, Mathur R. N. Savithri, Handanahal S. |
author_facet | Lokesh, Bhushan Rashmi, Panigrahi R. Amruta, Bhat S. Srisathiyanarayanan, Dharmaiah Murthy, Mathur R. N. Savithri, Handanahal S. |
author_sort | Lokesh, Bhushan |
collection | PubMed |
description | Groundnut bud necrosis virus (GBNV), a member of genus Tospovirus in the family Bunyaviridae, infects a large number of leguminosae and solanaceae plants in India. With a view to elucidate the function of nonstructural protein, NSs encoded by the small RNA genome (S RNA), the NSs protein of GBNV- tomato (Karnataka) [1] was over-expressed in E. coli and purified by Ni-NTA chromatography. The purified rNSs protein exhibited an RNA stimulated NTPase activity. Further, this activity was metal ion dependent and was inhibited by adenosine 5′ (β, γ imido) triphosphate, an ATP analog. The rNSs could also hydrolyze dATP. Interestingly, in addition to the NTPase and dATPase activities, the rNSs exhibited ATP independent 5′ RNA/DNA phosphatase activity that was completely inhibited by AMP. The 5′ α phosphate could be removed from ssDNA, ssRNA, dsDNA and dsRNA thus confirming that rNSs has a novel 5′ α phosphatase activity. K189A mutation in the Walker motif A (GxxxxGKT) resulted in complete loss of ATPase activity, but the 5′ phosphatase activity was unaffected. On the other hand, D159A mutation in the Walker motif B (DExx) resulted in partial loss of both the activities. These results demonstrate for the first time that NSs is a bifunctional enzyme, which could participate in viral movement, replication or in suppression of the host defense mechanism. |
format | Text |
id | pubmed-2841200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-28412002010-03-20 NSs Encoded by Groundnut Bud Necrosis Virus Is a Bifunctional Enzyme Lokesh, Bhushan Rashmi, Panigrahi R. Amruta, Bhat S. Srisathiyanarayanan, Dharmaiah Murthy, Mathur R. N. Savithri, Handanahal S. PLoS One Research Article Groundnut bud necrosis virus (GBNV), a member of genus Tospovirus in the family Bunyaviridae, infects a large number of leguminosae and solanaceae plants in India. With a view to elucidate the function of nonstructural protein, NSs encoded by the small RNA genome (S RNA), the NSs protein of GBNV- tomato (Karnataka) [1] was over-expressed in E. coli and purified by Ni-NTA chromatography. The purified rNSs protein exhibited an RNA stimulated NTPase activity. Further, this activity was metal ion dependent and was inhibited by adenosine 5′ (β, γ imido) triphosphate, an ATP analog. The rNSs could also hydrolyze dATP. Interestingly, in addition to the NTPase and dATPase activities, the rNSs exhibited ATP independent 5′ RNA/DNA phosphatase activity that was completely inhibited by AMP. The 5′ α phosphate could be removed from ssDNA, ssRNA, dsDNA and dsRNA thus confirming that rNSs has a novel 5′ α phosphatase activity. K189A mutation in the Walker motif A (GxxxxGKT) resulted in complete loss of ATPase activity, but the 5′ phosphatase activity was unaffected. On the other hand, D159A mutation in the Walker motif B (DExx) resulted in partial loss of both the activities. These results demonstrate for the first time that NSs is a bifunctional enzyme, which could participate in viral movement, replication or in suppression of the host defense mechanism. Public Library of Science 2010-03-18 /pmc/articles/PMC2841200/ /pubmed/20305786 http://dx.doi.org/10.1371/journal.pone.0009757 Text en Lokesh et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Lokesh, Bhushan Rashmi, Panigrahi R. Amruta, Bhat S. Srisathiyanarayanan, Dharmaiah Murthy, Mathur R. N. Savithri, Handanahal S. NSs Encoded by Groundnut Bud Necrosis Virus Is a Bifunctional Enzyme |
title | NSs Encoded by Groundnut Bud Necrosis Virus Is a Bifunctional Enzyme |
title_full | NSs Encoded by Groundnut Bud Necrosis Virus Is a Bifunctional Enzyme |
title_fullStr | NSs Encoded by Groundnut Bud Necrosis Virus Is a Bifunctional Enzyme |
title_full_unstemmed | NSs Encoded by Groundnut Bud Necrosis Virus Is a Bifunctional Enzyme |
title_short | NSs Encoded by Groundnut Bud Necrosis Virus Is a Bifunctional Enzyme |
title_sort | nss encoded by groundnut bud necrosis virus is a bifunctional enzyme |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841200/ https://www.ncbi.nlm.nih.gov/pubmed/20305786 http://dx.doi.org/10.1371/journal.pone.0009757 |
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