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Shotgun proteomic analysis of mulberry dwarf phytoplasma
BACKGROUND: Mulberry dwarf (MD), which is caused by phytoplasma, is one of the most serious infectious diseases of mulberry. Phytoplasmas have been associated with diseases in several hundred plant species. The inability to culture phytoplasmas in vitro has hindered their characterization at the mol...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873370/ https://www.ncbi.nlm.nih.gov/pubmed/20377883 http://dx.doi.org/10.1186/1477-5956-8-20 |
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author | Ji, Xianling Gai, Yingping Lu, Baoyun Zheng, Chengchao Mu, Zhimei |
author_facet | Ji, Xianling Gai, Yingping Lu, Baoyun Zheng, Chengchao Mu, Zhimei |
author_sort | Ji, Xianling |
collection | PubMed |
description | BACKGROUND: Mulberry dwarf (MD), which is caused by phytoplasma, is one of the most serious infectious diseases of mulberry. Phytoplasmas have been associated with diseases in several hundred plant species. The inability to culture phytoplasmas in vitro has hindered their characterization at the molecular level. Though the complete genomes of two phytoplasmas have been published, little information has been obtained about the proteome of phytoplasma. Therefore, the proteomic information of phytoplasmas would be useful to elucidate the functional mechanisms of phytoplasma in many biological processes. RESULTS: MD phytoplasmas, which belong to the 16SrI-B subgroup based on the 16S DNA analysis, were purified from infected tissues using a combination of differential centrifugation and density gradient centrifugation. The expressed proteome of phytoplasma was surveyed by one-dimensional SDS-PAGE and nanocapillary liquid chromatography-tandem mass spectrometry. A total of 209 phytoplasma proteins were unambiguously assigned, including the proteins with the functions of amino acid biosynthesis, cell envelope, cellular processes, energy metabolism, nucleosides and nucleotide metabolism, replication, transcription, translation, transport and binding as well as the proteins with other functions. In addition to these known function proteins, 63 proteins were annotated as hypothetical or conserved hypothetical proteins. CONCLUSIONS: Taken together, a total of 209 phytoplasma proteins have been experimentally verified, representing the most extensive survey of any phytoplasma proteome to date. This study provided a valuable dataset of phytoplasma proteins, and a better understanding of the energy metabolism and virulence mechanisms of MD phytoplasma. |
format | Text |
id | pubmed-2873370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28733702010-05-20 Shotgun proteomic analysis of mulberry dwarf phytoplasma Ji, Xianling Gai, Yingping Lu, Baoyun Zheng, Chengchao Mu, Zhimei Proteome Sci Research BACKGROUND: Mulberry dwarf (MD), which is caused by phytoplasma, is one of the most serious infectious diseases of mulberry. Phytoplasmas have been associated with diseases in several hundred plant species. The inability to culture phytoplasmas in vitro has hindered their characterization at the molecular level. Though the complete genomes of two phytoplasmas have been published, little information has been obtained about the proteome of phytoplasma. Therefore, the proteomic information of phytoplasmas would be useful to elucidate the functional mechanisms of phytoplasma in many biological processes. RESULTS: MD phytoplasmas, which belong to the 16SrI-B subgroup based on the 16S DNA analysis, were purified from infected tissues using a combination of differential centrifugation and density gradient centrifugation. The expressed proteome of phytoplasma was surveyed by one-dimensional SDS-PAGE and nanocapillary liquid chromatography-tandem mass spectrometry. A total of 209 phytoplasma proteins were unambiguously assigned, including the proteins with the functions of amino acid biosynthesis, cell envelope, cellular processes, energy metabolism, nucleosides and nucleotide metabolism, replication, transcription, translation, transport and binding as well as the proteins with other functions. In addition to these known function proteins, 63 proteins were annotated as hypothetical or conserved hypothetical proteins. CONCLUSIONS: Taken together, a total of 209 phytoplasma proteins have been experimentally verified, representing the most extensive survey of any phytoplasma proteome to date. This study provided a valuable dataset of phytoplasma proteins, and a better understanding of the energy metabolism and virulence mechanisms of MD phytoplasma. BioMed Central 2010-04-08 /pmc/articles/PMC2873370/ /pubmed/20377883 http://dx.doi.org/10.1186/1477-5956-8-20 Text en Copyright ©2010 Ji et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Ji, Xianling Gai, Yingping Lu, Baoyun Zheng, Chengchao Mu, Zhimei Shotgun proteomic analysis of mulberry dwarf phytoplasma |
title | Shotgun proteomic analysis of mulberry dwarf phytoplasma |
title_full | Shotgun proteomic analysis of mulberry dwarf phytoplasma |
title_fullStr | Shotgun proteomic analysis of mulberry dwarf phytoplasma |
title_full_unstemmed | Shotgun proteomic analysis of mulberry dwarf phytoplasma |
title_short | Shotgun proteomic analysis of mulberry dwarf phytoplasma |
title_sort | shotgun proteomic analysis of mulberry dwarf phytoplasma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873370/ https://www.ncbi.nlm.nih.gov/pubmed/20377883 http://dx.doi.org/10.1186/1477-5956-8-20 |
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