Leaf metabolite profile of the Brazilian resurrection plant Barbacenia purpurea Hook. (Velloziaceae) shows two time-dependent responses during desiccation and recovering
Barbacenia purpurea is a resurrection species endemic to rock outcrops, in Rio de Janeiro, Brazil. It tolerates great temperature variations, which are associated to periods of up to 30 days without precipitation. Using a metabolomic approach, we analyzed, under winter and summer conditions, changes...
Saved in:
Published in | Frontiers in plant science Vol. 5; p. 96 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
14.03.2014
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Barbacenia purpurea is a resurrection species endemic to rock outcrops, in Rio de Janeiro, Brazil. It tolerates great temperature variations, which are associated to periods of up to 30 days without precipitation. Using a metabolomic approach, we analyzed, under winter and summer conditions, changes in the leaf metabolite profile (MP) of potted plants of B. purpurea submitted to daily watered and water deficit for at least 20 days and subsequent slow rehydration for 5 days. Leaves were collected at different time points and had their MP analyzed by GC/MS, HPAEC, and UHPLC techniques, allowing the identification of more than 60 different compounds, including organic and amino acids, sugars, and polyols, among others. In the winter experiment, results suggest the presence of two time-dependent responses in B. purpurea under water stress. The first one starts with the increase in the content of caffeoyl-quinic acids, substances with strong antioxidant activity, until the 16th day of water suppression. When RWC reached less than 80 and 70%, in winter and summer respectively, it was observed an increase in polyols and monosaccharides, followed by an increment in the content of RFO, suggesting osmotic adjustment. Amino acids, such as GABA and asparagine, also increased due to 16 days of water suppression. During rehydration, the levels of the mentioned compounds became similar to those found at the beginning of the experiment and when compared to daily watered plants. We conclude that the tolerance of B. purpurea to dehydration involves the perception of water deficit intensity, which seems to result in different strategies to overcome the gradient of water availability imposed along a certain period of stress mainly during winter. Data from summer experiment indicate that the metabolism of B. pupurea was already primed for drought stress. The accumulation of phenolics in summer seemed to be more temperature and irradiance-dependent than on the RWC. |
---|---|
AbstractList | Barbacenia purpurea is a resurrection species endemic to rock outcrops, in Rio de Janeiro, Brazil. It tolerates great temperature variations, which are associated to periods of up to 30 days without precipitation. Using a metabolomic approach, we analyzed, under winter and summer conditions, changes in the leaf metabolite profile (MP) of potted plants of B. purpurea submitted to daily watered and water deficit for at least 20 days and subsequent slow rehydration for 5 days. Leaves were collected at different time points and had their MP analyzed by GC/MS, HPAEC, and UHPLC techniques, allowing the identification of more than 60 different compounds, including organic and amino acids, sugars, and polyols, among others. In the winter experiment, results suggest the presence of two time-dependent responses in B. purpurea under water stress. The first one starts with the increase in the content of caffeoyl-quinic acids, substances with strong antioxidant activity, until the 16th day of water suppression. When RWC reached less than 80 and 70%, in winter and summer respectively, it was observed an increase in polyols and monosaccharides, followed by an increment in the content of RFO, suggesting osmotic adjustment. Amino acids, such as GABA and asparagine, also increased due to 16 days of water suppression. During rehydration, the levels of the mentioned compounds became similar to those found at the beginning of the experiment and when compared to daily watered plants. We conclude that the tolerance of B. purpurea to dehydration involves the perception of water deficit intensity, which seems to result in different strategies to overcome the gradient of water availability imposed along a certain period of stress mainly during winter. Data from summer experiment indicate that the metabolism of B. pupurea was already primed for drought stress. The accumulation of phenolics in summer seemed to be more temperature and irradiance-dependent than on the RWC.Barbacenia purpurea is a resurrection species endemic to rock outcrops, in Rio de Janeiro, Brazil. It tolerates great temperature variations, which are associated to periods of up to 30 days without precipitation. Using a metabolomic approach, we analyzed, under winter and summer conditions, changes in the leaf metabolite profile (MP) of potted plants of B. purpurea submitted to daily watered and water deficit for at least 20 days and subsequent slow rehydration for 5 days. Leaves were collected at different time points and had their MP analyzed by GC/MS, HPAEC, and UHPLC techniques, allowing the identification of more than 60 different compounds, including organic and amino acids, sugars, and polyols, among others. In the winter experiment, results suggest the presence of two time-dependent responses in B. purpurea under water stress. The first one starts with the increase in the content of caffeoyl-quinic acids, substances with strong antioxidant activity, until the 16th day of water suppression. When RWC reached less than 80 and 70%, in winter and summer respectively, it was observed an increase in polyols and monosaccharides, followed by an increment in the content of RFO, suggesting osmotic adjustment. Amino acids, such as GABA and asparagine, also increased due to 16 days of water suppression. During rehydration, the levels of the mentioned compounds became similar to those found at the beginning of the experiment and when compared to daily watered plants. We conclude that the tolerance of B. purpurea to dehydration involves the perception of water deficit intensity, which seems to result in different strategies to overcome the gradient of water availability imposed along a certain period of stress mainly during winter. Data from summer experiment indicate that the metabolism of B. pupurea was already primed for drought stress. The accumulation of phenolics in summer seemed to be more temperature and irradiance-dependent than on the RWC. Barbacenia purpurea is a resurrection species endemic to rock outcrops, in Rio de Janeiro, Brazil. It tolerates great temperature variations, which are associated to periods of up to 30 days without precipitation. Using a metabolomic approach, we analyzed, under winter and summer conditions, changes in the leaf metabolite profile (MP) of potted plants of B. purpurea submitted to daily watered and water deficit for at least 20 days and subsequent slow rehydration for 5 days. Leaves were collected at different time points and had their MP analyzed by GC/MS, HPAEC, and UHPLC techniques, allowing the identification of more than 60 different compounds, including organic and amino acids, sugars, and polyols, among others. In the winter experiment, results suggest the presence of two time-dependent responses in B. purpurea under water stress. The first one starts with the increase in the content of caffeoyl-quinic acids, substances with strong antioxidant activity, until the 16th day of water suppression. When RWC reached less than 80 and 70%, in winter and summer respectively, it was observed an increase in polyols and monosaccharides, followed by an increment in the content of RFO, suggesting osmotic adjustment. Amino acids, such as GABA and asparagine, also increased due to 16 days of water suppression. During rehydration, the levels of the mentioned compounds became similar to those found at the beginning of the experiment and when compared to daily watered plants. We conclude that the tolerance of B. purpurea to dehydration involves the perception of water deficit intensity, which seems to result in different strategies to overcome the gradient of water availability imposed along a certain period of stress mainly during winter. Data from summer experiment indicate that the metabolism of B. pupurea was already primed for drought stress. The accumulation of phenolics in summer seemed to be more temperature and irradiance-dependent than on the RWC. Barbacenia purpurea is a resurrection species endemic to rock outcrops, in Rio de Janeiro, Brazil. It tolerates great temperature variations, which are associated to periods of up to 30 days without precipitation. Using a metabolomic approach, we analyzed, under winter and summer conditions, changes in the leaf metabolite profile (MP) of potted plants of B. purpurea submitted to daily watered and water deficit for at least 20 days and subsequent slow rehydration for 5 days. Leaves were collected at different time points and had their MP analyzed by GC/MS, HPAEC, and UHPLC techniques, allowing the identification of more than 60 different compounds, including organic and amino acids, sugars, and polyols, among others. In the winter experiment, results suggest the presence of two time-dependent responses in B. purpurea under water stress. The first one starts with the increase in the content of caffeoyl-quinic acids, substances with strong antioxidant activity, until the 16th day of water suppression. When RWC reached less than 80 and 70%, in winter and summer respectively, it was observed an increase in polyols and monosaccharides, followed by an increment in the content of RFO, suggesting osmotic adjustment. Amino acids, such as GABA and asparagine, also increased due to 16 days of water suppression. During rehydration, the levels of the mentioned compounds became similar to those found at the beginning of the experiment and when compared to daily watered plants. We conclude that the tolerance of B. purpurea to dehydration involves the perception of water deficit intensity, which seems to result in different strategies to overcome the gradient of water availability imposed along a certain period of stress mainly during winter. Data from summer experiment indicate that the metabolism of B. pupurea was already primed for drought stress. The accumulation of phenolics in summer seemed to be more temperature and irradiance-dependent than on the RWC. |
Author | Suguiyama, Vanessa F. Meirelles, Sergio T. Silva, Emerson A. Centeno, Danilo C. Braga, Marcia R. |
AuthorAffiliation | 1 Núcleo de Pesquisa em Fisiologia e Bioquímica, Instituto de Botânica São Paulo, Brazil 2 Departamento de Ecologia, Universidade de São Paulo São Paulo, Brazil 3 Centro de Ciências Naturais e Humanas, Universidade Federal do ABC São Bernardo do Campo, Brazil |
AuthorAffiliation_xml | – name: 3 Centro de Ciências Naturais e Humanas, Universidade Federal do ABC São Bernardo do Campo, Brazil – name: 1 Núcleo de Pesquisa em Fisiologia e Bioquímica, Instituto de Botânica São Paulo, Brazil – name: 2 Departamento de Ecologia, Universidade de São Paulo São Paulo, Brazil |
Author_xml | – sequence: 1 givenname: Vanessa F. surname: Suguiyama fullname: Suguiyama, Vanessa F. – sequence: 2 givenname: Emerson A. surname: Silva fullname: Silva, Emerson A. – sequence: 3 givenname: Sergio T. surname: Meirelles fullname: Meirelles, Sergio T. – sequence: 4 givenname: Danilo C. surname: Centeno fullname: Centeno, Danilo C. – sequence: 5 givenname: Marcia R. surname: Braga fullname: Braga, Marcia R. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24672534$$D View this record in MEDLINE/PubMed |
BookMark | eNp1kl9rFDEUxQep2Fr77JvksT7MdjLJZCYvgi1qCwu-qPgW8ufObmo2GZNMi_1Gfkuzu620ghBIyD33d8LNeVkd-OChql7jZkHIwM_GyaVF22C6aJqGs2fVEWaM1pS13w8enQ-rk5Sui6Tpioz3L6rDlrK-7Qg9qn4vQY5oA1mq4GwGNMUwWgcojCivAZ1HeWedlR5FSHOMoLMNHk1O-ozOZVRSg7cSTXMsCyS6DOHHAp1-A-fCnS1VCW9RWofbhPJtQNluoDYwgTdQCAU6BZ8gITNH61fIQLJay52J9KYIdLiBbelV9XyULsHJ_X5cff344cvFZb38_Onq4v2y1rTjuW77DvdmMMoYPrTAFWjeUUOooqNqqaRtJxuFsVGtGgZmBtAEesOacdSGYkaOq6s91wR5LaZoNzL-EkFasbsIcSVkzFY7ED032GDcDd3AKFGGK8VwMw6GMMOw0YX1bs-aZrUBU0aVo3RPoE8r3q7FKtwIwjvC2PYxp_eAGH7OkLLY2KTLbKWHMCeBO4wJ74eWFumbx15_TR7-ugi6vUDHkFKEUWibd5Mu1tYJ3IhtrMQ2VmIbK7GLVek7-6fvAf2_jj_HSdW2 |
CitedBy_id | crossref_primary_10_1007_s13580_019_00214_9 crossref_primary_10_1146_annurev_arplant_071219_105542 crossref_primary_10_3389_fpls_2019_01396 crossref_primary_10_1016_j_flora_2021_151953 crossref_primary_10_3390_molecules25204664 crossref_primary_10_1007_s00018_021_03913_8 crossref_primary_10_3390_ijms22179108 crossref_primary_10_1093_biosci_biv178 crossref_primary_10_3389_fpls_2021_676632 crossref_primary_10_3389_fpls_2024_1344820 crossref_primary_10_1007_s11103_022_01273_w crossref_primary_10_1038_s41598_017_08448_2 crossref_primary_10_1186_s41065_017_0031_7 crossref_primary_10_1080_15592324_2021_2004025 crossref_primary_10_1016_j_envexpbot_2022_105169 crossref_primary_10_1111_nph_19356 crossref_primary_10_1016_j_ygeno_2023_110592 crossref_primary_10_3390_agriculture13061271 crossref_primary_10_1016_j_sajb_2016_03_021 crossref_primary_10_1016_j_phytochem_2018_12_016 crossref_primary_10_2139_ssrn_4170499 crossref_primary_10_1002_ajb2_1588 crossref_primary_10_1016_j_agwat_2016_04_016 crossref_primary_10_1016_j_apsoil_2024_105618 crossref_primary_10_1016_j_plaphy_2020_02_011 crossref_primary_10_1071_FP17066 crossref_primary_10_3390_ijms21218258 crossref_primary_10_3390_horticulturae7060125 crossref_primary_10_1016_j_envexpbot_2017_09_003 crossref_primary_10_1016_j_envexpbot_2018_09_027 crossref_primary_10_1111_pce_13195 crossref_primary_10_1016_j_envexpbot_2024_106007 crossref_primary_10_1016_j_flora_2020_151604 crossref_primary_10_3389_fphys_2015_00206 crossref_primary_10_1016_j_flora_2017_01_001 crossref_primary_10_1111_pbi_13362 crossref_primary_10_3389_fpls_2015_01123 crossref_primary_10_1016_j_scitotenv_2021_145080 crossref_primary_10_1111_1462_2920_13249 crossref_primary_10_1080_23328940_2015_1095270 crossref_primary_10_1002_pca_3351 crossref_primary_10_1093_botlinnean_boab102 crossref_primary_10_1002_ece3_11555 crossref_primary_10_1093_jxb_erab022 crossref_primary_10_1007_s00425_019_03211_5 crossref_primary_10_1142_S0218339021400052 crossref_primary_10_1093_jxb_ery145 crossref_primary_10_1093_jxb_eraa017 crossref_primary_10_4236_ajps_2017_812205 crossref_primary_10_3390_metabo14020113 crossref_primary_10_3389_fpls_2022_853220 crossref_primary_10_3390_metabo13040511 crossref_primary_10_3390_ijms25031492 crossref_primary_10_1016_j_sajb_2020_09_003 crossref_primary_10_1155_2020_4827045 crossref_primary_10_1016_j_indcrop_2024_118129 crossref_primary_10_3389_fpls_2015_00564 crossref_primary_10_1016_j_pbi_2023_102410 crossref_primary_10_1016_j_envexpbot_2021_104397 crossref_primary_10_3389_fpls_2015_00768 crossref_primary_10_1007_s40415_018_0442_3 crossref_primary_10_1007_s11105_020_01238_7 crossref_primary_10_1640_0002_8444_115_1_61 crossref_primary_10_1016_j_plantsci_2021_110994 crossref_primary_10_1016_j_phytochem_2020_112323 crossref_primary_10_3389_fmicb_2018_00010 crossref_primary_10_1111_ppl_12890 crossref_primary_10_1007_s00122_023_04461_4 crossref_primary_10_3390_agronomy11010131 crossref_primary_10_1093_pcp_pcw021 crossref_primary_10_1111_ppl_14035 crossref_primary_10_1111_ppl_13783 |
Cites_doi | 10.1093/jxb/erm056 10.1021/ac60111a017 10.1016/S1360-1385(99)01486-7 10.1016/j.jplph.2011.11.006 10.1023/A:1026534305831 10.1105/tpc.110.082800 10.1016/j.plaphy.2013.07.005 10.1046/j.1365-313x.1991.t01-11-00999.x 10.1079/9781845939953.0238 10.1016/0098-8472(95)00046-1 10.1007/s10886-005-8396-x 10.1111/j.1365-313X.2008.03673.x 10.1023/A:1026565817218 10.1016/j.plantsci.2008.10002 10.1007/s10725-010-9491-8 10.1007/978-94-011-1494-3 10.1093/icb.45.5.696 10.1186/1471-2229-10-20 10.1590/S2236-89062007000400001 10.1007/s00018-012-1155-6 10.1093/jxb/ern297 10.1590/S0100-40422004000400013 10.1007/s11099-013-0063-9 10.1016/B978-0-12-387692-8.00009-6 10.1590/S0100-84042007000400002 10.1093/jxb/erg255 10.1007/s00425-006-0449-z 10.1016/S0031-9422(99)00031-X 10.1017/S0376892999000041 10.1104/pp.112.201400 10.1016/S0021-9258(18)43097-9 10.1016/S0300-9629(96)00272-1 10.1146/annurev.arplant.49.1.281 10.1093/pcp/pcr041 10.1104/pp.112.211391 10.1079/SSR200175 10.1007/s11240-008-9426-5 10.1016/j.jplph.2007.03.004 10.1038/35002501 10.1093/icb/45.5.771 10.1111/j.1744-7348.2006.00104.x 10.1023/A:1005863015130 10.1007/s00018-012-1088-0 10.1111/j.1365-313X.2007.03115.x 10.1016/j.phytochem.2011.02.027 10.1007/s11240-011-9966-y 10.1105/tpc.13.1.11 10.1023/A:1005801610891 10.1071/FP06315 10.1111/j.1469-8137.1950.tb05146.x 10.1111/j.1399-3054.2008.01156.x 10.1016/j.plantsci.2011.01.018 10.1111/j.1365-313X.2010.04312.x |
ContentType | Journal Article |
Copyright | Copyright © 2014 Suguiyama, Silva, Meirelles, Centeno and Braga. 2014 |
Copyright_xml | – notice: Copyright © 2014 Suguiyama, Silva, Meirelles, Centeno and Braga. 2014 |
DBID | AAYXX CITATION NPM 7X8 5PM DOA |
DOI | 10.3389/fpls.2014.00096 |
DatabaseName | CrossRef PubMed MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Directory of Open Access Journals |
DatabaseTitle | CrossRef PubMed MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic PubMed |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Botany |
EISSN | 1664-462X |
ExternalDocumentID | oai_doaj_org_article_79d1d115858643bd9bb610f8d36d61dc PMC3953666 24672534 10_3389_fpls_2014_00096 |
Genre | Journal Article |
GroupedDBID | 5VS 9T4 AAFWJ AAKDD AAYXX ACGFO ACGFS ACXDI ADBBV ADRAZ AENEX AFPKN ALMA_UNASSIGNED_HOLDINGS AOIJS BCNDV CITATION EBD ECGQY GROUPED_DOAJ GX1 HYE IPNFZ KQ8 M48 M~E OK1 PGMZT RIG RNS RPM NPM 7X8 5PM |
ID | FETCH-LOGICAL-c459t-27517d8dbdd982e9bec954d34b4fb24a425a0b11db2b886d8ec3e7d60ffcd4163 |
IEDL.DBID | M48 |
ISSN | 1664-462X |
IngestDate | Wed Aug 27 01:32:04 EDT 2025 Thu Aug 21 18:06:42 EDT 2025 Fri Jul 11 02:54:16 EDT 2025 Thu Apr 03 07:05:26 EDT 2025 Thu Apr 24 22:59:52 EDT 2025 Tue Jul 01 02:44:31 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Keywords | caffeoyl-quinic acids dehydration tolerance raffinose-family oligosaccharides drought metabolomics rock outcrops |
Language | English |
License | This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c459t-27517d8dbdd982e9bec954d34b4fb24a425a0b11db2b886d8ec3e7d60ffcd4163 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 This article was submitted to Plant Physiology, a section of the journal Frontiers in Plant Science. Reviewed by: Miyako Kusano, RIKEN Plant Science Center, Japan; Paul Hills, Stellenbosch University, South Africa Edited by: John Moore, Stellenbosch University, South Africa |
OpenAccessLink | http://journals.scholarsportal.info/openUrl.xqy?doi=10.3389/fpls.2014.00096 |
PMID | 24672534 |
PQID | 1511397824 |
PQPubID | 23479 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_79d1d115858643bd9bb610f8d36d61dc pubmedcentral_primary_oai_pubmedcentral_nih_gov_3953666 proquest_miscellaneous_1511397824 pubmed_primary_24672534 crossref_citationtrail_10_3389_fpls_2014_00096 crossref_primary_10_3389_fpls_2014_00096 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2014-03-14 |
PublicationDateYYYYMMDD | 2014-03-14 |
PublicationDate_xml | – month: 03 year: 2014 text: 2014-03-14 day: 14 |
PublicationDecade | 2010 |
PublicationPlace | Switzerland |
PublicationPlace_xml | – name: Switzerland |
PublicationTitle | Frontiers in plant science |
PublicationTitleAlternate | Front Plant Sci |
PublicationYear | 2014 |
Publisher | Frontiers Media S.A |
Publisher_xml | – name: Frontiers Media S.A |
References | Ayres (B5) 2003 Meirelles (B34) 1997; 6 Bianchi (B7) 1991; 1 Mollo (B36) 2011; 107 Myers (B39) 2000; 403 De Maria (B10) 2004; 27 Nunes-Nesi (B41) 2007; 50 Sherwin (B52) 1998; 24 Velitchkova (B58) 2013; 51 Gómez (B20) 2010; 64 Oliver (B43) 1998; 24 Carvalho (B8) 2013; 71 Farrant (B15) 2012 Roessner (B49) 2001; 13 Garcia (B17) 1997 Morse (B38) 2011 Meirelles (B35) 1999; 26 Gechev (B19) 2012; 69 Jiang (B27) 2007; 225 Gzik (B21) 1996; 36 Albini (B3) 1999; 51 Lea (B29) 2006; 150 Porembski (B46) 2000; 151 Gechev (B18) 2013; 70 Moore (B37) 2005; 31 Cassab (B9) 1998; 49 Hoagland (B23) 1950; 347 Peterbauer (B44) 2001; 11 Akçay (B2) 2012; 169 Klerk (B28) 2008; 95 Toldi (B54) 2009; 176 Renault (B48) 2010; 10 Amaral (B4) 2007; 34 Aidar (B1) 2010; 62 Norwood (B40) 2003; 54 Farrant (B14) 2007; 1 Hoekstra (B24) 1997; 117A Van den Ende (B55) 2009; 60 Somogyi (B53) 1945; 160 Meguro (B33) 1977; 5 Lüttge (B32) 2008; 165 Farrant (B13) 2000; 151 Vertucci (B59) 1995 Renault (B47) 2011; 52 Illing (B25) 2005; 45 Weatherley (B60) 1950; 49 Vandesteene (B56) 2012; 160 Dubois (B12) 1956; 28 Jaiswal (B26) 2011; 72 Lunn (B31) 2007; 34 Dinakar (B11) 2012; 182 Scarano (B50) 2007; 4 Shelp (B51) 1999; 4 Oliver (B42) 2011; 23 Lee (B30) 2008; 143 Farrant (B16) 2009; 57 Peters (B45) 2007; 58 Bartels (B6) 2005; 45 Hendry (B22) 1993 Van Hutte (B57) 2013; 161 |
References_xml | – volume: 58 start-page: 1947 year: 2007 ident: B45 article-title: Protection mechanisms in the resurrection plant Xerophyta viscosa (Baker): both sucrose and raffinose family oligosaccharides (RFOs) accumulate in leaves in response to water deficit publication-title: J. Exp. Bot doi: 10.1093/jxb/erm056 – volume: 28 start-page: 350 year: 1956 ident: B12 article-title: Colorimetric method for determination of sugars and related substances publication-title: Anal. Chem doi: 10.1021/ac60111a017 – volume: 4 start-page: 1360 year: 1999 ident: B51 article-title: Metabolism and functions of gamma-aminobutyric acid publication-title: Trends Plant Sci doi: 10.1016/S1360-1385(99)01486-7 – volume: 169 start-page: 452 year: 2012 ident: B2 article-title: Contribution of gamma amino butyric acid (GABA) to salt stress responses of Nicotiana sylvestris CMSII mutant and wild type plants publication-title: J. Plant Physiol doi: 10.1016/j.jplph.2011.11.006 – volume: 151 start-page: 29 year: 2000 ident: B13 article-title: A comparison of mechanisms of desiccation tolerance among three angiosperm resurrection plant species publication-title: Plant Ecol doi: 10.1023/A:1026534305831 – volume: 23 start-page: 1231 year: 2011 ident: B42 article-title: A sister group contrast using untargeted global metabolic analysis delineates the biochemical regulation underlying desiccation tolerance in Sporobolus stapfianus [C][W][OA] publication-title: Plant Cell doi: 10.1105/tpc.110.082800 – volume: 71 start-page: 144 year: 2013 ident: B8 article-title: Biochemical and anatomical responses related to the in vitro survival of the tropical bromeliad Nidularium minutum to low temperatures publication-title: Plant Physiol. Biochem doi: 10.1016/j.plaphy.2013.07.005 – volume: 1 start-page: 355 year: 1991 ident: B7 article-title: Novel carbohydrate metabolism in the resurrection plant Craterostigma plantagineum publication-title: Plant J doi: 10.1046/j.1365-313x.1991.t01-11-00999.x – start-page: 238 volume-title: Plant Stress Physiology year: 2012 ident: B15 article-title: Desiccation tolerance doi: 10.1079/9781845939953.0238 – volume: 36 start-page: 29 year: 1996 ident: B21 article-title: Accumulation of proline and pattern of α-amino acids in sugar beet plant in response to osmotic, water and salt stress publication-title: Environ. Exp. Bot doi: 10.1016/0098-8472(95)00046-1 – start-page: 237 volume-title: Seed Development and Germination year: 1995 ident: B59 article-title: Acquisition and loss of desiccation tolerance – volume: 1 start-page: 72 year: 2007 ident: B14 article-title: An overview of mechanism of desiccation tolerance in selected angiosperm ressurrection plants publication-title: Plant Stress – volume: 31 start-page: 2823 year: 2005 ident: B37 article-title: The South African and Namibian populations of the resurrection plant Myrothamnus flabellifolius are genetically distinct and display variation in their galloylquinic acid composition publication-title: J. Chem. Ecol doi: 10.1007/s10886-005-8396-x – volume-title: Aspectos fisiológicos de três espécies de Velloziaceae, durante os processos de dessecação de reidratação year: 1997 ident: B17 – volume: 57 start-page: 65 year: 2009 ident: B16 article-title: Desiccation tolerance in the vegetative tissues of the fern Mohria caffrorum is seasonally regulated publication-title: Plant J doi: 10.1111/j.1365-313X.2008.03673.x – volume: 151 start-page: 19 year: 2000 ident: B46 article-title: Granitic and gneissic outcrops (inselbergs) as center os diversity for desiccation-tolerant vascular plants publication-title: Plant Ecol doi: 10.1023/A:1026565817218 – volume: 176 start-page: 187 year: 2009 ident: B54 article-title: Vegetative desiccation tolerance: is a goldmine for bioengineering crops? publication-title: Plant Sci doi: 10.1016/j.plantsci.2008.10002 – volume: 62 start-page: 193 year: 2010 ident: B1 article-title: Desiccation tolerance in Pleurostima purpurea (Velloziaceae) publication-title: Plant Growth Regul doi: 10.1007/s10725-010-9491-8 – start-page: 148 volume-title: Methods in Comparative Plant Ecology year: 1993 ident: B22 article-title: Stress indicators: chlorophylls and carotenoids doi: 10.1007/978-94-011-1494-3 – volume: 45 start-page: 696 year: 2005 ident: B6 article-title: Desiccation tolerance studied in the resurrection plant Craterostigma plantagineum publication-title: Integr. Comp. Biol doi: 10.1093/icb.45.5.696 – volume: 10 start-page: 20 year: 2010 ident: B48 article-title: The Arabidopsis pop2-1 mutant revels the involvement of GABA transaminase in salt stress tolerance publication-title: BMC Plant Biol doi: 10.1186/1471-2229-10-20 – volume: 34 start-page: 425 year: 2007 ident: B4 article-title: Novo método enzimático rápido e sensÃvel de extração e dosagem de amido em materiais vegetais publication-title: Hoehnea doi: 10.1590/S2236-89062007000400001 – volume: 6 start-page: 17 year: 1997 ident: B34 article-title: Potential desiccation tolerant vascular plants from southeastern Brazil publication-title: Pol. J. Environ. Stud – volume: 70 start-page: 689 year: 2013 ident: B18 article-title: Molecular mechanisms of desiccation tolerance in the resurrection glacial relic Haberlea rhodopensis publication-title: Cell. Mol. Life Sci doi: 10.1007/s00018-012-1155-6 – volume: 60 start-page: 9 year: 2009 ident: B55 article-title: Sucrose, sucrosyl oligosaccharides, and oxidative stress: scavenging and salvaging? publication-title: J. Exp. Bot doi: 10.1093/jxb/ern297 – volume: 27 start-page: 586 year: 2004 ident: B10 article-title: Métodos para análise de ácido clorogênico publication-title: QuÃm. Nova doi: 10.1590/S0100-40422004000400013 – volume: 51 start-page: 630 year: 2013 ident: B58 article-title: Effect of high temperature on dehydration-induced alterations in photosynthetic characteristics of the resurrection plant Haberlea rhodopensis publication-title: Photosynthetica doi: 10.1007/s11099-013-0063-9 – start-page: 319 volume-title: Advances in Botanical Research. Plant Responses to Drought and Salinity Stress: Developments in a Post-genomic Era year: 2011 ident: B38 article-title: An overview of the current understanding of desiccation tolerance in the vegetative tissues of higher plants doi: 10.1016/B978-0-12-387692-8.00009-6 – volume: 4 start-page: 561 year: 2007 ident: B50 article-title: Rock outcrop vegetation in Brazil: a brief overview publication-title: Rev. Brasil. Bot doi: 10.1590/S0100-84042007000400002 – volume: 54 start-page: 2313 year: 2003 ident: B40 article-title: Investigation into the ability of roots of the poikilohydric plant Craterostigma plantagineum to survive dehydration stress publication-title: J. Exp. Bot doi: 10.1093/jxb/erg255 – volume: 225 start-page: 1405 year: 2007 ident: B27 article-title: Proteome analysis of leaves from the resurrection plant Boea hygrometrica in response to dehydration and rehydration publication-title: Planta doi: 10.1007/s00425-006-0449-z – volume: 51 start-page: 499 year: 1999 ident: B3 article-title: Galactinol in the leaves of resurrection plant Boea hygroscopica publication-title: Phytochemistry doi: 10.1016/S0031-9422(99)00031-X – volume: 26 start-page: 10 year: 1999 ident: B35 article-title: The vegetation of granite rock outcrops in Rio de Janeiro, Brazil, and the need for its protection publication-title: Environ. Conser doi: 10.1017/S0376892999000041 – volume: 160 start-page: 884 year: 2012 ident: B56 article-title: Expansive evolution of the TREHALOSE-6-PHOSPHATE PHOSPHATASE gene family in Arabidopsis publication-title: Plant Physiol doi: 10.1104/pp.112.201400 – volume: 160 start-page: 61 year: 1945 ident: B53 article-title: A new reagent for the determination of sugars publication-title: J. Biol. Chem doi: 10.1016/S0021-9258(18)43097-9 – volume: 117A start-page: 335 year: 1997 ident: B24 article-title: Membrane stabilization in the dry state publication-title: Comp. Biochem. Phys doi: 10.1016/S0300-9629(96)00272-1 – volume: 49 start-page: 281 year: 1998 ident: B9 article-title: Plant cell wall proteins publication-title: Annu. Rev. Plant Physiol. Plant Mol. Biol doi: 10.1146/annurev.arplant.49.1.281 – volume: 52 start-page: 894 year: 2011 ident: B47 article-title: GABA accumulation causes cell elongation defects and a decrease in expression of genes encoding secreted and cell wall-related proteins in Arabidopsis thaliana publication-title: Plant Cell Physiol doi: 10.1093/pcp/pcr041 – volume: 161 start-page: 1158 year: 2013 ident: B57 article-title: Over-expression of the trehalase gene AtTRE1 leads to increased drought stress tolerance in Arabidopsis and is involved in ABA-induced stomatal closure publication-title: Plant Physiol doi: 10.1104/pp.112.211391 – volume: 11 start-page: 185 year: 2001 ident: B44 article-title: Biochemistry and physiology of raffinose family oligosaccharides and galactosil cyclitois in seeds publication-title: Seed Sci. Res doi: 10.1079/SSR200175 – volume: 95 start-page: 149 year: 2008 ident: B28 article-title: Protection of in vitro grown Arabidopsis seedlings against abiotic stresses publication-title: Plant Cell Tiss. Org. Cult doi: 10.1007/s11240-008-9426-5 – volume: 165 start-page: 172 year: 2008 ident: B32 article-title: Strong quenching of chlorophyll fluorescence in the desiccated state in three poikilohydric and homoiochlorophyllous moss species indicates photo-oxidative protection on highly light-exposed rocks of a tropical inselberg publication-title: J. Plant Physiol doi: 10.1016/j.jplph.2007.03.004 – volume: 403 start-page: 853 year: 2000 ident: B39 article-title: Biodiversity hotspots for conservation priorities publication-title: Nature doi: 10.1038/35002501 – volume: 45 start-page: 771 year: 2005 ident: B25 article-title: The signature of seeds in resurrection plants: a molecular and physiological comparison of desiccation tolerance in seeds and vegetative tissues publication-title: Integr. Comp. Biol doi: 10.1093/icb/45.5.771 – volume: 150 start-page: 1 year: 2006 ident: B29 article-title: Asparagine in plants publication-title: Ann. Appl. Biol doi: 10.1111/j.1744-7348.2006.00104.x – volume: 24 start-page: 193 year: 1998 ident: B43 article-title: “To dryness and beyongâ€â€”preparation for the dried state and rehydration in vegetative desiccation-tolerant plants publication-title: Plant Growth Regul doi: 10.1023/A:1005863015130 – volume: 69 start-page: 3175 year: 2012 ident: B19 article-title: Molecular mechanisms of desiccation tolerance in resurrection plants publication-title: Cell. Mol. Life Sci doi: 10.1007/s00018-012-1088-0 – volume: 347 start-page: 1 year: 1950 ident: B23 article-title: The water culture method for growing plants without soil publication-title: Calif. Agr. Expt. Sta. Circ – volume: 50 start-page: 1093 year: 2007 ident: B41 article-title: Deficiency of mitochondrial fumarase activity in tomato plants impairs photosynthesis via an effect on stomatal function publication-title: Plant J doi: 10.1111/j.1365-313X.2007.03115.x – volume: 72 start-page: 781 year: 2011 ident: B26 article-title: Determination of the hydroxycinnamate profile of 12 members of the Asteraceae family publication-title: Phytochemistry doi: 10.1016/j.phytochem.2011.02.027 – volume: 107 start-page: 141 year: 2011 ident: B36 article-title: Effects of low temperature on growth and non-structural carbohydrates of the imperial bromeliad Alcantarea imperialis cultured in vitro publication-title: Plant Cell Tiss. Org. Cult doi: 10.1007/s11240-011-9966-y – volume: 13 start-page: 131 year: 2001 ident: B49 article-title: Metabolic profiling allows comprehensive phenotyping of genetically and environmentally modified systems publication-title: Plant Cell doi: 10.1105/tpc.13.1.11 – volume: 24 start-page: 203 year: 1998 ident: B52 article-title: Protection mechanisms against excess light in the ressurrection plants Craterostigma wilsii and Xerophyta viscosa publication-title: Plant Growth Regul doi: 10.1023/A:1005801610891 – volume: 34 start-page: 550 year: 2007 ident: B31 article-title: Gene families and evolution of trehalose metabolism in plants publication-title: Funct. Plant Biol doi: 10.1071/FP06315 – volume: 49 start-page: 81 year: 1950 ident: B60 article-title: Studies in the water relations of cotton plant. I. The field measurement of water deficits in leaves publication-title: New Phytol doi: 10.1111/j.1469-8137.1950.tb05146.x – volume: 5 start-page: 27 year: 1977 ident: B33 article-title: Stress hÃdrico e alguns aspectos do comportamento fisiológico de Xerophyta plicata Spreng—Velloziaceae publication-title: Bol. Bot. Univ. São Paulo – volume: 143 start-page: 403 year: 2008 ident: B30 article-title: Water deficit accumulates sugar by starch degradation not by de novo synthesis in white clover leaves (Trifolium repens) publication-title: Physiol. Plant doi: 10.1111/j.1399-3054.2008.01156.x – start-page: 291 volume-title: BioEstat 3.0: aplicações estatÃsticas nas áreas de ciências biológicas e médicas year: 2003 ident: B5 – volume: 182 start-page: 29 year: 2012 ident: B11 article-title: Photosynthesis in desiccation tolerant plants: energy metabolism and antioxidative stress defense publication-title: Plant Sci doi: 10.1016/j.plantsci.2011.01.018 – volume: 64 start-page: 1 year: 2010 ident: B20 article-title: AtTPS1-mediated trehalose 6-phosphate synthesis is essential for embryogenic and vegetative growth and responsiveness to ABA in germinating seeds and stomatal guard cells publication-title: Plant J doi: 10.1111/j.1365-313X.2010.04312.x |
SSID | ssj0000500997 |
Score | 2.3313963 |
SecondaryResourceType | review_article |
Snippet | Barbacenia purpurea is a resurrection species endemic to rock outcrops, in Rio de Janeiro, Brazil. It tolerates great temperature variations, which are... Barbacenia purpurea is a resurrection species endemic to rock outcrops, in Rio de Janeiro, Brazil. It tolerates great temperature variations, which are... |
SourceID | doaj pubmedcentral proquest pubmed crossref |
SourceType | Open Website Open Access Repository Aggregation Database Index Database Enrichment Source |
StartPage | 96 |
SubjectTerms | caffeoyl-quinic acids dehydration tolerance drought Metabolomics Plant Science raffinose-family oligosaccharides Rock outcrops |
SummonAdditionalLinks | – databaseName: DOAJ Directory of Open Access Journals dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9QwELZQxYEL4s3y0iBxKIe069hx7COLqFYIcaKoN8uObXWlJVl1U6r2H_VfMhNnV7sIxIVrnIfjb5z5Jh5_w9g7kUydnFE4xU0qiEEXWlCtF96IxkQZRc7y_armp_LzWXW2U-qLcsKyPHAeuOPaBB6QtuhKo_P0wXiPHj_pIFRQPDT09UWftxNMZVVvoj511vLBKMwcp9WS1Lk5iWVPSaJ_xw0Nav1_opi_Z0ruuJ6TB-z-yBnhQ-7rQ3Ynto_Y3VmHvO76Mbv9El2CH7FHOGlDMYxluKFLgOwOZhfuZkE_MwAja1JjGnYywGqJYwrDckNDCXewwiGnFHWYI-8-gsPvtCxzs8BWF9_D-ry7WkN_1QFVoy82tXN7uikl2cY15B2PECICn38EgmsDUMj9cxA8fMJOTz59-zgvxgIMRSMr0xdlXfE66OBDMLqMBvE2lQxCepl8KR3Odzf1nAdfeq1V0LERsQ5qmlITiOk9ZQdt18bnDDzp3ODxmJAjKm_w3ZSIpfOm5lFUfMKONnjYZlQnpyIZS4tRCgFoCUBLANoBwAk73F6wysIcfz91RgBvTyNF7eEA2pkd7cz-y84m7O3GPCzOQFpWcW3sLtcWORPRaF3KCXuWzWX7qBL9UFkJbKn3DGmvL_st7eJ8UPkWtLCu1Iv_0fmX7B4NB-XOcfmKHfQXl_E1kqnevxnmzS_PcyIq priority: 102 providerName: Directory of Open Access Journals |
Title | Leaf metabolite profile of the Brazilian resurrection plant Barbacenia purpurea Hook. (Velloziaceae) shows two time-dependent responses during desiccation and recovering |
URI | https://www.ncbi.nlm.nih.gov/pubmed/24672534 https://www.proquest.com/docview/1511397824 https://pubmed.ncbi.nlm.nih.gov/PMC3953666 https://doaj.org/article/79d1d115858643bd9bb610f8d36d61dc |
Volume | 5 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9QwELagcOBS8WYLVIPEoRyy1LHj2IcKsYiyQsCJRXuL4timK22T7SaltP-o_5KZJLuwaLlxySHOw_HMZL6xx98w9lIEk4bcKDRxEyJC0JEWVOuFF6IwXnrRZfl-UeOJ_DhNpr_LAfUDWG8N7aie1GQ5H_48u3yDBn9EESf629dhMSfibU482IjIb7Jb6JZSKmfwucf6HdE3oaG0o_fZdt-GZ2oJ_Lehzr-TJ__wRsd32W4PI-FtJ_d77IYv77Pbowqh3uUDdv3J5wFOfYMSpj3G0FfmhioAAj4YLfOrGc1vAAbbRNDUbm6AxRyHGdoViIJy8GCBUqCsdRgjFB_CwTdaqbmaYWvuX0F9Ul3U0FxUQAXqo1U53YYeSnm3voZuEyQ4j7rQzQ1CXjqgKPxHy4H4kE2O3399N476mgxRIRPTRHGa8NRpZ50zOvYGVcAk0glpZbCxzPEXkB9azp2NrdbKaV8Inzp1GELhCPw9YjtlVfonDCxR3-B5HxA2Kmvw25TwcW5Nyr1I-IANV_LIip6wnOpmzDMMXEiAGQkwIwFmrQAH7GB9w6Lj6vj3pSMS8PoyItluT1TL71lvs1lqHHeImHWiEbdZZ6xFsBm0E8op7ooBe7FSjwyNklZa8tJX53WGMIqQtY7lgD3u1GX9qhhdU5wIbEk3FGmjL5st5eykJf4WtNau1N7_6PxTdoeGg9LpuHzGdprluX-O-Kqx--28BB4_TPl-a0O_AO_0K-4 |
linkProvider | Scholars Portal |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Leaf+metabolite+profile+of+the+Brazilian+resurrection+plant+Barbacenia+purpurea+Hook.+%28Velloziaceae%29+shows+two+time-dependent+responses+during+desiccation+and+recovering&rft.jtitle=Frontiers+in+plant+science&rft.au=Vanessa+Fuentes+Suguiyama&rft.au=Emerson+Alves+da+Silva&rft.au=S%C3%A9rgio+Tadeu+Meirelles&rft.au=Danilo+da+Cruz+Centeno&rft.date=2014-03-14&rft.pub=Frontiers+Media+S.A&rft.eissn=1664-462X&rft.volume=5&rft_id=info:doi/10.3389%2Ffpls.2014.00096&rft.externalDBID=DOA&rft.externalDocID=oai_doaj_org_article_79d1d115858643bd9bb610f8d36d61dc |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1664-462X&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1664-462X&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1664-462X&client=summon |