Biochemical characterization of phospholipases C from Coffea arabica in response to aluminium stress. (Record no. 52318)
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| fixed length control field | 02438nam a2200229Ia 4500 |
| 003 - CONTROL NUMBER IDENTIFIER | |
| control field | MX-MdCICY |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20250625160224.0 |
| 040 ## - CATALOGING SOURCE | |
| Transcribing agency | CICY |
| 090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN) | |
| Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) | B-18165 |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 250602s9999 xx |||||s2 |||| ||und|d |
| 245 10 - TITLE STATEMENT | |
| Title | Biochemical characterization of phospholipases C from Coffea arabica in response to aluminium stress. |
| 490 0# - SERIES STATEMENT | |
| Volume/sequential designation | Journal of Inorganic BioChemistry, 204, p.110951, 2020 |
| 520 3# - SUMMARY, ETC. | |
| Summary, etc. | Signal transduction in plants determines their successful adaptation to diverse stress factors. Our group employed suspension cells to study the phosphoinositide pathway, which is triggered by aluminium stress. We investigated about members of the PI-specific phospholipase C (PLC)family and evaluated their transcription profiles in Coffea arabica (Ca)suspension cells after 14 days of culture when treated or not with 100 ?M AlCl3. The four CaPLC1-4 members showed changes in their transcript abundance upon AlCl3 treatment. The expression profiles of CaPLC1/2 exhibited a rapid and transitory increase in abundance. In contrast, CaPLC3 and CaPLC4 showed that transcript levels were up-regulated in short times (at 30 s), while only CaPLC4 kept high levels and CaPLC3 was reduced to basal after 3 h of treatment. CaPLC proteins were heterologously expressed, and CaPLC2 and CaPLC4 were tested for in vitro activity in the presence or absence of AlCl3 and compared to Arabidopsis PLC2 (AtPLC2). A crude extract was isolated from coffee cells. CaPLC2 showed a similar inhibition (30 per cent)as in AtPLC2 and in the crude extract, while in CaPLC4, the activity was enhanced by AlCl3. Additionally, we visualized the yellow fluorescent protein PH domain of human PLC?1 (YFP-PHPLC?1)subcellular localization in cells that were treated or not with AlCl3. In non-treated cells, we observed a polar fluorescence signal towards the fused membrane. However, when cells were treated with AlCl3, these signals were disrupted. Finally, this is the first time that PLC activity has been shown to be stimulated in vitro by AlCl3. |
| 650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | PHOSPHOLIPASES C |
| 650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | COFFEA ARABICA |
| 700 12 - ADDED ENTRY--PERSONAL NAME | |
| Personal name | González-Mendoza, V. M. |
| 700 12 - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Sánchez-Sandoval, M. E. |
| 700 12 - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Munnik, T. |
| 700 12 - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Hernández-Sotomayor, S. T. |
| 856 40 - ELECTRONIC LOCATION AND ACCESS | |
| Uniform Resource Identifier | <a href="https://drive.google.com/file/d/1u3Sjt3OoQX_mRyggAjiuQfAUgedQ2q5m/view?usp=drivesdk">https://drive.google.com/file/d/1u3Sjt3OoQX_mRyggAjiuQfAUgedQ2q5m/view?usp=drivesdk</a> |
| Public note | Para ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx |
| 942 ## - ADDED ENTRY ELEMENTS (KOHA) | |
| Source of classification or shelving scheme | Clasificación local |
| Koha item type | Documentos solicitados |
| Lost status | Source of classification or shelving scheme | Damaged status | Not for loan | Collection | Home library | Current library | Shelving location | Date acquired | Total checkouts | Full call number | Date last seen | Price effective from | Koha item type |
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| Clasificación local | Ref1 | CICY | CICY | Documento préstamo interbibliotecario | 25.06.2025 | B-18165 | 25.06.2025 | 25.06.2025 | Documentos solicitados |
