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Restraining Quiescence Release-Related Ageing in Plant Cells: A Case Study in Carrot

The blackening of cut carrots causes substantial economic losses to the food industry. Blackening was not observed in carrots that had been stored underground for less than a year, but the susceptibility to blackening increased with the age of the carrots that were stored underground for longer peri...

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Autores principales: Schulz, Katie, Machaj, Gabriela, Knox, Paul, Hancock, Robert D., Verrall, Susan R., Korpinen, Risto, Saranpää, Pekka, Kärkönen, Anna, Karpinska, Barbara, Foyer, Christine H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605352/
https://www.ncbi.nlm.nih.gov/pubmed/37887309
http://dx.doi.org/10.3390/cells12202465
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author Schulz, Katie
Machaj, Gabriela
Knox, Paul
Hancock, Robert D.
Verrall, Susan R.
Korpinen, Risto
Saranpää, Pekka
Kärkönen, Anna
Karpinska, Barbara
Foyer, Christine H.
author_facet Schulz, Katie
Machaj, Gabriela
Knox, Paul
Hancock, Robert D.
Verrall, Susan R.
Korpinen, Risto
Saranpää, Pekka
Kärkönen, Anna
Karpinska, Barbara
Foyer, Christine H.
author_sort Schulz, Katie
collection PubMed
description The blackening of cut carrots causes substantial economic losses to the food industry. Blackening was not observed in carrots that had been stored underground for less than a year, but the susceptibility to blackening increased with the age of the carrots that were stored underground for longer periods. Samples of black, border, and orange tissues from processed carrot batons and slices, prepared under industry standard conditions, were analyzed to identify the molecular and metabolic mechanisms underpinning processing-induced blackening. The black tissues showed substantial molecular and metabolic rewiring and large changes in the cell wall structure, with a decreased abundance of xyloglucan, pectins (homogalacturonan, rhamnogalacturonan-I, galactan and arabinan), and higher levels of lignin and other phenolic compounds when compared to orange tissues. Metabolite profiling analysis showed that there was a major shift from primary to secondary metabolism in the black tissues, which were depleted in sugars, amino acids, and tricarboxylic acid (TCA) cycle intermediates but were rich in phenolic compounds. These findings suggest that processing triggers a release from quiescence. Transcripts encoding proteins associated with secondary metabolism were less abundant in the black tissues, but there were no increases in transcripts associated with oxidative stress responses, programmed cell death, or senescence. We conclude that restraining quiescence release alters cell wall metabolism and composition, particularly regarding pectin composition, in a manner that increases susceptibility to blackening upon processing.
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spelling pubmed-106053522023-10-28 Restraining Quiescence Release-Related Ageing in Plant Cells: A Case Study in Carrot Schulz, Katie Machaj, Gabriela Knox, Paul Hancock, Robert D. Verrall, Susan R. Korpinen, Risto Saranpää, Pekka Kärkönen, Anna Karpinska, Barbara Foyer, Christine H. Cells Article The blackening of cut carrots causes substantial economic losses to the food industry. Blackening was not observed in carrots that had been stored underground for less than a year, but the susceptibility to blackening increased with the age of the carrots that were stored underground for longer periods. Samples of black, border, and orange tissues from processed carrot batons and slices, prepared under industry standard conditions, were analyzed to identify the molecular and metabolic mechanisms underpinning processing-induced blackening. The black tissues showed substantial molecular and metabolic rewiring and large changes in the cell wall structure, with a decreased abundance of xyloglucan, pectins (homogalacturonan, rhamnogalacturonan-I, galactan and arabinan), and higher levels of lignin and other phenolic compounds when compared to orange tissues. Metabolite profiling analysis showed that there was a major shift from primary to secondary metabolism in the black tissues, which were depleted in sugars, amino acids, and tricarboxylic acid (TCA) cycle intermediates but were rich in phenolic compounds. These findings suggest that processing triggers a release from quiescence. Transcripts encoding proteins associated with secondary metabolism were less abundant in the black tissues, but there were no increases in transcripts associated with oxidative stress responses, programmed cell death, or senescence. We conclude that restraining quiescence release alters cell wall metabolism and composition, particularly regarding pectin composition, in a manner that increases susceptibility to blackening upon processing. MDPI 2023-10-16 /pmc/articles/PMC10605352/ /pubmed/37887309 http://dx.doi.org/10.3390/cells12202465 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Schulz, Katie
Machaj, Gabriela
Knox, Paul
Hancock, Robert D.
Verrall, Susan R.
Korpinen, Risto
Saranpää, Pekka
Kärkönen, Anna
Karpinska, Barbara
Foyer, Christine H.
Restraining Quiescence Release-Related Ageing in Plant Cells: A Case Study in Carrot
title Restraining Quiescence Release-Related Ageing in Plant Cells: A Case Study in Carrot
title_full Restraining Quiescence Release-Related Ageing in Plant Cells: A Case Study in Carrot
title_fullStr Restraining Quiescence Release-Related Ageing in Plant Cells: A Case Study in Carrot
title_full_unstemmed Restraining Quiescence Release-Related Ageing in Plant Cells: A Case Study in Carrot
title_short Restraining Quiescence Release-Related Ageing in Plant Cells: A Case Study in Carrot
title_sort restraining quiescence release-related ageing in plant cells: a case study in carrot
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605352/
https://www.ncbi.nlm.nih.gov/pubmed/37887309
http://dx.doi.org/10.3390/cells12202465
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