Menu
×
West Ashley Library
Closed (2024 - Christmas)
Phone: (843) 766-6635
Wando Mount Pleasant Library
Closed (2024 - Christmas)
Phone: (843) 805-6888
Village Library
Closed (2024 - Christmas)
Phone: (843) 884-9741
St. Paul's/Hollywood Library
Closed (2024 - Christmas)
Phone: (843) 889-3300
Otranto Road Library
Closed (2024 - Christmas)
Phone: (843) 572-4094
Mt. Pleasant Library
Closed (2024 - Christmas)
Phone: (843) 849-6161
McClellanville Library
Closed (2024 - Christmas)
Phone: (843) 887-3699
Keith Summey North Charleston Library
Closed (2024 - Christmas)
Phone: (843) 744-2489
John's Island Library
Closed (2024 - Christmas)
Phone: (843) 559-1945
Hurd/St. Andrews Library
Closed (2024 - Christmas)
Phone: (843) 766-2546
Folly Beach Library
Closed (2024 - Christmas)
Phone: (843) 588-2001
Edisto Island Library
Closed (2024 - Christmas)
Phone: (843) 869-2355
Dorchester Road Library
Closed (2024 - Christmas)
Phone: (843) 552-6466
John L. Dart Library
Closed (2024 - Christmas)
Phone: (843) 722-7550
Baxter-Patrick James Island
Closed (2024 - Christmas)
Phone: (843) 795-6679
Main Library
Closed (2024 - Christmas)
Phone: (843) 805-6930
Bees Ferry West Ashley Library
Closed (2024 - Christmas)
Phone: (843) 805-6892
Edgar Allan Poe/Sullivan's Island Library
Closed (2024 - Christmas)
Phone: (843) 883-3914
Mobile Library
Closed (2024 - Christmas)
Phone: (843) 805-6909
Today's Hours
West Ashley Library
Closed (2024 - Christmas)
Phone: (843) 766-6635
Wando Mount Pleasant Library
Closed (2024 - Christmas)
Phone: (843) 805-6888
Village Library
Closed (2024 - Christmas)
Phone: (843) 884-9741
St. Paul's/Hollywood Library
Closed (2024 - Christmas)
Phone: (843) 889-3300
Otranto Road Library
Closed (2024 - Christmas)
Phone: (843) 572-4094
Mt. Pleasant Library
Closed (2024 - Christmas)
Phone: (843) 849-6161
McClellanville Library
Closed (2024 - Christmas)
Phone: (843) 887-3699
Keith Summey North Charleston Library
Closed (2024 - Christmas)
Phone: (843) 744-2489
John's Island Library
Closed (2024 - Christmas)
Phone: (843) 559-1945
Hurd/St. Andrews Library
Closed (2024 - Christmas)
Phone: (843) 766-2546
Folly Beach Library
Closed (2024 - Christmas)
Phone: (843) 588-2001
Edisto Island Library
Closed (2024 - Christmas)
Phone: (843) 869-2355
Dorchester Road Library
Closed (2024 - Christmas)
Phone: (843) 552-6466
John L. Dart Library
Closed (2024 - Christmas)
Phone: (843) 722-7550
Baxter-Patrick James Island
Closed (2024 - Christmas)
Phone: (843) 795-6679
Main Library
Closed (2024 - Christmas)
Phone: (843) 805-6930
Bees Ferry West Ashley Library
Closed (2024 - Christmas)
Phone: (843) 805-6892
Edgar Allan Poe/Sullivan's Island Library
Closed (2024 - Christmas)
Phone: (843) 883-3914
Mobile Library
Closed (2024 - Christmas)
Phone: (843) 805-6909
Patron Login
menu
Item request has been placed!
×
Item request cannot be made.
×
Processing Request
Cytosolic fructose-1,6-bisphosphatase isoform mediates metabolic adjustments in bean fruit pericarp to support seed growth.
Item request has been placed!
×
Item request cannot be made.
×
Processing Request
- Author(s): Bernal L;Bernal L; Coello P; Coello P; Padilla-Chacón D; Padilla-Chacón D; Martínez-Barajas E; Martínez-Barajas E
- Source:
Physiologia plantarum [Physiol Plant] 2024 Nov-Dec; Vol. 176 (6), pp. e14631.- Publication Type:
Journal Article- Language:
English - Source:
- Additional Information
- Source: Publisher: Scandinavian Society For Plant Physiology Country of Publication: Denmark NLM ID: 1256322 Publication Model: Print Cited Medium: Internet ISSN: 1399-3054 (Electronic) Linking ISSN: 00319317 NLM ISO Abbreviation: Physiol Plant Subsets: MEDLINE
- Publication Information: Publication: Copenhagen : Scandinavian Society For Plant Physiology
Original Publication: Lund, Sweden [etc.] - Subject Terms: Seeds*/growth & development ; Seeds*/metabolism ; Seeds*/genetics ; Fruit*/growth & development ; Fruit*/metabolism ; Fruit*/genetics ; Fructose-Bisphosphatase*/metabolism ; Fructose-Bisphosphatase*/genetics ; Starch*/metabolism; Photosynthesis/physiology ; Plant Proteins/metabolism ; Plant Proteins/genetics ; Cytosol/metabolism ; Sucrose/metabolism ; Phaseolus/metabolism ; Phaseolus/growth & development ; Phaseolus/genetics ; Phaseolus/enzymology
- Abstract: Seed development requires substantial metabolic resources and is influenced by adverse environmental conditions. However, the ability of plants to produce viable seeds under restrictive conditions suggests the existence of mechanisms that make this process less sensitive to environmental stress. Uncovering their regulation could lead to the development of genotypes better adapted to stressful conditions. Plant response to stress is complex, and the contribution of organs such as the fruit pericarp to stress tolerance mechanism may have been underestimated. The bean fruit pericarp, a photosynthetic structure that contributes to seed development, can synthesize starch from surplus sucrose, which is later degraded during the rapid seed growth phase. This metabolic flexibility may be crucial for supporting seed growth when the photosynthate supply is reduced. To explore this possibility, we disrupted phloem continuity at the pedicel level in fruits about to enter the seed reserve accumulation stage. We used the capacity of the pericarp to incorporate 14 CO
2 to investigate changes in its metabolism. Our findings reveal that, in response to reduced photosynthate availability, the fruit pericarp did not increase 14 CO2 fixation. However, the amount of 14 C used for starch synthesis decreased, while the proportion used for soluble sugars synthesis increased. This shift resulted in an increase in 14 C-products transported to seeds was accompanied by a significant increase in the activity of cytosolic fructose 1,6-bisphosphatase. Our results indicate that photosynthate restriction accelerates the degradation of pericarp storage proteins, and the increase in cFBPase activity could be crucial in converting the carbon produced in carbohydrates.
(© 2024 Scandinavian Plant Physiology Society.) - References: Atkins GA, Kuo J, Pate JS, Flinn AM, Steele TW (1977) Photosynthetic pod wall of pea (Pissum sativum L.): Distribution of carbon dioxide‐fixing enzymes in relation to pod structure. Plant Physiol. 60: 779–786. doi:https://doi.org/10.1104/pp.60.5.779.
Belmont R, Bernal L, Padilla‐Chacón D, Coello P, Martínez‐Barajas E (2022) Starch accumulation in bean fruit pericarp is mediated by the differentiation of chloroplasts into amyloplasts. Plant Sci. 316:111163. doi:https://doi.org/10.1016/j.plantsci.2021.111163.
Bennett E, Roberts JA, Wagstaff C (2011) The role of the pod in seed development. Strategies for manipulating yield. New Phytol. 190:838–853. doi:https://doi.org/10.1111/j.1469-8137.2011.03714.x.
Bernal L, Coello P, Martínez‐Barajas E (2005) Possible role played by R1 protein in starch accumulation in bean (Phaseolus vulgaris) seedlings under phosphate deficiency. Journal of Plant Physiol. 162: 970–976. doi:https://doi.org/10.1016/j.jplph.2004.12.005.
Bernal L, Luján‐Soto E, Fajardo‐Hernández CA, Coello P, Figueroa M, Martínez‐Barajas E (2022) Starch degradation in the bean fruit pericarp is characterized by an increase in maltose metabolism. Physiol Plant. 174:e13836. doi:https://doi.org/10.1111/ppl.13836.
Bravo JA, Fehr W, de Cianzio SR (1980) Use of pod with for indirect selection of seed weigth in soybeans. Crop Sci. 20:507–510. doi:https://doi.org/10.2135/cropsci1980.0011183X002000040022x.
Cho Y‐H, Yoo S‐D (2011) Signaling role of fructose mediated by FINS1/FBP in Arabidopsis thaliana. PLoS Genet. 7(1):e1001263. doi:https://doi.org/10.1371/journal-pgen.1001263. PMID:21256566; PMCID: PMC3017112.
Cho YB, Stutz SS, Jones SI, Wang Y, Palech EA, Ort DR (2023) Impact of pod and seed photosynthesis on seed filling and canopy carbon gain in soybean. Plant Physiol. 193: 966–979. doi:https://doi.org/10.1093/plphys/kiad324.
Clavijo Michelangeli JA, Bhakta M, Gezan SA, Boote KJ, Vallejos CE (2013) From flower to seed: identifying phenological markers and reliable growth functions to model reproductive development in the common bean (Phaseolus vulgaris L.). Plant Cell Environ. 36: 2046–2058. doi:https://doi.org/10.1111/pce.12114.
Garrido A, Conde A, Serôdio J, De Vos RCH, Cunha A (2023) Fruit photosynthesis: more to know about where, how and why. Plants 12:2393. https://doi.org/10.3390/plants12132393.
Huber JL, Huber SC, Nielsen TM (1989) Protein phosphorylation as a mechanism for regulation of spinach leaf sucrose‐phosphate synthase activity. Arch Biochem Biophys. 270: 681–690. doi:https://doi.org/10.1016/0003-9861(89)90551-1.
Laemmli UK (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 227(5259):680–685. doi:https://doi.org/10.1038/227680a0.
Lee S‐K, Jeon J‐S, Börnke F, Voll L, Cho J‐G, Goh C‐H, Jeong S‐K, Park Y‐I, Kim SJ, Choi S‐B, Miyao A, Hirochika H, An G, Cho M‐H, Bhoo SH, Sonnewald U, Hahn T‐R (2008) Loss of cytosolic fructose‐1,6‐bisphosphatase limits photosynthetic sucrose synthesis and causes severe growth retardations in rice (Oryza sativa). Plant Cell Environ. 31: 1851–1863 doi:https://doi.org/10.1111/j.1365-3040.2008.01890.x.
Lee SW, Hahn TR (2003) Light‐regulated differential expression of pea chloroplast and cytosolic fructose‐1,6‐bisphosphatases. Plant Cell Rep. 21(6):611–618. doi:https://doi.org/10.1007/s00299-002-0563-8.
Li C, Wang Y, Huang X, Wang H, Li J (2015) An improved fruit transcriptome and the identification of the candidate genes involved in fruit abscission induced by carbohydrate stress in litchi. Front. Plant Sci. 6:439; doi:https://doi.org/10.3389/fpls.2015.00439.
Li N, Song D, Peng W, Zhan J, Shi J, Wang X, Liu G, Wang H (2019) Maternal control of seed weight in rapeseed (Brassica napus L.): the causal link between the size of pod (mother source) and seed (offspring, sink). Plant Biotech J. 17:736–749. doi:https://doi.org/10.1111/pbi.13011.
Li Y, Sun W, Yao Y, Zhang L, Xu S, Zhang Q, Huang T (2023) FRUCTOSE INSENSITIVE1 regulates stem cell function in Arabidopsis in response to fructose signalling. J Exp Bot. 74:3060–3073. doi:https://doi.org/10.1093/jxb/erad067.
Ma M, Zhu T, Cheng X, Li M, Yuan G, Li G, Zhang A, Lu C, Fang Y, Zhang Y (2024) Sucrose phosphate synthase 8 is required for the remobilization of carbon reserves in rice stems during grain filling. J Exp Bot 75:137–151. doi:https://doi.org/10.1093/jxb/erad375.
Martínez‐Barradas V, Bernal L, López‐Baltazar J, Coello P, Cruz‐García F, Márquez J, Martínez‐Barajas E (2019) Nutritional restriction triggers callose accumulation on the sieve plates of the funiculus of developing seeds. South African J. Bot. 121:549–557 doi:https://doi.org/10.1016/j.sajb.2019.01.024.
Pilkington SM, Encke B, Krohn N, Höhne M, Stitt M, Pyl ET (2015) Relationship between starch degradation and carbon demand for maintenance and growth in Arabidopsis thaliana in different irradiance and temperature regimes. Pant Cell Environ. 38:157–171 doi:https://doi.org/10.1111/pce.12381.
Rao X, Huang X, Zhou Z, Lin X (2013) An improvement of the 2^(−delta delta CT) method for quantitative real time polymerase chain reaction data analysis. Biostat Bioinforma Biomath. 3:71–85.
Rojas‐González JA, Soto‐Suárez M, García‐Díaz A, Romero‐Puertas MC, Sandalio LM, Mérida A, Thormählen I, Geigenberger P, Serrato AJ, Sahrawy M (2015). Disruption of both chloroplastic and cytosolic FBPase genes results in a dwarf phenotype and important starch and metabolite changes in Arabidopsis thaliana. J. Exp. Bot. 66: 2673–2689. doi:https://doi.org/10.1093/jxb/erv062.
Rufty TW, Huber SC (1983) Changes in starch formation and activities of sucrose phosphate synthase and cytoplasmic fructose‐1,6‐bisphosphatase in response to source‐sink alterations. Plant Physiol. 72: 474–480. doi:https://doi.org/10.1104/pp.72.2.474.
Serrato AJ, Yubero‐Serrano EM, Sandalio LM, Muñoz‐Blanco J, Chueca A, Caballero JL, Sahrawy M (2009) cpFBPaseII, a novel redox‐independent chloroplastic isoform of fructose‐1,6‐bisphosphatase. Plant Cell Environ. 32:811–827. doi: https://doi.org/10.1111/j.1365-3040.2009.01960.x.
Simkin AJ, Faralli M, Ramamoorthy S, Lawson T (2020) Photosynthesis in non‐foliar tissues: implications for yield. Plant J. 101:1001–1015. doi:https://doi.org/10.1111/tpj.14633.
Strand A, Zrenner R, Trevanion S, Stitt M, Gustafson P, Gardeström P (2000) Decreased expression of two key enzymes in the sucrose biosynthesis pathway, cytosolic fructose‐1,6‐bisphosphatase and sucrose phosphate synthase, has remarkably different consequences for carbon metabolism in transgenic Arabidopsis thaliana. Plant J. 23 (6): 759–770. doi:https://doi.org/10.1046/j.1365-313x.2000.00847.x.
Toroser D, McMichael R, Krause K‐P, Kurreck J, Sonnewald U, Stitt M, Huber SC (1999) Site‐directed mutagenesis of serine 158 demonstrates its role in spinach leaf sucrose‐phosphate synthase modulation. Plant J. 17: 407–413. doi:https://doi.org/10.1046/j.1365-313x.1999.00389.x.
Untergasser A, Nijveen H, Rao X, Bisseling T, GeurtsR, Leunissen JA (2007) Primer3Plus, an enhanced web interface to Primer3. Nucleic Acid Research 35: W71‐W74. Available from: https://doi.org/10.1093/nar/gkm306.
Wagstaff C, Yang TF, Stead AD, Buchanan‐Wollaton V, Roberts JA (2009) A molecular and structural characterization of senescing Arabidopsis siliques and comparison of transcriptional profiles with senescing petals and leaves. Plant J. 57: 690–705. doi:https://doi.org/10.1111/j.1365-313X.2008.03722.x.
Wang H, Zhou Q, Mao P (2020a) Ultrastructural and photosynthetic responses of pod walls in alfalfa to drought stress. Int. J. Mol. Sci. 21, 4457; doi:https://doi.org/10.3390/ijms21124457.
Wang S, Liu S, Wang J, Yokosho K, Zhou B, Yu Y‐C, Liu Z, Frommer WB, Ma JF, Chen L.Q, Guan Y, Shou H, Tian Z (2020b). Simultaneous changes in seed size, oil content and protein content driven by selection of SWEET homologues during soybean domestication. Natl Sci Rev. 7:1776–1786. doi:https://doi.org/10.1093/nsr/nwaa110.
Wang S, Cao L, Willick IR, Wang H, Tanino KK (2022) Arabidopsis ubiquitin‐conjugating enzymes UBC4, UBC5, and UBC6 have major functions in sugar metabolism and leaf senescence. Int. J. Mol. Sci. 23:11143. https://doi.org/10.3390/ijms231911143.
Zhong P‐Y, Tanaka T, Yamauchi D, Minamikawa T (1997) A 28‐kilodalton pod storage protein of French bean plants. Purification, characterization, and primary structure. Plant Physiol. 113. 479‐485. doi:https://doi.org/10.1104/pp.113.2.479. - Grant Information: IN 205323 Dirección General de Asuntos del Personal Académico, Universidad Nacional Autónoma de México; PAIP 5000-9127 Facultad de Química, UNAM
- Accession Number: EC 3.1.3.11 (Fructose-Bisphosphatase)
9005-25-8 (Starch)
0 (Plant Proteins)
57-50-1 (Sucrose) - Publication Date: Date Created: 20241119 Date Completed: 20241119 Latest Revision: 20241119
- Publication Date: 20241120
- Accession Number: 10.1111/ppl.14631
- Accession Number: 39559930
- Source:
Contact CCPL
Copyright 2022 Charleston County Public Library Powered By EBSCO Stacks 3.3.0 [350.3] | Staff Login
No Comments.