Literature DB >> 11554479

Cell wall metabolism in fruit softening and quality and its manipulation in transgenic plants.

D A Brummell1, M H Harpster.   

Abstract

Excessive softening is the main factor limiting fruit shelf life and storage. Transgenic plants modified in the expression of cell wall modifying proteins have been used to investigate the role of particular activities in fruit softening during ripening, and in the manufacture of processed fruit products. Transgenic experiments show that polygalacturonase (PG) activity is largely responsible for pectin depolymerization and solubilization, but that PG-mediated pectin depolymerization requires pectin to be de-methyl-esterified by pectin methylesterase (PME), and that the PG beta-subunit protein plays a role in limiting pectin solubilization. Suppression of PG activity only slightly reduces fruit softening (but extends fruit shelf life), suppression of PME activity does not affect firmness during normal ripening, and suppression of beta-subunit protein accumulation increases softening. All these pectin-modifying proteins affect the integrity of the middle lamella, which controls cell-to-cell adhesion and thus influences fruit texture. Diminished accumulation of either PG or PME activity considerably increases the viscosity of tomato juice or paste, which is correlated with reduced polyuronide depolymerization during processing. In contrast, suppression of beta-galactosidase activity early in ripening significantly reduces fruit softening, suggesting that the removal of pectic galactan side-chains is an important factor in the cell wall changes leading to ripening-related firmness loss. Suppression or overexpression of endo-(1-->4)beta-D-glucanase activity has no detectable effect on fruit softening or the depolymerization of matrix glycans, and neither the substrate nor the function for this enzyme has been determined. The role of xyloglucan endotransglycosylase activity in softening is also obscure, and the activity responsible for xyloglucan depolymerization during ripening, a major contributor to softening, has not yet been identified. However, ripening-related expansin protein abundance is directly correlated with fruit softening and has additional indirect effects on pectin depolymerization, showing that this protein is intimately involved in the softening process. Transgenic work has shown that the cell wall changes leading to fruit softening and textural changes are complex, and involve the coordinated and interdependent activities of a range of cell wall-modifying proteins. It is suggested that the cell wall changes caused early in ripening by the activities of some enzymes, notably beta-galactosidase and ripening-related expansin, may restrict or control the activities of other ripening-related enzymes necessary for the fruit softening process.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11554479

Source DB:  PubMed          Journal:  Plant Mol Biol        ISSN: 0167-4412            Impact factor:   4.076


  128 in total

1.  Nature and regulation of pistil-expressed genes in tomato.

Authors:  S B Milligan; C S Gasser
Journal:  Plant Mol Biol       Date:  1995-07       Impact factor: 4.076

2.  Purification and properties of wall-bound endo-1, 4-beta-glucanase from suspension-cultured poplar cells.

Authors:  Y Ohmiya; T Takeda; S Nakamura; F Sakai; T Hayashi
Journal:  Plant Cell Physiol       Date:  1995-06       Impact factor: 4.927

3.  Cloning, molecular characterization and expression pattern of a strawberry ripening-specific cDNA with sequence homology to pectate lyase from higher plants.

Authors:  N Medina-Escobar; J Cárdenas; E Moyano; J L Caballero; J Muñoz-Blanco
Journal:  Plant Mol Biol       Date:  1997-08       Impact factor: 4.076

4.  Characterisation of two tomato fruit-expressed cDNAs encoding xyloglucan endo-transglycosylase.

Authors:  D A Arrowsmith; J de Silva
Journal:  Plant Mol Biol       Date:  1995-06       Impact factor: 4.076

5.  The tomato Never-ripe locus regulates ethylene-inducible gene expression and is linked to a homolog of the Arabidopsis ETR1 gene.

Authors:  H C Yen; S Lee; S D Tanksley; M B Lanahan; H J Klee; J J Giovannoni
Journal:  Plant Physiol       Date:  1995-04       Impact factor: 8.340

6.  Auxin-regulated genes encoding cell wall-modifying proteins are expressed during early tomato fruit growth.

Authors:  C Catalá; J K Rose; A B Bennett
Journal:  Plant Physiol       Date:  2000-02       Impact factor: 8.340

7.  Xyloglucan endotransglycosylase: evidence for the existence of a relatively stable glycosyl-enzyme intermediate.

Authors:  Z Sulová; M Takácová; N M Steele; S C Fry; V Farkas
Journal:  Biochem J       Date:  1998-03-15       Impact factor: 3.857

8.  Probing expansin action using cellulose/hemicellulose composites.

Authors:  S E Whitney; M J Gidley; S J McQueen-Mason
Journal:  Plant J       Date:  2000-05       Impact factor: 6.417

9.  A family of at least seven beta-galactosidase genes is expressed during tomato fruit development.

Authors:  D L Smith; K C Gross
Journal:  Plant Physiol       Date:  2000-07       Impact factor: 8.340

10.  Reduction of polygalacturonase activity in tomato fruit by antisense RNA.

Authors:  R E Sheehy; M Kramer; W R Hiatt
Journal:  Proc Natl Acad Sci U S A       Date:  1988-12       Impact factor: 11.205

View more
  180 in total

1.  Pectate lyase gene expression and enzyme activity in ripening banana fruit.

Authors:  M C Marín-Rodríguez; D L Smith; K Manning; J Orchard; G B Seymour
Journal:  Plant Mol Biol       Date:  2003-04       Impact factor: 4.076

Review 2.  Genetic regulation of fruit development and ripening.

Authors:  James J Giovannoni
Journal:  Plant Cell       Date:  2004-03-09       Impact factor: 11.277

3.  Cloning, expression and characterization of a metagenome derived thermoactive/thermostable pectinase.

Authors:  Rajvinder Singh; Samriti Dhawan; Kashmir Singh; Jagdeep Kaur
Journal:  Mol Biol Rep       Date:  2012-06-19       Impact factor: 2.316

4.  Protective proteins are differentially expressed in tomato genotypes differing for their tolerance to low-temperature storage.

Authors:  D Page; B Gouble; B Valot; J P Bouchet; C Callot; A Kretzschmar; M Causse; C M C G Renard; M Faurobert
Journal:  Planta       Date:  2010-05-18       Impact factor: 4.116

5.  Suppression of N-glycan processing enzymes by deoxynojirimycin in tomato (Solanum lycopersicum) fruit.

Authors:  Darshan Dorairaj; Bijesh Puthusseri; Nandini P Shetty
Journal:  3 Biotech       Date:  2020-04-28       Impact factor: 2.406

6.  Overexpression of the carbohydrate binding module of strawberry expansin2 in Arabidopsis thaliana modifies plant growth and cell wall metabolism.

Authors:  Cristina F Nardi; Natalia M Villarreal; Franco R Rossi; Santiago Martínez; Gustavo A Martínez; Pedro M Civello
Journal:  Plant Mol Biol       Date:  2015-04-03       Impact factor: 4.076

7.  Structural insights into the target specificity of plant invertase and pectin methylesterase inhibitory proteins.

Authors:  Michael Hothorn; Sebastian Wolf; Patrick Aloy; Steffen Greiner; Klaus Scheffzek
Journal:  Plant Cell       Date:  2004-11-04       Impact factor: 11.277

8.  Coating Satsuma mandarin using grapefruit seed extract-incorporated carnauba wax for its preservation.

Authors:  Mee Yeon Won; Sea Cheol Min
Journal:  Food Sci Biotechnol       Date:  2018-02-09       Impact factor: 2.391

9.  Down-regulation of tomato beta-galactosidase 4 results in decreased fruit softening.

Authors:  David L Smith; Judith A Abbott; Kenneth C Gross
Journal:  Plant Physiol       Date:  2002-08       Impact factor: 8.340

10.  Regulation and function of the pepper pectin methylesterase inhibitor (CaPMEI1) gene promoter in defense and ethylene and methyl jasmonate signaling in plants.

Authors:  Soo Hyun An; Hyong Woo Choi; Jeum Kyu Hong; Byung Kook Hwang
Journal:  Planta       Date:  2009-09-24       Impact factor: 4.116

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.