Alleviation of Thermoinhibition in Chickpea Seeds by Putrescine Involves the Ethylene Pathway

1996 ◽  
Vol 23 (4) ◽  
pp. 479 ◽  
Author(s):  
M Gallardo ◽  
I Sanchez-Calle ◽  
PMD Rueda ◽  
AJ Matilla
Keyword(s):  
Molecular Weight ◽  
Carboxylic Acid ◽  
Cicer Arietinum ◽  
Ethylene Production ◽  
Acc Oxidase ◽  
Sharp Decrease ◽  
Acc Synthase ◽  
Cicer Arietinum L ◽  
Adenosyl Methionine ◽  
Stimulation Of

Germination of chickpea (Cicer arietinum L.) was inhibited by supraoptimal temperatures of 30 or 35�C, but the inhibition was alleviated by a relatively low concentration (1 mM) of putrescine (Put). This allevation may be due to (a) stimulation of the 1-aminocyclopropane-1-carboxylate (ACC) synthase and ACC oxidase activities; (b) increased levels of ACC and decreased levels of 1-(malonylamino)cyclopropane-1-carboxylic acid (MACC); or (c) strongly increased ethylene production. Put at 10 mM did not alleviate thermoinhibition, although, as with Put at 1 mM, it did inhibit adenosyl-methionine (AdoMet) decarboxylase. Alleviation conditions resulted in: (a) an induced accumulation of free Put (S) and Put conjugated to substances of low (HS) and high (HP) molecular weight; (b) a decrease in spermidine (Spd) and spermine (Spm) (S and HP); and (c) no alteration in the levels of Spd and Spm (HS) with respect to the absence of Put (1 mM) at 30�C. In the presence of Put (10 mM), increased accumulation of Put (S, HS and HP) was detected, but with a sharp decrease of Spd and Spm (S and HS).

scholarly journals Ethylene Production and 1-Aminocyclopropane-1-Carboxylic Acid Conjugation in Thermoinhibited Cicer arietinum L. Seeds

1991 ◽  
Vol 97 (1) ◽  
pp. 122-127 ◽  
Author(s):  
Mercedes Gallardo ◽  
María del Mar Delgado ◽  
Isabel María Sánchez-Calle ◽  
Angel Jesús Matilla
Keyword(s):  
Carboxylic Acid ◽  
Cicer Arietinum ◽  
Ethylene Production ◽  
Cicer Arietinum L

scholarly journals Expression of Ethylene Biosynthetic Genes in the Gynoecium and Receptacle Associated With Sepal Abscission During Senescence in Delphinium Grandiflorum

2021 ◽  
Author(s):  
Mitsutoshi Okamoto ◽  
Tomoko Niki ◽  
Mirai Azuma ◽  
Kenichi Shibuya ◽  
Kazuo Ichimura
Keyword(s):  
Gene Expression ◽  
Carboxylic Acid ◽  
Ethylene Production ◽  
Acc Oxidase ◽  
Acc Synthase ◽  
Transcript Level ◽  
Flower Senescence ◽  
Biosynthetic Genes ◽  
Transcript Levels ◽  
Highly Sensitive

Abstract Delphinium flowers are highly sensitive to ethylene and its sepals abscise during senescence, which is associated with increases in 1-aminocyclopropane-1-carboxylic acid (ACC) synthase (ACS) and ACC oxidase (ACO) activities and ethylene production in gynoecium and receptacle. Three ACS genes (DgACS1, DgACS2, and DgACS3) and three ACO genes (DgACO1, DgACO2, and DgACO3) were cloned from Delphinium grandiflorum cv. Super Grand Blue. To investigate the contribution of these genes to ethylene production, their expression was analyzed in these genes in the gynoecium and receptacle during natural senescence and following ethylene exposure and pollination. Ethylene production in the gynoecium and receptacle increased during natural flower senescence. The transcript levels of the ACS and ACO genes in these organs, excluding DgACS2 in the receptacle, increased during senescence. Exposure to ethylene accelerated sepal abscission and more strongly increased ethylene production in the receptacle than in the gynoecium. DgACS1 transcript levels in the gynoecium and DgACS2 and DgACO3 transcript levels in the receptacle were increased by ethylene exposure. Pollination accelerated sepal abscission and increased ethylene production in the gynoecium and receptacle. Pollination slightly affected ACS and ACO transcript levels in the gynoecium, whereas DgACO3 transcript level in the receptacle were markedly increased. These results reveal that ACS and ACO gene expression is differently regulated in the gynoecium and receptacle, and some of these genes are more strongly upregulated by ethylene exposure and pollination in the receptacle than in the gynoecium, suggesting the significance of the receptacle to sepal abscission.

scholarly journals Introgression of Sub1 (SUB1) QTL in mega rice cultivars increases ethylene production to the detriment of grain- filling under stagnant flooding

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Sandhya Rani Kuanar ◽  
Kutubuddin Ali Molla ◽  
Krishnendu Chattopadhyay ◽  
Ramani Kumar Sarkar ◽  
Pravat Kumar Mohapatra
Keyword(s):  
Grain Yield ◽  
Ethylene Production ◽  
Stem Elongation ◽  
Starch Synthesis ◽  
Acc Oxidase ◽  
Acc Synthase ◽  
Grain Filling ◽  
Soluble Carbohydrates ◽  
Rice Cultivars ◽  
Oxidase Enzyme

AbstractIn the recent time, Submergence1 (Sub1)QTL, responsible for imparting tolerance to flash flooding, has been introduced in many rice cultivars, but resilience of the QTL to stagnant flooding (SF) is not known. The response of Sub1-introgression has been tested on physiology, molecular biology and yield of two popular rice cultivars (Swarna and Savitri) by comparison of the parental and Sub1-introgression lines (SwarnaSub1 and SavitriSub1) under SF. Compared to control condition SF reduced grain yield and tiller number and increased plant height and Sub1- introgression mostly matched these effects. SF increased ethylene production by over-expression of ACC-synthase and ACC-oxidase enzyme genes of panicle before anthesis in the parental lines. Expression of the genes changed with Sub1-introgression, where some enzyme isoform genes over-expressed after anthesis under SF. Activities of endosperm starch synthesizing enzymes SUS and AGPase declined concomitantly with rise ethylene production in the Sub1-introgressed lines resulting in low starch synthesis and accumulation of soluble carbohydrates in the developing spikelets. In conclusion, Sub1-introgression into the cultivars increased susceptibility to SF. Subjected to SF, the QTL promoted genesis of ethylene in the panicle at anthesis to the detriment of grain yield, while compromising with morphological features like tiller production and stem elongation.

Harvest maturity related changes in the cold-induced activation of 1-aminocyclopropane-1-carboxylic acid metabolism in Granny Smith apples / Efecto del estado de madurez sobre la activación por frío del metabolismo del ácido 1-aminociclopropano-1-carboxílico en manzanas Granny Smith

1999 ◽  
Vol 5 (3) ◽  
pp. 223-228 ◽  
Author(s):  
C. Larrigaudiere ◽  
I. Recasens ◽  
J. Graell ◽  
M. Vendrell
Keyword(s):  
Carboxylic Acid ◽  
Ethylene Production ◽  
Oxidase Activity ◽  
Acid Metabolism ◽  
Cold Treatment ◽  
Acc Oxidase ◽  
Malus Domestica Borkh ◽  
Harvest Dates ◽  
Harmonization Process ◽  
Harvest Maturity

Changes in 1-aminocyclopropane-1-carboxylic acid metabolism in apples ( Malus domestica Borkh cv Granny Smith) were studied in relation to cold storage. Emphasis was given to the differential re sponsiveness of fruits to cold treatment as a function of stage of maturity at harvest. Fruits were held at 1 or 20 °C for 30 days, respectively, or exposed to 1 °C for 10 days and then storaged at 20 °C for up to 30 days. Fruits at 20 °C showed typical climacteric behavior. Differences at 1 °C between maturity stages in ethylene production and ACC oxidase activity were abolished, which showed that cold treatment is an important inducer of climacteric rise in preclimacteric Granny Smith apples. At 1 °C, ethylene production was lower than at 20 °C and the maxima in production were similar for all the stages of maturity, but took place at different times which corresponded exactly to the initial differ ences in harvest dates. After the transfer to 20 °C, fruits exhibited similar behavior as regards ethyl ene production, ACC oxidase activity, and ACC and MACC levels in relation to a harmonization process which is discussed in this study.

Ethylene production and post-pollination development in Dendrobium flowers treated with foreign pollen

2001 ◽  
Vol 28 (5) ◽  
pp. 409 ◽  
Author(s):  
Saichol Ketsa ◽  
Kanokporn Bunya-atichart ◽  
Wouter G. van Doorn
Keyword(s):  
Carboxylic Acid ◽  
Ethylene Production ◽  
Acc Synthase ◽  
Aminooxyacetic Acid ◽  
Foreign Pollen ◽  
Incompatible Pollen ◽  
Ovary Growth

Dendrobium ‘Pompadour’ flowers fade early following pollination. This is associated with increased ethylene production and early epinasty. These effects are also produced by application of 1-aminocyclopropane-1-carboxylic acid (ACC) on the stigma. Pollen (one anther each) from Ruellia tuberosa L. (Acanthaceae) and Caesalpinia pulcherrima (L.) Sw. (Fabaceae) also increased ethylene production and caused early epinasty and fading. Pollen of Hibiscus schizopetalus (Mast.) Hook.f. (Malvaceae), in contrast, had no effect. R. tuberosa pollen increased ACC concentration and ACC synthase activity of the orchid flowers. Aminooxyacetic acid (AOA) pretreatment prior to R. tuberosa pollination prevented early fading, epinasty and the increase in ethylene production. It also prevented the increase in ACC concentration, and ACC synthase activity. Ovary growth was stimulated by Dendrobium ‘Pompadour’ pollinia, not by any of the incompatible pollen. Applied ACC did not promote ovary growth. It is concluded that incompatible pollen can hasten senescence and epinasty by increasing ACC synthase activity and ethylene production. Ovary growth, in contrast, is apparently not primarily regulated by ethylene.

scholarly journals Physiological and Molecular Characterization of the Response to Ethylene during Senescence of Carnation Genotypic Variants

1995 ◽  
Author(s):  
William Woodson ◽  
Shimon Mayak ◽  
Haim Rabinowitch
Keyword(s):  
Ethylene Production ◽  
Dianthus Caryophyllus ◽  
Acc Oxidase ◽  
Acc Synthase ◽  
Early Response ◽  
Vase Life ◽  
Petal Senescence ◽  
Ethylene Treatment ◽  
Novel Proteins ◽  
Exogenous Ethylene

The senescence of carnation (Dianthus caryophyllus L.) flowers is associated with increased production of the phytohormone ethylene, which in turn serves to initiate and regulate the processes involved in programmed petal death. We investigated the regulation of ethylene production and petal senescence in carnation. Several carnation genotypes were identified that exhibited extended vase-life in comparison to flowers from typical commercial cultivars. The capacity of these genotypes to produce ethylene during postharvest vase-life and to respond to exogenous ethylene was investigated. Several genotypes, represented by 'Sandrosa' and 87-37G produced little ethylene durig their postharvest vase-life and as a result failed to exhibit the symptoms (in-rolling and wilting) typical of flowers producing elevated levels of ethylene. These genotypes were further separated by their capacity to respond to exogenous ethylene by both increased ethylene synthesis and premature petal senescence. In one case a genotype (799) was identified that was not capable of responding to exogenous ethylene by either increased ethylene production or premature petal senescence. The regulation of ethylene production during petal senescence was investigated both at the enzyme and gene levels. A full length cDNA was identified for the petal senescence-related ACC synthase gene. Utilizing this, and other ethylene biosynthetic pathway cDNA probes, an increase in both ACC synthase and ACC oxidase mRNAs were detected following ethylene treatment. An increase in ACC oxidase mRNA and enzyme activity was detected within 2-3 h following ethylene treatment, indicating the expression of this gene is an early response to ethylene. An investigation into the expression of novel proteins during petal senescence revealed a number of polypeptides increased in abundance and possibly play a role in the regulation or biochemical processes of senescence. One polypeptide of 70 kDa was identified as being encoded by the previously characterized gene SR12 and possibly represents a b-galactosidase involved in the remobilization of carbohydrates during senescence.

Isolation and characterization of a cDNA encoding an ACC oxidase from Cicer arietinum and its expression during embryogenesis and seed germination

1998 ◽  
Vol 25 (6) ◽  
pp. 765 ◽  
Author(s):  
M.C. Gómez-Jiménez ◽  
A.J. Matilla ◽  
D. Garrido
Keyword(s):  
Molecular Weight ◽  
Cicer Arietinum ◽  
Acc Oxidase ◽  
Protein Product ◽  
Transcriptional Level ◽  
Mrna Levels ◽  
Embryonic Axes ◽  
Chick Pea ◽  
Isolation And Characterization ◽  
Genes Encoding

A full length cDNA (caaco1) encoding a putative ACC-oxidase (ACCO) was isolated and sequenced from embryonic axes of chick-pea (Cicer arietinum L.) seeds, which depend on ethylene synthesis for germination. The deduced protein for caaco1 has a molecular weight of 36 kDa, a high homology with other ACCOs and is apparently found in the cytosolic fraction of the cell. Heterologous expression of this cDNA confirmed that the protein product exhibits ACCO activity and a molecular weight close to 38 kDa. Southern blot analysis shows that there are at least two genes encoding ACCO in the chick-pea genome. The caaco1 mRNA levels in seeds remained constant during the initial stages of embryogenesis decreasing in the latest stages. During germination, caaco1 mRNA levels increase, reaching a maximum at 24 h, coinciding with the maximum percentage of germination (when all seeds are germinated), ACCO activity and ethylene production. It is interesting that there is a shift in the tissue source of the caaco1 mRNA during embryogenesis and germination. While the bulk of the expression was detected in cotyledons during embryogenesis, it was the embryonic axis that provided most of the expression detected during germination. Our data suggest that during embryogenesis ACCO is regulated at the translational level, but during germination at the transcriptional level.

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