DORMANCY STUDIES IN SEED OF AVENA FATUA: 3. A RELATIONSHIP BETWEEN MALTASE, AMYLASES, AND GIBBERELLIN

1962 ◽  
Vol 40 (12) ◽  
pp. 1659-1673 ◽  
Author(s):  
G. M. Simpson ◽  
J. M. Naylor
Keyword(s):  
Energy Source ◽  
Gibberellic Acid ◽  
Avena Fatua ◽  
Starch Granules ◽  
Raw Starch ◽  
Endosperm Starch ◽  
Hydrolysis Of ◽  
Exogenous Sugar ◽  
Excised Embryos

Initiation of germination in excised embryos requires an exogenous energy source. Normally this is obtained from the endosperm. In dormant seeds the hydrolysis of starch is blocked despite the fact that dormant and non-dormant seeds contain similar amounts of α- and β-amylases. Alone or in combination the amylases are unable to break down raw endosperm starch granules to simple sugars in vitro. Exogenous maltase in combination with α-amylase hydrolyzes raw starch to glucose. Exogenous maltase eliminates the requirement for exogenous sugar. Examination of the maltase content of imbibed dormant and non-dormant seeds showed a marked increase in non-dormant seeds during the first 40 hours. This does not occur in dormant seeds unless they are treated with gibberellic acid. The results lead to the conclusion that an important effect of gibberellic acid is to induce the synthesis of maltase or in some way activate the preformed enzyme.

Effect of 2,4-D on the Hydrolysis of Diclofop-Methyl in Wild Oat (Avena fatua)

Weed Science ◽  
1980 ◽  
Vol 28 (6) ◽  
pp. 725-729 ◽  
Author(s):  
B. D. Hill ◽  
B. G. Todd ◽  
E. H. Stobbe
Keyword(s):  
Enzyme Preparation ◽  
Avena Fatua ◽  
Wild Oat ◽  
Enzymic Hydrolysis ◽  
Standard Assay ◽  
Rate Of Hydrolysis ◽  
Dichlorophenoxy Acetic Acid ◽  
Hydrolysis Of ◽  
Assay Conditions

The basis for 2,4-D [(2,4-dichlorophenoxy)acetic acid] antagonism of diclofop-methyl {methyl 2-[4-(2,4-dichlorophenoxy) phenoxy] propanoate} toxicity to wild oat (Avena fatuaL.) was investigated by studying changes in the metabolism of diclofop-methyl in vitro. An esterase from wild oat, which hydrolyzes diclofop-methyl to the acid diclofop, was extracted, partially purified, and the reaction characterized. The rate of hydrolysis of14C-diclofop-methyl was 0.14 ηmoles/2 h at standard assay conditions of 0.25 mg lyophilized enzyme preparation (19.6% protein) in 0.1 ml phosphate buffer (0.1 M, pH 7.0), substrate 5 μM. The addition of 2,4-D to this reaction did not inhibit14C-diclofop formation. Higher levels of 2,4-D stimulated enzymic hydrolysis.14C-diclofop-methyl was rapidly metabolized to14C-diclofop and polar14C-conjugates when vacuum-infiltrated into wild oat leaf segments. The addition of 2,4-D caused small increases in the rates of both14C-diclofop-methyl de-esterification and14C-diclofop conjugation. It is concluded that 2,4-D does not inhibit the in vitro de-esterification of diclofop-methyl.

Carbohydrate concentrations and interactions in afterripening-responsive dormantAvena fatuacaryopses induced to germinate by gibberellic acid

1993 ◽  
Vol 3 (4) ◽  
pp. 271-278 ◽  
Author(s):  
M. E. Foley ◽  
M. B. Nichols ◽  
S. P. Myers
Keyword(s):  
Gibberellic Acid ◽  
Avena Fatua ◽  
Wild Oat ◽  
Sugar Production ◽  
Carbohydrate Utilization ◽  
Per Se ◽  
Induced Changes ◽  
Over Time ◽  
Excised Embryos

AbstractIt has been proposed that gibberellic acid (GA3) promotes germination by overcoming restrictions in sugar production and utilization in afterripening-responsive dormant caryopses. While their germination rates were similar, germination commenced sooner in afterripened wild oat (Avena fatuaL.) caryopses than in dormant caryopses treated with GA3and dormant excised embryos treated with GA3plus fructose (Fru). Limited germination occurred in dormant excised embryos cultured with GA3alone. Carbohydrate concentrations were measured over time in dormant caryopses and excised embryos whose germination was induced with GA3and GA3plus Fru. The concentration of sucrose (Suc) in the endosperm declined prior to germination of dormant GA3-treated caryopses. Raffinose (Raf) family oligosaccharides in the embryos of dormant GA-treated caryopses remained relatively constant prior to and shortly after the onset of germination. In contrast, Raf family oligosaccharides in the embryos of afterripened caryopses declined prior to germination. Together this suggests Raf family oligosaccharide utilization is not associated with germinationper se.Increased starch levels, which occurred in dormant excised embryos treated with Fru and GA3plus Fru, were associated with dormancy because similar effects were not apparent in afterripened embryos cultured with Fru. An initial decline in the concentration of Raf family oligosaccharides in dormant embryos cultured with GA3or GA3plus Fru seems to be a result of the excision process. GA3appears to stimulate the germination of dormant embryos by enhancing the uptake or utilization of Fru. It appears that GA3and afterripening-induced changes in carbohydrate utilization in dormant caryopses are different.

Bioassay of Gibberellic Acid using Excised Embryos of Avena fatua L.

Nature ◽  
1961 ◽  
Vol 192 (4803) ◽  
pp. 679-680 ◽  
Author(s):  
J. M. NAYLOR ◽  
G. M. SIMPSON
Keyword(s):  
Gibberellic Acid ◽  
Avena Fatua ◽  
Excised Embryos

Increased participation of pentose phosphate pathway in response to afterripening and gibberellic acid treatment in caryopses of Avena fatua

1971 ◽  
Vol 49 (10) ◽  
pp. 1833-1840 ◽  
Author(s):  
J. A. Simmonds ◽  
G. M. Simpson
Keyword(s):  
Oxygen Consumption ◽  
Gibberellic Acid ◽  
Pentose Phosphate Pathway ◽  
Qualitative Change ◽  
Pentose Phosphate ◽  
Avena Fatua ◽  
Starch Degradation ◽  
Phosphogluconate Dehydrogenase ◽  
Key Enzyme ◽  
Excised Embryos

The rates of oxygen consumption of dormant and non-dormant excised embryos of Avena fatua L. before germination are similar. Gibberellic acid (GA) treatment stimulates germination of dormant embryos without affecting oxygen consumption. Thus dormancy is not the result of restricted oxygen uptake. The fat content of dormant and non-dormant caryopses remains constant during germination. Dormant and non-dormant embryos have respiratory quotients near unity supporting the hypothesis that starch degradation occurs before germination. 6-Phosphogluconate dehydrogenase, a key enzyme of the pentose phosphate pathway, is present in dormant and non-dormant dry embryos but the pre-germination C6/C1 ratio of non-dormant embryos is markedly lower than that of dormant embryos, indicating a greater participation of the pentose phosphate pathway in the respiratory metabolism of non-dormant embryos. Release from dormancy is associated with a shift in metabolism from the glycolytic pathway to the pentose phosphate pathway. GA treatment, which stimulates germination of dormant embryos, causes a similar qualitative change in the oxidative metabolism of dormant embryos. Thus the action of GA is to cause the increased degradation of glucose via the pentose phosphate pathway, which is an essential step in the preparation for germination.

High-Pressure Homogenization Alters Physicochemical Properties and In Vitro Digestibility of Chinese Yam (Dioscorea Opposita Thunb.) Starch

2018 ◽  
Vol 18 (1) ◽  
pp. 10-15
Author(s):  
Wang Yi-Wei ◽  
He Yong-Zhao ◽  
An Feng-Ping ◽  
Huang Qun ◽  
Zeng Feng ◽  
...  
Keyword(s):  
High Pressure ◽  
Physicochemical Properties ◽  
Starch Content ◽  
In Vitro Digestibility ◽  
High Pressure Homogenization ◽  
Starch Granules ◽  
Cross Polarization ◽  
Chinese Yam ◽  
Crystal Type

In this study, Chinese yam starch-water suspension (8%) were subjected to high-pressure homogenization (HPH) at 100 MPa for increasing cycle numbers, and its effect of on the physicochemical properties of the starch was investigated. Results of the polarizing microscope observations showed that the starch granules were disrupted (i.e. greater breakdown value) after HPH treatment, followed by a decrease in cross polarization. After three HPH cycles, the crystallinity of starch decreased, while the crystal type remained unaltered. Meanwhile, the contents of rapidly digestible starch and slowly digestible starch were increased. On the contrary, resistant starch content was decreased. Our results indicate that HPH treatment resulted in reduction of starch crystallinity and increase of starch digestibility.

Total Synthesis and Antibacterial Screening of (±)-6,8-Dihydroxy-3- undecyl-3,4-dihydroisochromen-1-one: A Structural Analogue of Metabolites from Ononis natrix

2019 ◽  
Vol 16 (3) ◽  
pp. 245-248
Author(s):  
Hummera Rafique ◽  
Aamer Saeed ◽  
Ehsan Ullah Mughal ◽  
Muhammad Naveed Zafar ◽  
Amara Mumtaz ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Structural Analog ◽  
Diffusion Method ◽  
Bacterial Strains ◽  
Antibacterial Screening ◽  
Maximum Inhibition ◽  
Bacillus Subtilus ◽  
Hydrolysis Of ◽  
Direct Condensation

Background: (±)-6,8-Dihydroxy-3-undecyl-3,4-dihydroisochromen-1-one is one of the structural analog of several substituted undecylisocoumarins isolated from Ononis natrix (Fabaceae), has been successfully synthesized by direct condensation of homopthalic acid (1) with undecanoyl chloride yields isochromen-1-one (2). Methods: Alkaline hydrolysis of (2) gave the corresponding keto-acid (3), which is then reduced to hydroxy acid (4) then its cyclodehydration was carried out with acetic anhydride to afford 3,4- dihydroisochromen-1-one (5). Followed by demethylation step, the synthesis of target 6,8- dihydroxy-7-methyl-3-undecyl-3,4-dihydroisocoumarin (6) was achieved. Results: In vitro antibacterial screening of all the synthesized compounds were carried out against ten bacterial strains by agar well diffusion method. Conclusion: Newly synthesized molecules exhibited moderate antibacterial activity and maximum inhibition was observed against Bacillus subtilus and Salmonella paratyphi.

Studies on the mechanism of acute inhibition of thyroglobulin hydrolysis by iodine

1985 ◽  
Vol 108 (4) ◽  
pp. 511-517 ◽  
Author(s):  
Nandalal Bagchi ◽  
Birdie Shivers ◽  
Thomas R. Brown
Keyword(s):  
Time Course ◽  
Period 2 ◽  
Iodotyrosine Deiodinase ◽  
Rate Of Hydrolysis ◽  
Underlying Mechanisms ◽  
Excess Iodide ◽  
Sites Of Action ◽  
Hydrolysis Of

Abstract. Iodine in excess is known to acutely inhibit thyroidal secretion. In the present study we have characterized the time course of the iodine effect in vitro and investigated the underlying mechanisms. Labelled thyroid glands were cultured in vitro in medium containing mononitrotyrosine, an inhibitor of iodotyrosine deiodinase. The rate of hydrolysis of labelled thyroglobulin was measured as the proportion of labelled iodotyrosines and iodothyronines recovered at the end of culture and was used as an index of thyroidal secretion. Thyrotrophin (TSH) administered in vivo acutely stimulated the rate of thyroglobulin hydrolysis. Addition of Nal to the culture medium acutely inhibited both basal and TSH-stimulated thyroglobulin hydrolysis. The effect of iodide was demonstrable after 2 h, maximal after 6 h and was not reversible upon removal of iodide. Iodide abolished the dibutyryl cAMP induced stimulation of thyroglobulin hydrolysis. Iodide required organic binding of iodine for its effect but new protein or RNA synthesis was not necessary. The inhibitory effects of iodide and lysosomotrophic agents such as NH4C1 and chloroquin on thyroglobulin hydrolysis were additive suggesting different sites of action. Iodide added in vitro altered the distribution of label in prelabelled thyroglobulin in a way that suggested increased coupling in the thyroglobulin molecule. These data indicate that 1) the iodide effect occurs progressively over a 6 h period, 2) continued presence of iodide is not necessary once the inhibition is established, 3) iodide exerts its action primarily at a post cAMP, prelysosomal site and 4) the effect requires organic binding of iodine, but not new RNA or protein synthesis. Our data are consistent with the hypothesis that excess iodide acutely inhibits thyroglobulin hydrolysis by increasing the resistance of thyroglobulin to proteolytic degradation through increased iodination and coupling.

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