1978
DOI: 10.1017/s0043174500032744
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Enzyme Activity in Dormant and Nondormant Large Crabgrass(Digitaria sanguinalis)Seeds Following Hydration

Abstract: In order to germinate successfully, large crabgrass [Digitaria sanguinalis(L.) Scop.] seeds require a period of after-ripening. Some changes, either physical, biochemical or both, must occur in these seeds during this after-ripening process. This paper reports the differences in the activities of several enzymes between dormant (non-after-ripened) and nondormant (after-ripened) large crabgrass seeds at various periods of hydration. The total protein content of dormant seeds does not change during imbibition bu… Show more

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Cited by 11 publications
(11 citation statements)
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“…This enzyme is responsible for initiating the mobilisation of starch in germinating seeds (Fincher, 1989). Similar to our results, Biswas et al (1978) stated that dormant seeds of large crabgrass had very little or no activity of α-amylase, whereas non-dormant seeds showed appreciable activity.…”
supporting
confidence: 90%
See 1 more Smart Citation
“…This enzyme is responsible for initiating the mobilisation of starch in germinating seeds (Fincher, 1989). Similar to our results, Biswas et al (1978) stated that dormant seeds of large crabgrass had very little or no activity of α-amylase, whereas non-dormant seeds showed appreciable activity.…”
supporting
confidence: 90%
“…The homogenate was centrifuged in a refrigerated centrifuge at 4°C for 25 minutes at 10000 rpm. Clean supernatant was decanted and stored at -80°C for enzyme assay (Biswas et al, 1978, with some modifications). α-amylase activity of the seed extract was determined according to the method of Baker (1991) and Bernfeld (1991) with some modifications.…”
mentioning
confidence: 99%
“…Plant amylase was extracted according to Biswas et al (1978) with some modifications. Seeds of B. napus and Brassica oleracea were placed in Petri dishes on moistened paper and were left under germination conditions for 12 h. Subsequently, the germinated seeds were macerated thoroughly in liquid nitrogen using a pestle in a chilled mortar with 10 ml of cold phosphate buffer (0.1 M, pH 7.2).…”
Section: Methodsmentioning
confidence: 99%
“…Enzymes were extracted according to Biswas et al [ 90 ] with slight modifications by Farashah et al [ 91 ]. Three replicates of 0.25 g seeds were ground with LN and suspended in 2.5 mL of chilled 0.1 M phosphate buffer (pH 7.2).…”
Section: Methodsmentioning
confidence: 99%