Immunofluorescence localization of ?-amylase in the scutellum, germ aleurone and ?normal? aleurone of germinated barley grains

PROTOPLASMA ◽  
1989 ◽  
Vol 151 (2-3) ◽  
pp. 128-136 ◽  
Author(s):  
B. J. Pogson ◽  
A. E. Ashford ◽  
F. Gubler
2007 ◽  
Vol 57 (2) ◽  
pp. 85-89 ◽  
Author(s):  
Makoto Kihara ◽  
Yoshihiro Okada ◽  
Takashi Iimure ◽  
Kazutoshi Ito

Foods ◽  
2020 ◽  
Vol 9 (3) ◽  
pp. 296 ◽  
Author(s):  
Daniel Rico ◽  
Elena Peñas ◽  
María del Carmen García ◽  
Cristina Martínez-Villaluenga ◽  
Dilip K. Rai ◽  
...  

The increasing demand for healthy food products has promoted the use of germinated seeds to produce functional flours. In this study, germination conditions were optimized in barley grains with the aim to produce flours with high nutritional and biofunctional potential using response surface methodology (RSM). The impact of germination time (0.8–6 days) and temperature (12–20 °C) on barley quality was studied. Non-germinated barley was used as the control. The content of vitamins B1, B2 and C, and proteins increased notably after germination, especially at longer times, while levels of fat, carbohydrates, fibre, and β-glucan were reduced. Total phenolic compounds, γ-aminobutyric acid and antioxidant activity determined by Oxygen Radical Absorbance Capacity increased between 2-fold and 4-fold during sprouting, depending on germination conditions and this increase was more pronounced at higher temperatures (16–20 °C) and longer times (5–6 days). Procyanidin B and ferulic acid were the main phenolics in the soluble and insoluble fraction, respectively. Procyanidin B levels decreased while bound ferulic acid content increased during germination. Germinated barley flours exhibited lower brightness and a higher glycemic index than the control ones. This study shows that germination at 16 °C for 3.5 days was the optimum process to obtain nutritious and functional barley flours. Under these conditions, sprouts retained 87% of the initial β-glucan content, and exhibited levels of ascorbic acid, riboflavin, phenolic compounds and GABA between 1.4-fold and 2.5-fold higher than the non-sprouted grain.


2001 ◽  
Vol 120 (5) ◽  
pp. A676-A676
Author(s):  
O KANAUCHI ◽  
K BREWERY ◽  
K MITSUYAMA ◽  
A ANDOH ◽  
Y ARAKI ◽  
...  

2004 ◽  
Vol 15 (3) ◽  
pp. 1146-1159 ◽  
Author(s):  
Susan L. Kline-Smith ◽  
Alexey Khodjakov ◽  
Polla Hergert ◽  
Claire E. Walczak

The complex behavior of chromosomes during mitosis is accomplished by precise binding and highly regulated polymerization dynamics of kinetochore microtubules. Previous studies have implicated Kin Is, unique kinesins that depolymerize microtubules, in regulating chromosome positioning. We have characterized the immunofluorescence localization of centromere-bound MCAK and found that MCAK localized to inner kinetochores during prophase but was predominantly centromeric by metaphase. Interestingly, MCAK accumulated at leading kinetochores during congression but not during segregation. We tested the consequences of MCAK disruption by injecting a centromere dominant-negative protein into prophase cells. Depletion of centromeric MCAK led to reduced centromere stretch, delayed chromosome congression, alignment defects, and severe missegregation of chromosomes. Rates of chromosome movement were unchanged, suggesting that the primary role of MCAK is not to move chromosomes. Furthermore, we found that disruption of MCAK leads to multiple kinetochore–microtubule attachment defects, including merotelic, syntelic, and combined merotelic-syntelic attachments. These findings reveal an essential role for Kin Is in prevention and/or correction of improper kinetochore–microtubule attachments.


2014 ◽  
Vol 131 ◽  
pp. 44-49 ◽  
Author(s):  
Flávia Daiana Montanuci ◽  
Camila Augusto Perussello ◽  
Luiz Mario de Matos Jorge ◽  
Regina Maria Matos Jorge

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