Characterization of wheat-Secale africanum chromosome 5Ra derivatives carrying Secale specific genes for grain hardness

Planta ◽  
2016 ◽  
Vol 243 (5) ◽  
pp. 1203-1212 ◽  
Author(s):  
Guangrong Li ◽  
Dan Gao ◽  
Shixiao La ◽  
Hongjin Wang ◽  
Jianbo Li ◽  
...  
2017 ◽  
Vol 31 (1) ◽  
pp. 129-138 ◽  
Author(s):  
C. Valderrama-Bravo ◽  
A. Domínguez-Pacheco ◽  
C. Hernández-Aguilar ◽  
R. Zepeda-Bautista ◽  
A. del Real-López ◽  
...  

Abstract In maize plant breeding aimed at producing a hybrid, it is necessary to characterize the parents and hybrids by their agronomic aspects and grain quality so that the processing industry may offer consumers a quality product and also improve its efficiency. This study evaluated the viscoelastic parameters of masa and the chemical and texture properties of tortillas obtained from parent lines (M-54, M55, and CML-242), two single crosses (M54xM55 and M55xM54), and one hybrid (H-70). The morphology of the maize grains and tortillas was analyzed using scanning electron microscopy. The firmness of masa obtained from CML-242 and H-70 maize was higher than that from the other maize genotypes. M-54 tortillas showed the lowest crude fiber content. Otherwise, tortillas obtained from the M55xM54 hard grain had the lowest fat content and extensibility, while H-70 tortillas showed an intermediate breaking point and extensibility. M-54 and M54xM55 tortillas were softer due to their more swollen starch granules. In contrast, rigid tortillas were obtained from CML-242 and H-70. Grain hardness causes different morphology in starch and tortilla of maize genotypes. However, grain hardness did not influence the characteristics of texture in tortillas.


2004 ◽  
Vol 81 (2) ◽  
pp. 287-289 ◽  
Author(s):  
Z. Pan ◽  
W. Song ◽  
F. Meng ◽  
L. Xu ◽  
B. Liu ◽  
...  

Genome ◽  
2012 ◽  
Vol 55 (11) ◽  
pp. 765-774 ◽  
Author(s):  
Meng-Ping Lei ◽  
Guang-Rong Li ◽  
Cheng Liu ◽  
Zu-Jun Yang

Wild Secale species, Secale africanum Stapf., serve as a valuable source for increasing the diversity of cultivated rye (Secale cereale L.) and provide novel genes for wheat improvement. New wheat – S. africanum chromosome 1Rafr addition, 1Rafr(1D) substitution, 1BL.1RafrS and 1DS.1RafrL translocation, and 1RafrL monotelocentric addition lines were identified by chromosome banding and in situ hybridization. Disease resistance screening revealed that chromosome 1RafrS carries resistance gene(s) to new stripe rust races. Twenty-nine molecular markers were localized on S. africanum chromosome 1Rafr by the wheat – S. africanum introgression lines. Twenty markers can also identically amplify other reported wheat – S. cereale chromosome 1R derivative lines, indicating that there is high conservation between the wild and cultivated Secale chromosome 1R. Nine markers displayed polymorphic amplification between S. africanum and S. cereale chromosome 1Rafr derivatives. The comparison of the nucleotide sequences of these polymorphic markers suggested that gene duplication and sequence divergence may have occurred among Secale species during its evolution and domestication.


2009 ◽  
Vol 12 (4) ◽  
pp. 910-928 ◽  
Author(s):  
Imran Pasha ◽  
Faqir Muhammad Anjum ◽  
Masood Sadiq Butt

3 Biotech ◽  
2021 ◽  
Vol 11 (7) ◽  
Author(s):  
Aleksandra Nucia ◽  
Sylwia Okoń ◽  
Marta Tomczyńska-Mleko ◽  
Agnieszka Nawrocka

2015 ◽  
Vol 16 (12) ◽  
pp. 8324-8336 ◽  
Author(s):  
Guangrong Li ◽  
Hongjun Zhang ◽  
Li Zhou ◽  
Dan Gao ◽  
Mengping Lei ◽  
...  

Euphytica ◽  
2019 ◽  
Vol 215 (10) ◽  
Author(s):  
Adoración Cabrera ◽  
Laura Castellano ◽  
Rocío Recio ◽  
Juan B. Alvarez

Author(s):  
B. L. Soloff ◽  
T. A. Rado

Mycobacteriophage R1 was originally isolated from a lysogenic culture of M. butyricum. The virus was propagated on a leucine-requiring derivative of M. smegmatis, 607 leu−, isolated by nitrosoguanidine mutagenesis of typestrain ATCC 607. Growth was accomplished in a minimal medium containing glycerol and glucose as carbon source and enriched by the addition of 80 μg/ ml L-leucine. Bacteria in early logarithmic growth phase were infected with virus at a multiplicity of 5, and incubated with aeration for 8 hours. The partially lysed suspension was diluted 1:10 in growth medium and incubated for a further 8 hours. This permitted stationary phase cells to re-enter logarithmic growth and resulted in complete lysis of the culture.


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