scholarly journals Intraspecies differences in cold hardiness, carbohydrate content and  -amylase gene expression of Vaccinium corymbosum during cold acclimation and deacclimation

2012 ◽  
Vol 32 (12) ◽  
pp. 1533-1540 ◽  
Author(s):  
J. H. Lee ◽  
D. J. Yu ◽  
S. J. Kim ◽  
D. Choi ◽  
H. J. Lee
HortScience ◽  
2008 ◽  
Vol 43 (7) ◽  
pp. 1975-1981 ◽  
Author(s):  
Lisa J. Rowland ◽  
Anik L. Dhanaraj ◽  
Dhananjay Naik ◽  
Nadim Alkharouf ◽  
Ben Matthews ◽  
...  

To gain a better understanding of changes in gene expression associated with cold acclimation in the woody perennial blueberry (Vaccinium corymbosum L.) and ultimately use this information to develop more freeze-tolerant cultivars, a genomics approach based on the analysis of expressed sequence tags (ESTs) and microarrays was undertaken. Initially, two standard cDNA libraries, constructed using RNA from cold-acclimated (CA) and nonacclimated (NA) floral buds of the blueberry cultivar Bluecrop, were used for the generation of ≈2400 ESTs, half from each library. Putative functions were assigned to cDNAs based on homology to other genes/ESTs from GenBank. From contig analyses, 796 and 865 unique transcripts were identified from the CA and NA libraries, respectively. The most highly abundant cDNAs, that were picked many more times from one library than from the other, were identified as representing potentially differentially expressed transcripts. A cDNA microarray was constructed and used to study gene expression under cold-acclimating conditions in the field and cold room. Results indicated that the abundance of transcripts of numerous blueberry genes change during cold acclimation, including genes not found previously to be cold-responsive in Arabidopsis, and, interestingly, more transcripts were found to be upregulated under cold room conditions than under field conditions. Finally, forward and reverse subtracted cDNA libraries were prepared from ‘Bluecrop’ RNA to enrich for transcripts that are expressed at higher levels in floral buds at 400 h and at 0 h of low-temperature exposure, respectively. Many genes encoding putative transcription factors and other proteins related to signal transduction were identified from both libraries.


2017 ◽  
Vol 219 ◽  
pp. 45-52 ◽  
Author(s):  
Duk Jun Yu ◽  
Ju Young Hwang ◽  
Sun Woo Chung ◽  
Hee Duk Oh ◽  
Seok Kyu Yun ◽  
...  

HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 457a-457
Author(s):  
C. L. Haynes ◽  
O. M. Lindstrom ◽  
M. A. Dirr ◽  
R. Severson

Cold hardiness and carbohydrate content of 4 cultivars of field-grown southern magnolia (Magnolia grandiflora L.) were determined monthly during the 1992-1993 winter. Initially, `Claudia Wannamaker', `Little Gem', `Timeless Beauty', and `Victoria' had similar stem and leaf cold hardiness estimates of -6C in October. However, by February `Claudia Wannamaker' and `Victoria' stems were 6 and 3C more cold hardy than `Little Gem' and `Timeless Beauty' stems. `Claudia Wannamaker' leaves were also 6C more cold hardy than `Little Gem' and `Timeless Beauty' leaves in February. Carbohydrate analysis indicates increases in oligosaccharides during cold acclimation in fall.


2004 ◽  
Vol 81 (2) ◽  
pp. 125-135 ◽  
Author(s):  
Sandra E. Vega ◽  
Alfonso H. del Rio ◽  
John B. Bamberg ◽  
Jiwan P. Palta

Author(s):  
H. C. Hurst ◽  
O. Hagenbüchle ◽  
U. Schibler ◽  
P. H. Shaw ◽  
D. L. Cribbs ◽  
...  

2018 ◽  
pp. 57-71
Author(s):  
Rajinder S. Dhindsa ◽  
Antonio Monroy ◽  
Lawrence Wolfraim ◽  
Guangyuan Dong

2010 ◽  
Vol 28 (4) ◽  
pp. 235-239
Author(s):  
Frank P. Henning ◽  
Timothy J. Smalley ◽  
Orville M. Lindstrom ◽  
John M. Ruter

Abstract Plants that maintain their leaves throughout winter may respond differently to fall fertilization than deciduous plants. The effects of fall fertilization on cold hardiness, nutrient uptake, growth and flower production of evergreen versus deciduous azaleas were studied. Rhododendron canescens (Michx.) Sweet and R. × satsuki ‘Wakaebisu’ were grown in containers, outdoors in Athens, GA, under three fall fertigation regimes applied daily as 0.5 liter (0.13 gal) solutions containing: 1) 75 mg·liter−1 N from August 1 through September 29, 2) 75 mg·liter−1 N from August 1 through November 28, and 3) 125 mg·liter−1 N from August 1 through November 28. Stem freeze resistance was analyzed monthly November through March. Growth of azaleas that received 120 days of extended fertigation (August 1 through November 28) was not increased compared to azaleas that received 60 days of extended fertigation (August 1 through September 29). Growth of the two taxa did not differ in their response to fertilization treatments. The high rate of extended fertilization 125 mg·liter−1 N (from August 1 through November 28) reduced stem freeze resistance November through February, while the moderate rate of extended fertilization (75 mg·liter−1 N from August 1 through November 28) reduced azalea freeze resistance in December. Fall fertilization regimes did not produce differences in the timing of cold acclimation, or deacclimation of R. canescens and R. × satsuki. The high rate of extended fertilization promoted early budbreak of R. × satsuki and postponed flower budbreak of R. canescens. Flower production of R. canescens was not affected by fall fertilization, but the high rate of extended fertilization increased flower production of R. × satsuki compared to plants that received the moderate rate of fertilization 75 mg·liter−1 N from August 1 through September 29.


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