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Published online 7 November 2007
Published in Crop Sci 47:2513-2520 (2007)
© 2007 Crop Science Society of America
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Protein Changes during Heat Stress in Three Kentucky Bluegrass Cultivars Differing in Heat Tolerance

Yali Hea and Bingru Huangb,*

a Dep. of Plant Sciences, School of Agriculture and Biology, Shanghai Jiao Tong Univ., Shanghai 201101, P.R. China
b Dep. of Plant Biology and Pathology, Rutgers Univ., New Brunswick, NJ 08901


Figure 1
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Figure 1. Changes in the proportion of yellow leaves in three Kentucky bluegrass cultivars during heat stress. Bars on the top indicate LSD values (p = 0.05) for comparison among cultivars and on the right represent LSD values for comparison between duration of heat stress for a given cultivar.

 

Figure 2
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Figure 2. Changes in total chlorophyll content in leaves of three Kentucky bluegrass cultivars during heat stress. Bars on the top indicate LSD values (p = 0.05) for comparison among cultivars and on the right represent LSD values for comparison between duration of heat stress for a given cultivar.

 

Figure 3
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Figure 3. Changes in cytoplsmic protein content in leaves of three Kentucky bluegrass cultivars during heat stress. Bars on the top indicate LSD values (p = 0.05) for comparison among cultivars and on the right represent LSD values for comparison between duration of heat stress for a given cultivar.

 

Figure 4
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Figure 4. Changes in membrane protein content in leaves of three Kentucky bluegrass cultivars during heat stress. Bars on the top indicate LSD values (p = 0.05) for comparison among cultivars and on the right represent LSD values for comparison between duration of heat stress for a given cultivar.

 

Figure 5
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Figure 5. Protein profiles of cytoplasmic (A) and membrane (B) proteins in leaves of three Kentucky bluegrass cultivars under normal temperature (20°C). Lanes: (1) ‘Midnight’, (2) ‘Eagleton’, (3) ‘Brilliant’; MW, molecular weight; kDa, kiloDalton; Marker-standard protein with known molecular weight.

 

Figure 6
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Figure 6. Protein profiles of cytoplasmic protein in leaves of three Kentucky bluegrass cultivars (A, ‘Brilliant’, B, ‘Eagleton’, and C, ‘Midnight’) during heat stress. Lanes: (1) 20°C for 7 d; (2) 40°C for 7 d; (3) 40°C for 14 d; (4) 40°C for 21 d; (5) 40°C for 28 d; and (6) marker protein. Equal amounts of protein (45 µg) were loaded in each lane. Solid arrows indicate newly induced proteins during heat stress and hollow arrows indicate degraded constitutive proteins during heat stress. MW, molecular weight; kDa, kiloDalton; Marker, standard protein with known molecular weight.

 

Figure 7
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Figure 7. Protein profiles of membrane protein in leaves of three Kentucky bluegrass cultivars (A, ‘Brilliant’; B, ‘Eagleton’; and C, ‘Midnight’) during heat stress. Lanes: (1) 20°C for 7 d; (2) 40 °C for 7 d; (3) 40 °C for 14 d; (4) 40 °C for 21 d; (5) 40 °C for 28 d; and (6) marker protein. Equal amounts of protein (30 µg) were loaded in each lane. Solid Arrows indicate newly induced proteins during heat stress. MW, molecular weight; kDa, kiloDalton; Marker, standard protein with known molecular weight.

 





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