COMPARATIVE THERMAL STABILITY OF PEROXIDASE ISOZYMES FROM TWO FLAX GENOTROPHS

1982 ◽  
Vol 24 (4) ◽  
pp. 427-435 ◽  
Author(s):  
Mary Ann Fieldes ◽  
Hugh Tyson

The thermal stability of peroxidase isozymes was examined in vitro in Linum usitatissimum L. Extracts of main stem tissues of the L and S genotrophs produced by Durrant were heat treated over a range of temperatures and times. Isozymes in treated extracts were separated electrophoretically, and peak areas for the four main anionic isozymes, together with their relative mobilities (Rms), were recorded. Peak areas supplied estimates of relative activities. Short duration treatments at 60° and 70 °C demonstrated differences in thermal stability between isozymes and produced changes in Rm. With prolonged treatment at 40 °C, the thermal stability of one isozyme differed from those of the other three. This isozyme was known to have a higher molecular weight than the others. In addition, prolonged treatment at 40 °C demonstrated increased thermal stability of the three lower molecular weight isozymes of genotroph S compared to those of L.


1980 ◽  
Vol 22 (4) ◽  
pp. 529-534 ◽  
Author(s):  
H. Tyson ◽  
M. A. Fieldes

Anionic peroxidase isozymes from main stem tissues of adult plants of two flax (Linum usitatissimum L.) genotrophs were separated using acrylamide gel electrophoresis. A range of seven acrylamide concentrations was used for the gels, enabling the effect of gel concentration on relative mobility (Rm) to be examined. The regression of log (Rm) on gel concentration was linear for two of the four main isozymes found. Differences in linear regression slope between the L and S flax genotroph isozymes suggested genotroph differences in molecular weight.



2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Gengxin Hao ◽  
Yanyu Hu ◽  
Linfan Shi ◽  
Jun Chen ◽  
Aixiu Cui ◽  
...  

AbstractThe physicochemical properties of chitosan obtained from the shells of swimming crab (Portunus trituberculatus) and prepared via subcritical water pretreatment were examined. At the deacetylation temperature of 90 °C, the yield, ash content, and molecular weight of chitosan in the shells prepared via subcritical water pretreatment were 12.2%, 0.6%, and 1187.2 kDa, respectively. These values were lower than those of shells prepared via sodium hydroxide pretreatment. At the deacetylation temperature of 120 °C, a similar trend was observed in chitosan molecular weight, but differences in chitosan yield and ash content were not remarkable. At the same deacetylation temperature, the structures of chitosan prepared via sodium hydroxide and subcritical water pretreatments were not substantially different. However, the compactness and thermal stability of chitosan prepared via sodium hydroxide pretreatment was lower than those of chitosan prepared via subcritical water pretreatment. Compared with the chitosan prepared by sodium hydroxide pretreatment, the chitosan prepared by subcritical water pretreatment was easier to use in preparing oligosaccharides, including (GlcN)2, via enzymatic hydrolysis with chitosanase. Results suggested that subcritical water pretreatment can be potentially used for the pretreatment of crustacean shells. The residues obtained via this method can be utilized to prepare chitosan.



2020 ◽  
Vol 32 (7) ◽  
pp. 801-822 ◽  
Author(s):  
John J La Scala ◽  
Greg Yandek ◽  
Jason Lamb ◽  
Craig M Paquette ◽  
William S Eck ◽  
...  

4,4′-Methylenedianiline (MDA) is widely used in high-temperature polyimide resins, including polymerization of monomer reactants-15. The toxicity of MDA significantly limits the manufacturability using this resin. Modifying the substitution and electronics of MDA could allow for the reduction of toxicity while maintaining the high-performing properties of the materials derived from the modified MDA. The addition of a single methyl substituent, methoxy substituent, location of these substituents, and location of the amine relative to the phenolic bridge were modified as were other non-aniline diamines. Various anilines were condensed with paraformaldehyde under acidic conditions to yield dianilines. These dianilines and diamines were reacted with nadic anhydride and 3,3′,4,4′-benzophenonetetracarboxylic dianhydride in methanol to form the polyamic acid oligomers and heated at elevated temperature to form polyimide oligomers. It was found that the molecular weight of the oligomers derived from MDA alternatives was generally lower than that of MDA oligomers resulting in lower glass transition temperatures ( T gs) and degradation temperatures. Additionally, methoxy substituents further reduce the T g of the polymers versus methyl substituents and reduce the thermal stability of the resin. Methyl-substituted alternatives produced polyimides with similar T gs and degradation temperatures. The toxicity of the MDA alternatives was examined. Although a few were identified with reduced toxicities, the alternatives with properties similar to that of MDA also had high toxicities.



1991 ◽  
Vol 6 (12) ◽  
pp. 2694-2700 ◽  
Author(s):  
Prashant N. Kumta ◽  
Subhash H. Risbud

GeS2 is known to be a good chalcogenide glass former with a transmission cutoff at 11 μm and has been studied for fiber optic application in the mid infrared region. The rare earth sulfides, oxysulfides, and oxides (La–Er) form reasonably good and stable glasses when mixed with chalcogenides such as Ga2S3. In this work, glass formation was studied in the GeS2−La2S3 system. Two compositions containing 60 mol % and 92.5 mol % GeS2, respectively, were analyzed, and the effects of composition on the microstructure and thermal stability of these glasses were investigated. Microstructural studies were conducted on the as-prepared and heat-treated glasses using TEM and SEM/EDXA. Glasses rich in GeS2 exhibited primary (6–88 nm) and secondary (3–13 nm) phase separation at the molecular level. Differential thermal analysis performed on these glasses indicated glass transition temperatures (Tg) of 510 °C and 420 °C for the two compositions studied. The glasses were stable and the (Tg) was observed to decrease with increasing contents of GeS2 in these glasses.





Author(s):  
Lijie Qu ◽  
Zhenyu Wang ◽  
Jing Qian ◽  
Zhengbin He ◽  
Songlin Yi

Abstract Acidic aluminum sulfate hydrolysis solutions can be used to catalyze the thermal degradation of wood in a mild temperature environment, and thus reduce the temperature required for heat treatment process. To improve the dimensional and thermal stability of Chinese fir during heat treatment at 120 °C, 140 °C and 160 °C, this study investigated the effects of soaking pretreatment with 5%, 10% and 15% aluminum sulfate on the chemical and structural changes of the heat-treated Chinese fir. The results indicated that the samples treated at 15% aluminum sulfate concentration and 160 °C heat treatment achieved the best dimensional and thermal stability. Chemical analyses by Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) indicated that the catalysis of aluminum sulfate resulted in degradation of hemicelluloses during the heat treatment, and an increase in the soaking concentration and heat treatment temperature also affected the thermal degradation of celluloses. The scanning electron microscope (SEM) and mass changes test results proved that the hydrolyzed aluminum flocs mainly adhered to the inner wall of the wood tracheid as spherical precipitates, and when the soaking concentration reached 10% and 15%, a uniform soaking effect could be achieved. The thermogravimetric (TG) analysis revealed the soaking pretreatment effectively improved the thermal stability of the heat-treated wood by physically wrapping and promoting the formation of a carbon layer on the wood surface during heat treatment. Thus, aluminum sulfate soaking pretreatment exerted a great effect on the dimensional and thermal stability of wood, allowing heat treatment to be performed at a lower temperature.





2009 ◽  
Vol 24 (3) ◽  
pp. 235-244 ◽  
Author(s):  
Ryoichi Fujiwara ◽  
Miki Nakajima ◽  
Tetsunori Yamamoto ◽  
Hidemi Nagao ◽  
Tsuyoshi Yokoi


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