scholarly journals Characterizations of Gelatin from the Skin of American Bullfrog (Rana catesbeiana) as Affected by Extraction Temperature

2021 ◽  
Vol 13 (8) ◽  
pp. 4390
Author(s):  
Weibo Zhang ◽  
Chong Chen ◽  
Ziyu Huang ◽  
Pengjie Wang
Keyword(s):  
Rana Catesbeiana ◽  
Industrial Applications ◽  
Extraction Temperature ◽  
Gel Structure ◽  
Melting Temperatures ◽  
American Bullfrog ◽  
Molecular Weight Distributions ◽  
Weight Distributions ◽  
Cross Links ◽  
Lower Temperature

We investigated the effect of extraction temperature on the gel properties of gelatin from the skin of the American bullfrog (Rana catesbeiana) and the mechanisms. The textural and rheological properties of bullfrog gelatin extracted at 45 °C (G45), 55 °C (G55), and 65 °C (G65) were measured. The molecular weight distributions, microstructures, and amino acid compositions of the bullfrog gelatins were also determined. G45, G55, and G65 had gel strengths of 272.1, 225.6, and 205.8 g and hardness values of 28.1, 24.0, and 22.5 N, respectively. The gelling temperatures ranged from 19.3 to 23.9 °C, and the melting temperatures ranged from 28.9 to 31.5 °C. All the results were compared with those of commercial porcine gelatin. We propose that the higher gel strength of G45 with a higher band intensity of α2-chains compared with G55 and G65 was more likely to form ordered and strong cross-links. The gelatin extracted at a lower temperature (G45) had a finer gel structure, suggesting that it would be more difficult to disrupt by applied force. Gelatin extracted at a lower temperature demonstrated better properties with α2-chains and a fine gel structure. These results provide basic information on the extraction of American bullfrog skin gelatin for industrial applications.

Elastically Effective Strand Density in Polymer Networks

1969 ◽  
Vol 42 (5) ◽  
pp. 1285-1293
Author(s):  
N. R. Langley
Keyword(s):  
Molecular Weight ◽  
Statistical Approach ◽  
Main Chain ◽  
Polymer Network ◽  
Polymer Networks ◽  
Entanglement Density ◽  
Molecular Weight Distributions ◽  
Weight Distributions ◽  
Cross Links ◽  
New Criterion

Abstract A new expression is derived which relates the density of elastically effective strands in a polymer network to the densities of random cross-links, main-chain scissions, and entanglements and to the molecular weight distribution of the initial linear polymer. Methods are recommended for characterizing the cross-link and scission densities from measurable sol fractions and for determining the entanglement density empirically. The strand density can be evaluated quite easily for the random and uniform initial molecular weight distributions. The new expression differs appreciably from that of Mullins and Bueche, owing principally to a new criterion for effectively trapping network entanglements. The statistical approach used to derive the strand density is also used in a new derivation of an existing implicit expression for the gel fraction.

scholarly journals Identification and characterization of amphibian SLC26A5 using RNA-Seq

BMC Genomics ◽  
2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Zhongying Wang ◽  
Qixuan Wang ◽  
Hao Wu ◽  
Zhiwu Huang
Keyword(s):  
Amino Acid ◽  
Inner Ear ◽  
Hair Cells ◽  
Rana Catesbeiana ◽  
Site Directed Mutagenesis ◽  
Amino Acid Residues ◽  
Rna Seq ◽  
American Bullfrog ◽  
Frog Species

Abstract Background Prestin (SLC26A5) is responsible for acute sensitivity and frequency selectivity in the vertebrate auditory system. Limited knowledge of prestin is from experiments using site-directed mutagenesis or domain-swapping techniques after the amino acid residues were identified by comparing the sequence of prestin to those of its paralogs and orthologs. Frog prestin is the only representative in amphibian lineage and the studies of it were quite rare with only one species identified. Results Here we report a new coding sequence of SLC26A5 for a frog species, Rana catesbeiana (the American bullfrog). In our study, the SLC26A5 gene of Rana has been mapped, sequenced and cloned successively using RNA-Seq. We measured the nonlinear capacitance (NLC) of prestin both in the hair cells of Rana’s inner ear and HEK293T cells transfected with this new coding gene. HEK293T cells expressing Rana prestin showed electrophysiological features similar to that of hair cells from its inner ear. Comparative studies of zebrafish, chick, Rana and an ancient frog species showed that chick and zebrafish prestin lacked NLC. Ancient frog’s prestin was functionally different from Rana. Conclusions We mapped and sequenced the SLC26A5 of the Rana catesbeiana from its inner ear cDNA using RNA-Seq. The Rana SLC26A5 cDNA was 2292 bp long, encoding a polypeptide of 763 amino acid residues, with 40% identity to mammals. This new coding gene could encode a functionally active protein conferring NLC to both frog HCs and the mammalian cell line. While comparing to its orthologs, the amphibian prestin has been evolutionarily changing its function and becomes more advanced than avian and teleost prestin.

scholarly journals Chemistry of collagen cross-links: glucose-mediated covalent cross-linking of type-IV collagen in lens capsules

1993 ◽  
Vol 296 (2) ◽  
pp. 489-496 ◽  
Author(s):  
A J Bailey ◽  
T J Sims ◽  
N C Avery ◽  
C A Miles
Keyword(s):  
Type Iv Collagen ◽  
Cross Linking ◽  
Mechanical And Thermal Properties ◽  
Maximum Strain ◽  
Scanning Calorimetry ◽  
Melting Temperatures ◽  
Type Iv ◽  
Collagen Molecules ◽  
Cross Links

The incubation of lens capsules with glucose in vitro resulted in changes in the mechanical and thermal properties of type-IV collagen consistent with increased cross-linking. Differential scanning calorimetry (d.s.c.) of fresh lens capsules showed two major peaks at melting temperatures Tm 1 and Tm 2 at approx. 54 degrees C and 90 degrees C, which can be attributed to the denaturation of the triple helix and 7S domains respectively. Glycosylation of lens capsules in vitro for 24 weeks caused an increase in Tm 1 from 54 degrees C to 61 degrees C, while non-glycosylated, control incubated capsules increased to a Tm 1 of 57 degrees C. The higher temperature required to denature the type-IV collagen after incubation in vitro suggested increased intermolecular cross-linking. Glycosylated lens capsules were more brittle than fresh samples, breaking at a maximum strain of 36.8 +/- 1.8% compared with 75.6 +/- 6.3% for the fresh samples. The stress at maximum strain (or ‘strength’) was dramatically reduced from 12.0 to 4.7 N.mm.mg-1 after glycosylation in vitro. The increased constraints within the system leading to loss of strength and increased brittleness suggested not only the presence of more cross-links but a difference in the location of these cross-links compared with the natural lysyl-aldehyde-derived cross-links. The chemical nature of the fluorescent glucose-derived cross-link following glycosylation was determined as pentosidine, at a concentration of 1 pentosidine molecule per 600 collagen molecules after 24 weeks incubation. Pentosidine was also determined in the lens capsules obtained from uncontrolled diabetics at a level of about 1 per 100 collagen molecules. The concentration of these pentosidine cross-links is far too small to account for the observed changes in the thermal and mechanical properties following incubation in vitro, clearly indicating that another as yet undefined, but apparently more important cross-linking mechanism mediated by glucose is taking place.

The Use of Novel F-RAFT Agents in High Temperature and High Pressure Ethene Polymerization: Can Control be Achieved?

2007 ◽  
Vol 60 (10) ◽  
pp. 788 ◽  
Author(s):  
Markus Busch ◽  
Marion Roth ◽  
Martina H. Stenzel ◽  
Thomas P. Davis ◽  
Christopher Barner-Kowollik
Keyword(s):  
Molecular Weight ◽  
High Pressure ◽  
High Temperature ◽  
Degree Of Polymerization ◽  
Molecular Weight Distributions ◽  
High Pressure High Temperature ◽  
Reversible Addition ◽  
Weight Distributions ◽  
Raft Agent ◽  
Initial Results

Simulations are employed to establish the feasibility of achieving controlled/living ethene polymerizations. Such simulations indicate that reversible addition–fragmentation chain transfer (RAFT) agents carrying a fluorine Z group may be suitable to establish control in high-pressure high-temperature ethene polymerizations. Based on these simulations, specific fluorine (F-RAFT) agents have been designed and tested. The initial results are promising and indicate that it may indeed be possible to achieve molecular weight distributions with a polydispersity being significantly lower than that observed in the conventional free radical process. In our initial trials presented here (using the F-RAFT agent isopropylfluorodithioformate), a correlation between the degree of polymerization and conversion can indeed be observed. Both the lowered polydispersity and the linear correlation between molecular weight and conversion indicate that control may in principle be possible.

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