scholarly journals Studies on the antimicrobial potential and structural characterization of fatty acids extracted from Sydney rock oyster Saccostrea glomerata

Author(s):  
Subbiahanadar Chelladurai Karthikeyan ◽  
Subramanian Velmurugan ◽  
Mariathason Birdilla Selva Donio ◽  
Mariavincent Michaelbabu ◽  
Thavasimuthu Citarasu
2001 ◽  
Vol 74 (3) ◽  
pp. 355-375 ◽  
Author(s):  
Yasuyuki Tanaka

Abstract Structural characterization of naturally occurring polyisoprenes was carried out to solve the mystery of natural rubber (NR), such as the biosynthesis mechanism of rubber formation, the origin of outstanding properties of NR and the role of rubber in rubber trees. The NMR analysis, based on terpenes and polyprenols as models, disclosed the structure of both terminal groups of rubber chain. Structural evidence indicated that the biosynthesis of rubbers from Lactarius mushroom and leaves of high plants starts from trans, trans-farnesyl diphosphate or trans, trans, trans-geranylgeranyl diphosphate and terminates by dephosphorylation to form a hydroxyl terminal group. The biosynthesis of NR was presumed to start from unidentified initiating species containing two trans-isoprene units and peptide group and to terminate forming a phospholipid terminal group. The initiating group of NR associated with proteins formed branch points, which can be decomposed by enzymatic deproteinization. The branch points formed by phospholipid group were decomposed by transesterification with sodium methoxide. Rapid crystallization of NR was explained by the presence of mixed fatty acids synergistically with linked fatty acids, which were included in phospholipid. Saturated fatty acids linked to rubber chain induced crystallization, while mixed unsaturated fatty acids acted as plasticizer and accelerated the crystallization rate. This was confirmed by the preparation of model cis-polyisoprene grafted with stearic acid. The green strength of NR decreased to the same level as synthetic cis-polyisoprene after transesterification, indicating the effect of branching formed by the phospholipid terminal group and fatty acids in NR. The role of NR in Hevea trees was analyzed using NR from Hevea trees never tapped before. The formation of hard gel and oxidative degradation during the storage of NR in Hevea trees suggested that NR acted as a radical scavenger to remove hydroperoxide.


2001 ◽  
Vol 29 (2) ◽  
pp. 107-114 ◽  
Author(s):  
Alberto Ballistreri ◽  
Mario Giuffrida ◽  
Salvatore P.P. Guglielmino ◽  
Santina Carnazza ◽  
Annamaria Ferreri ◽  
...  

2018 ◽  
Vol 108 ◽  
pp. 608-614 ◽  
Author(s):  
Giuseppe Impallomeni ◽  
Alberto Ballistreri ◽  
Giovanni M. Carnemolla ◽  
Maria G. Rizzo ◽  
Marco S. Nicolò ◽  
...  

2007 ◽  
Vol 80 (2) ◽  
pp. 212-230 ◽  
Author(s):  
Jitladda Sakdapipanich ◽  
Kittipong Insom ◽  
Nataphon Phupewkeaw

Abstract It is accepted that NR gives naturally occurring color, which restrict many applications such as light-color products. Therefore, characterization of color substances presenting in NR is very useful to develop the certain methodology to eliminate them completely or partly from NR in the future. In this work, an attempt was made to purify and characterize the color substances extracted from various fractions of Hevea rubber latex by certain methods, using high-resolution structural characterization techniques. It was found that the content of color substances extracted from fresh latex (FL), rubber cream, bottom fraction (BF), Frey Wyssling (FW) particles and STR 20 were different. Based on the high-resolution spectroscopic analyzes, it was found that the color substances extracted from NR were composed of carotenoids, tocotrienol esters, fatty alcohol esters, tocotrienols, unsaturated fatty acids, fatty alcohols, diglyceride and monoglyceride. The results will be useful for rubber-technologist to identify the origin to make obnoxious color in natural rubber, especially in some applications which are restricted by such the color.


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