जर्नल ऑफ बायोकैमिस्ट्री एंड सेल बायोलॉजी

खुला एक्सेस

हमारा समूह 1000 से अधिक वैज्ञानिक सोसायटी के सहयोग से हर साल संयुक्त राज्य अमेरिका, यूरोप और एशिया में 3000+ वैश्विक सम्मेलन श्रृंखला कार्यक्रम आयोजित करता है और 700+ ओपन एक्सेस जर्नल प्रकाशित करता है जिसमें 50000 से अधिक प्रतिष्ठित व्यक्तित्व, प्रतिष्ठित वैज्ञानिक संपादकीय बोर्ड के सदस्यों के रूप में शामिल होते हैं।

ओपन एक्सेस जर्नल्स को अधिक पाठक और उद्धरण मिल रहे हैं
700 जर्नल और 15,000,000 पाठक प्रत्येक जर्नल को 25,000+ पाठक मिल रहे हैं

अमूर्त

Efficient synthesis of L-theanine in recombinant Escherichia coli containing ?-Glutamyltranspeptidase gene from Pseudomonas nitroreducens (PnGGT)

PHUMSOMBAT Putthapong1, CHIHARU Sano1, TAKAO Hibi2, TAKAFUMI Itoh2, JUNJI Hayashi1, YOSUKE Toyotake1,MAMORU Wakayama1

L-Theanine (γ-glutamylethylamide) is a non-protein amino corrosive present in tea. It adds to the umami taste and exceptional flavor to green tea implantation. It was accounted for to have numerous advantageous physiological impact, particularly hostile to stress and improvement of fixation for learning capacity. It very well may be acquired by substance combination or extraction from green tea, however the two procedures include tedious, cost-insufficient and confounded operational procedure. Henceforth, biotechnological creation of L-theanine become fascinating by utilizing microbial compound, for example, glutamyltranspeptidase (GGT). GGT (EC 2.3.2.2), a heterodimeric protein found in different sources
from microorganisms to warm blooded animals catalyzes the exchange of the γ-glutamyl moiety of γ-glutamyl compound to γ-glutamyl acceptors, for example, amino acids and peptides. Bacterial GGTs have been accounted for in Escherichia coli (EcGGT), Bacillus licheniformis (BlGGT), and Pseudomonas nitroreducens (PnGGT). Our past examination on location coordinated mutagenesis of PnGGT proposed that Trp525 was a key amino corrosive buildup in deciding the inclination of acceptor substrate in the response. Besides, E. coli delivering W525D freak of PnGGT (E. coli-W525D freak) indicated low hydrolysis action with high exchange movement, causing the expansion of L-theanine creation from ethylamine and L-glutamine. Improving the proficiency of L-theanine creation utilizing E. coli - W525D freak was additionally accomplished by entire cell calcium-alginate immobilization with assurance of ideal pH, temperature, and molar substrate proportion. Under the appropriate condition, pH 11, 40ºC, and substrate molar proportion of 1:10, L-glutamine: ethylamine, E. coli W525D freak showed the most noteworthy theanine creation contrasted with P. nitroreducens, E. coli-wild sort, and other recombinant freak strains.