نتایج جستجو برای: phenylalanine ammonialyase

تعداد نتایج: 15360  

Journal: :Catalysts 2022

Trans-cinnamic acid and p-coumaric are valuable intermediates in the synthesis of flavonoids widely employed food, flavor pharmaceutical industries. These products can be produced by deamination L-phenylalanine L-tyrosine catalyzed phenylalanine ammonia lyase or tyrosine lyase. Phenylalanine ammonia-lyase (PAL, EC 4.3.1.5) from Rhodotorula glutinis do not exhibit strong substrate specificity co...

In this study, silver nanoparticles were chemically synthesized and deposited on glass substrates using a reducing agent of sucrose, at 50°C. Different characterizations including atomic force microscopy (AFM), field emission scanning electron microscopy (FESEM), and Raman spectroscopy were obtained to study silvery substrates. Then, the silvery substrates were used as the SERS substrates to de...

Journal: :iranian red crescent medical journal 0
ziba soltani genomic research center, shahid beheshti university of medical sciences, tehran, ir iran fatemeh karami department of medical genetics, school of medicine, tehran university of medical sciences, tehran, ir iran vahidreza yassaee genomic research center, shahid beheshti university of medical sciences, tehran, ir iran feyzollah hashemi gorji genomic research center, shahid beheshti university of medical sciences, tehran, ir iran mahdieh talebzadeh genomic research center, shahid beheshti university of medical sciences, tehran, ir iran mohammad miryounesi genomic research center, shahid beheshti university of medical sciences, tehran, ir iran; genomic research center, shahid beheshti university of medical sciences, tehran, ir iran. tel: +98-2122439959, fax: +98-2122439961

conclusions this finding may help improve early detection, differential diagnosis, genetic counseling, and even treatment of patients with pku. introduction phenylketonuria (pku) is an autosomal recessive inborn error of phenylalanine metabolism, which is caused by mutation in phenylalanine hydroxylase (pah) gene. most of the pah mutations are missense mutations (67%), which are followed by sma...

Journal: :jundishapur journal of chronic disease care 0
houshang alijani renani faculty of nursing and midwifery, ahvaz jundishapur university of medical sciences, ahvaz, ir iran akram hemmatipour faculty of nursing and midwifery, ahvaz jundishapur university of medical sciences, ahvaz, ir iran ashrafalsadat hakim faculty of nursing and midwifery, ahvaz jundishapur university of medical sciences, ahvaz, ir iran majid aminzadeh diabetes research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran; diabetes research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran. tel: +98-6114433715

introduction phenylketonuria (pku) is a congenital metabolic disorder of phenylalanine, if which, the diet is not to be followed exactly, it can lead to progressive mental retardation. the purpose of this study was to investigate the effect of face to face and non-face to face trainings by parental on controlling serum phenylalanine levels in the children with phenylketonuria. materials and met...

2015
Joshua R. Widhalm Michael Gutensohn Heejin Yoo Funmilayo Adebesin Yichun Qian Longyun Guo Rohit Jaini Joseph H. Lynch Rachel M. McCoy Jacob T. Shreve Jyothi Thimmapuram David Rhodes John A. Morgan Natalia Dudareva

In addition to proteins, L-phenylalanine is a versatile precursor for thousands of plant metabolites. Production of phenylalanine-derived compounds is a complex multi-compartmental process using phenylalanine synthesized predominantly in plastids as precursor. The transporter(s) exporting phenylalanine from plastids, however, remains unknown. Here, a gene encoding a Petunia hybrida plastidial c...

Journal: :Nature Biotechnology 1985

Journal: :The Journal of biological chemistry 1990
R Shiman S H Jones D W Gray

The mechanism of phenylalanine regulation of rat liver phenylalanine hydroxylase was studied. We show that phenylalanine "activates" phenylalanine hydroxylase, converting it from an inactive to active form, by binding at a true allosteric regulatory site. One phenylalanine molecule binds per enzyme subunit; it remains at this site during catalytic turnover and, while there, cannot be hydroxylat...

In the present study, the application for the removal of phenylalanine by using two nano sorbents, namely, cetyltrimethylammonium bromide –Coated and BKC (benzal-conium chloride)-Coated Fe3O4 nanoparticles was investigated. Solid-phase extraction (SPE) and ultra violet–visible spectroscopy were used for studying the removal ability of each nano-sorbent in this study. Scanning Electron Microscop...

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