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1.
Int J Mol Sci ; 20(22)2019 Nov 06.
Article in English | MEDLINE | ID: mdl-31698762

ABSTRACT

Muramidases/lysozymes are important bio-molecules, which cleave the glycan backbone in the peptidoglycan polymer found in bacterial cell walls. The glycoside hydrolase (GH) family 22 C-type lysozyme, from the folivorous bird Opisthocomus hoazin (stinkbird), was expressed in Aspergillus oryzae, and a set of variants was produced. All variants were enzymatically active, including those designed to probe key differences between the Hoatzin enzyme and Hen Egg White lysozyme. Four variants showed improved thermostability at pH 4.7, compared to the wild type. The X-ray structure of the enzyme was determined in the apo form and in complex with chitin oligomers. Bioinformatic analysis of avian GH22 amino acid sequences showed that they separate out into three distinct subgroups (chicken-like birds, sea birds and other birds). The Hoatzin is found in the "other birds" group and we propose that this represents a new cluster of avian upper-gut enzymes.


Subject(s)
Birds/metabolism , Muramidase/chemistry , Upper Gastrointestinal Tract/enzymology , Amino Acid Sequence , Animals , Aspergillus/metabolism , Cell Wall/metabolism , Hydrogen-Ion Concentration , Models, Molecular , Phylogeny , Polysaccharides/chemistry , Static Electricity
2.
J Physiol Pharmacol ; 58 Suppl 6: 23-52, 2007 Dec.
Article in English | MEDLINE | ID: mdl-18212399

ABSTRACT

Melatonin, an indole formed enzymatically from L-tryptophan, is the most versatile and ubiquitous hormone molecule produced not only in all animals but also in some plants. This review focuses on the role of melatonin in upper portion of gastrointestinal tract (GIT), including oral cavity, esophagus, stomach and duodenum, where this indole is generated and released into the GIT lumen and into the portal circulation to be uptaken, metabolized by liver and released with bile into the duodenum. The biosynthetic steps of melatonin with two major rate limiting enzymes, arylalkylamine-N-acetyltransferase (AA-NAT) and hydroxyindole-O-methyltransferase (HIOMT), transforming tryptophan to melatonin, originally identified in pinealocytes have been also detected in entero-endocrine (EE) cells of GIT wall, where this indole may act via endocrine, paracrine and/or luminal pathway through G-protein coupled receptors. Melatonin in GIT was shown to be generated in about 500 times larger amounts than it is produced in pineal gland. The production of melatonin by pineal gland shows circadian rhythm with high night-time peak, especially at younger age, followed by the fall during the day-light time. As a highly lipophilic substance, melatonin reaches all body cells within minutes, to serve as a convenient circadian timing signal for alteration of numerous body functions.. Following pinealectomy, the light/dark cycle of plasma melatonin levels disappears, while its day-time blood concentrations are attenuated but sustained mainly due to its release from the GIT. After oral application of tryptophan, the plasma melatonin increases in dose-dependent manner both in intact and pinealectomized animals, indicating that extrapineal sources such as GIT rather than pineal gland are the major producers of this indole. In the upper portion of GIT, melatonin exhibits a wide spectrum of activities such as circadian entrainment, free radicals scavenging activity, protection of mucosa against various irritants and healing of various GIT lesions such as stomatitis, esophagitis, gastritis and peptic ulcer. This review concentrates on the generation and pathophysiological implication of melatonin in upper GIT.


Subject(s)
Antioxidants/metabolism , Melatonin/metabolism , Upper Gastrointestinal Tract/metabolism , Acetylserotonin O-Methyltransferase/metabolism , Animals , Antioxidants/chemistry , Arylalkylamine N-Acetyltransferase/metabolism , Eating/physiology , Gastrointestinal Diseases/drug therapy , Gastrointestinal Diseases/metabolism , Gastrointestinal Diseases/physiopathology , Humans , Intestinal Mucosa/metabolism , Liver/physiology , Melatonin/chemistry , Melatonin/therapeutic use , Mouth Diseases/drug therapy , Mouth Diseases/metabolism , Mouth Diseases/physiopathology , Pineal Gland/enzymology , Pineal Gland/metabolism , Pineal Gland/physiology , Tryptophan/metabolism , Upper Gastrointestinal Tract/enzymology
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