Literature DB >> 27141939

Distribution of glucan-branching enzymes among prokaryotes.

Eiji Suzuki1, Ryuichiro Suzuki2.   

Abstract

Glucan-branching enzyme plays an essential role in the formation of branched polysaccharides, glycogen, and amylopectin. Only one type of branching enzyme, belonging to glycoside hydrolase family 13 (GH13), is found in eukaryotes, while two types of branching enzymes (GH13 and GH57) occur in prokaryotes (Bacteria and Archaea). Both of these types are the members of protein families containing the diverse specificities of amylolytic glycoside hydrolases. Although similarities are found in the catalytic mechanism between the two types of branching enzyme, they are highly distinct from each other in terms of amino acid sequence and tertiary structure. Branching enzymes are found in 29 out of 30 bacterial phyla and 1 out of 5 archaeal phyla, often along with glycogen synthase, suggesting the existence of α-glucan production and storage in a wide range of prokaryotes. Enormous variability is observed as to which type and how many copies of branching enzyme are present depending on the phylum and, in some cases, even among species of the same genus. Such a variation may have occurred through lateral transfer, duplication, and/or differential loss of genes coding for branching enzyme during the evolution of prokaryotes.

Entities:  

Keywords:  Alpha-glucan; Archaea; Bacteria; Branching enzyme; Carbohydrate-active enzymes; Glycoside hydrolase; Glycosyltransferase

Mesh:

Substances:

Year:  2016        PMID: 27141939     DOI: 10.1007/s00018-016-2243-9

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.261


  75 in total

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Authors:  Junji Noguchi; Kimiko Chaen; Nhuan Thi Vu; Taiki Akasaka; Hiroaki Shimada; Takashi Nakashima; Aiko Nishi; Hikaru Satoh; Toshiro Omori; Yoshimitsu Kakuta; Makoto Kimura
Journal:  Glycobiology       Date:  2011-04-14       Impact factor: 4.313

2.  Vibrio vulnificus glycogen branching enzyme preferentially transfers very short chains: N1 domain determines the chain length transferred.

Authors:  Hye-Jin Jo; Sunghoon Park; Hee-Gon Jeong; Jung-Wan Kim; Jong-Tae Park
Journal:  FEBS Lett       Date:  2015-03-24       Impact factor: 4.124

3.  Crystal structure of full-length Mycobacterium tuberculosis H37Rv glycogen branching enzyme: insights of N-terminal beta-sandwich in substrate specificity and enzymatic activity.

Authors:  Kuntal Pal; Shiva Kumar; Shikha Sharma; Saurabh Kumar Garg; Mohammad Suhail Alam; H Eric Xu; Pushpa Agrawal; Kunchithapadam Swaminathan
Journal:  J Biol Chem       Date:  2010-05-05       Impact factor: 5.157

4.  Diversity of reaction characteristics of glucan branching enzymes and the fine structure of α-glucan from various sources.

Authors:  Takayuki Sawada; Yasunori Nakamura; Takashi Ohdan; Asami Saitoh; Perigio B Francisco; Eiji Suzuki; Naoko Fujita; Takahiro Shimonaga; Shoko Fujiwara; Mikio Tsuzuki; Christophe Colleoni; Steven Ball
Journal:  Arch Biochem Biophys       Date:  2014-08-07       Impact factor: 4.013

5.  Structural basis for branching-enzyme activity of glycoside hydrolase family 57: structure and stability studies of a novel branching enzyme from the hyperthermophilic archaeon Thermococcus kodakaraensis KOD1.

Authors:  Camila R Santos; Celisa C C Tonoli; Daniel M Trindade; Christian Betzel; Hiroki Takata; Takashi Kuriki; Tamotsu Kanai; Tadayuki Imanaka; Raghuvir K Arni; Mário T Murakami
Journal:  Proteins       Date:  2011-02

6.  Self-poisoning of Mycobacterium tuberculosis by targeting GlgE in an alpha-glucan pathway.

Authors:  Rainer Kalscheuer; Karl Syson; Usha Veeraraghavan; Brian Weinrick; Karolin E Biermann; Zhen Liu; James C Sacchettini; Gurdyal Besra; Stephen Bornemann; William R Jacobs
Journal:  Nat Chem Biol       Date:  2010-03-21       Impact factor: 15.040

7.  Bioinformatics of the glycoside hydrolase family 57 and identification of catalytic residues in amylopullulanase from Thermococcus hydrothermalis.

Authors:  Richard Zona; Florent Chang-Pi-Hin; Michael J O'Donohue; Stefan Janecek
Journal:  Eur J Biochem       Date:  2004-07

8.  The unique branching patterns of Deinococcus glycogen branching enzymes are determined by their N-terminal domains.

Authors:  M Palomo; S Kralj; M J E C van der Maarel; L Dijkhuizen
Journal:  Appl Environ Microbiol       Date:  2009-01-09       Impact factor: 4.792

9.  Cloning and nucleotide sequence of a heat-stable amylase gene from an anaerobic thermophile, Dictyoglomus thermophilum.

Authors:  S Fukusumi; A Kamizono; S Horinouchi; T Beppu
Journal:  Eur J Biochem       Date:  1988-05-16

10.  Analysis of the Escherichia coli glycogen gene cluster suggests that catabolic enzymes are encoded among the biosynthetic genes.

Authors:  T Romeo; A Kumar; J Preiss
Journal:  Gene       Date:  1988-10-30       Impact factor: 3.688

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  4 in total

1.  Bound Substrate in the Structure of Cyanobacterial Branching Enzyme Supports a New Mechanistic Model.

Authors:  Mari Hayashi; Ryuichiro Suzuki; Christophe Colleoni; Steven G Ball; Naoko Fujita; Eiji Suzuki
Journal:  J Biol Chem       Date:  2017-02-13       Impact factor: 5.157

Review 2.  Remarkable evolutionary relatedness among the enzymes and proteins from the α-amylase family.

Authors:  Štefan Janeček; Marek Gabriško
Journal:  Cell Mol Life Sci       Date:  2016-05-06       Impact factor: 9.261

3.  Structure and Evolution of Glycogen Branching Enzyme N-Termini From Bacteria.

Authors:  Liang Wang; Qinghua Liu; Junfeng Hu; James Asenso; Michael J Wise; Xiang Wu; Chao Ma; Xiuqing Chen; Jianye Yang; Daoquan Tang
Journal:  Front Microbiol       Date:  2019-01-14       Impact factor: 5.640

Review 4.  Functional Roles of Starch Binding Domains and Surface Binding Sites in Enzymes Involved in Starch Biosynthesis.

Authors:  Casper Wilkens; Birte Svensson; Marie Sofie Møller
Journal:  Front Plant Sci       Date:  2018-11-13       Impact factor: 5.753

  4 in total

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