Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

Dual Agarolytic Pathways in a Marine Bacterium, Vibrio sp. Strain EJY3: Molecular and Enzymatic Verification

Authors
Yu, SoraYun, Eun JuKim, Dong HyunPark, So YoungKim, Kyoung Heon
Issue Date
3월-2020
Publisher
AMER SOC MICROBIOLOGY
Keywords
alpha-neoagarooligosaccharide hydrolase; Vibrio sp. strain EJY3; agarolytic beta-galactosidase; agarolytic pathway; agarose; neoagarotetraose; red macroalgae
Citation
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, v.86, no.6
Indexed
SCIE
SCOPUS
Journal Title
APPLIED AND ENVIRONMENTAL MICROBIOLOGY
Volume
86
Number
6
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/57574
DOI
10.1128/AEM.02724-19
ISSN
0099-2240
Abstract
Vibrio sp. strain EJY3 is an agarolytic marine bacterium that catabolizes 3,6-anhydro-L-galactose (AHG), a monomeric sugar unit of agarose. While the AHG catabolic pathway in EJY3 has been discovered recently, the complete agarolytic system of EJY3 remains unclear. We have identified five enzymes, namely, the beta-agarases VejGH50A, VejGH50B, VejGH50C, and VejGH5OD and the alpha-neoagarooligosaccharide (NAOS) hydrolase VejGH117, involved in the agarolytic system of EJY3. Based on the characterization of recombinant enzymes and intracellular metabolite analysis, we found that EJY3 catabolizes agarose via two different agarolytic pathways. Among the four beta-agarases of EJY3, VeiGH50A, VeiGH50B, and VeiGH50C were found to be extracellular agarases, producing mainly neoagarotetraose (NeoDP4) and neoagarobiose. By detecting intracellular NeoDP4 in EJY3 grown on agarose, NeoDP4 was observed being taken up by cells. Intriguingly, intracellular NeoDP4 acted as a branching point for the two different downstream agarolytic pathways. First, via the well-known agarolytic pathway, NeoDP4 was depolymerized into monomeric sugars by the exo-type beta-agarase VejGH5OD and the alpha-NAOS hydrolase VejGH117. Second, via the newly found alternative agarolytic pathway, NeoDP4 was depolymerized into AHG and agarotriose (AgaDP3) by VejGH117, and AgaDP3 then was completely depolymerized into monomeric sugars by sequential reactions of the agarolytic beta-galactosidases (ABG) VejABG and VejGH117. Therefore, by experimentally verifying agarolytic enzymatic activity and transport of NeoDP4 into EJY3 cells, we revealed that EJY3 possesses both the known pathway and the newly discovered alternative pathway that involves alpha-NAOS hydrolase and ABG. IMPORTANCE Agarose is the main polysaccharide of red macroalgae and is composed of galactose and 3,6-anhydro-L-galactose. Many marine bacteria possess enzymes capable of depolymerizing agarose into oligomers and then depolymerizing the oligomers into monomers. Here, we experimentally verified that both a well-known agarolytic pathway and a novel agarolytic pathway exist in a marine bacterium, Vibrio sp. strain EJY3. In agarolytic pathways, agarose is depolymerized mainly into 4-sugar-unit oligomers by extracellular enzymes, which are then transported into cells. The imported oligomers are intracellularly depolymerized into galactose and 3,6-anhydro-L-galactose by two different agarolytic pathways, using different combinations of intracellular enzymes. These results elucidate the depolymerization routes of red macroalgal biomass in the ocean by marine bacteria and provide clues for developing industrial processes for efficiently producing sugars from red macroalgae.
Files in This Item
There are no files associated with this item.
Appears in
Collections
Graduate School > Department of Biotechnology > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Researcher Kim, Kyoung Heon photo

Kim, Kyoung Heon
융합생명공학과
Read more

Altmetrics

Total Views & Downloads

BROWSE