Glycoside hydrolase gene transcription by Alicyclobacillus acidocaldarius during growth on wheat arabinoxylan and monosaccharides: a proposed xylan hydrolysis mechanism

被引:3
作者
Lee, Brady D. [1 ,2 ,4 ]
Apel, William A. [1 ]
Sheridan, Peter P. [2 ]
DeVeaux, Linda C. [3 ]
机构
[1] Biol Syst Dept, Idaho Natl Lab, POB 1625, Idaho Falls, ID 83415 USA
[2] Idaho State Univ, Dept Biol Sci, Campus Box 8007, Pocatello, ID 83209 USA
[3] New Mexico Inst Min & Technol, Dept Biol, 801 Leroy Pl, Socorro, NM 87801 USA
[4] Pacific Northwest Natl Lab, Energy & Environm Directorate, Richland, WA 99354 USA
关键词
Alicyclobacillus acidocaldarius; Wheat arabinoxylan; Glycoside hydrolase; Microarray; ALPHA-AMYLASE; BETA-GALACTOSIDASE; BACILLUS-ACIDOCALDARIUS; LIGNOCELLULOSIC BIOMASS; ORCHARD SOIL; 16S RDNA; SP A4; IDENTIFICATION; SEQUENCE; ENDOGLUCANASE;
D O I
10.1186/s13068-018-1110-3
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Metabolism of carbon bound in wheat arabinoxylan ( WAX) polysaccharides by bacteria requires a number of glycoside hydrolases active toward different bonds between sugars and other molecules. Alicyclobacillus acidocaldarius is a Gram-positive thermoacidophilic bacterium capable of growth on a variety of mono-, di-, oligo-, and polysaccharides. Nineteen proposed glycoside hydrolases have been annotated in the A. acidocaldarius Type Strain ATCC27009/DSM 446 genome. Experiments were performed to understand the effect of monosaccharides on gene expression during growth on the polysaccharide, WAX. Results: Molecular analysis using high-density oligonucleotide microarrays was performed on A. acidocaldarius strain ATCC27009 when growing on WAX. When a culture growing exponentially at the expense of arabinoxylan saccharides was challenged with glucose or xylose, most glycoside hydrolases were downregulated. Interestingly, regulation was more intense when xylose was added to the culture than when glucose was added, showing a clear departure from classical carbon catabolite repression demonstrated by many Gram-positive bacteria. In silico analyses of the regulated glycoside hydrolases, along with the results from the microarray analyses, yielded a potential mechanism for arabinoxylan metabolism by A. acidocaldarius. Glycoside hydrolases expressed by this strain may have broad substrate specificity, and initial hydrolysis is catalyzed by an extracellular xylanase, while subsequent steps are likely performed inside the growing cell. Conclusions: Glycoside hydrolases, for the most part, appear to be found in clusters, throughout the A. acidocaldarius genome. Not all of the glycoside hydrolase genes found at loci within these clusters were regulated during the experiment, indicating that a specific subset of the 19 glycoside hydrolase genes found in A. acidocaldarius were used during metabolism of WAX. While specific functions of the glycoside hydrolases were not tested as part of the research discussed, many of the glycoside hydrolases found in the A. acidocaldarius Type Strain appear to have a broader substrate range than that represented by the glycoside hydrolase family in which the enzymes were categorized.
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