Affiliation:
1. Department of Microbiology and Cell Sciences, University of Florida, Gainesville, Florida 32611
Abstract
ABSTRACT
Paenibacillus
sp. strain JDR-2, an aggressively xylanolytic bacterium isolated from decaying sweet gum wood, secretes a multimodular glycohydrolase family GH10 endoxylanase (XynA1) anchored to the cell surface. The gene encoding XynA1 is part of a xylan utilization regulon that includes an aldouronate utilization gene cluster with genes encoding a GH67 α-glucuronidase (AguA), a GH10 endoxylanase (XynA2), and a GH43 arabinofuranosidase/β-xylosidase (XynB). Here we show that this
Paenibacillus
sp. strain is able to utilize methylglucuronoxylose (MeGAX
1
), an aldobiuronate product that accumulates during acid pretreatment of lignocellulosic biomass, and methylglucuronoxylotriose (MeGAX
3
), the product of the extracellular XynA1 acting on methylglucuronoxylan (MeGAX
n
). The average rates of utilization of MeGAX
n
, MeGAX
1
, and MeGAX
3
were 149.8, 59.4, and 54.3 μg xylose equivalents·ml
−1
·h
−1
, respectively, and were proportional to the specific growth rates on the substrates. AguA was active with MeGAX
1
and MeGAX
3
, releasing 4-
O
-methyl-
d
-glucuronate α-1,2 linked to a nonreducing terminal xylose residue. XynA2 converted xylotriose, generated by the action of AguA on MeGAX
3
, to xylose and xylobiose. The ability to utilize MeGAX
1
provides a novel metabolic potential for bioconversion of acid hydrolysates of lignocellulosics. The 2.8-fold-greater rate of utilization of polymeric MeGAX
n
than that of MeGAX
3
indicates that there is coupling of extracellular depolymerization, assimilation, and intracellular metabolism, allowing utilization of lignocellulosics with minimal pretreatment. Along with adjacent genes encoding transcriptional regulators and ABC transporter proteins, the
aguA
and
xynA2
genes in the cluster described above contribute to the efficient utilization of aldouronates derived from dilute acid and/or enzyme pretreatment protocols applied to the conversion of hemicellulose to biofuels and chemicals.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Reference37 articles.
1. Betts, W. B., R. K. Dart, A. S. Ball, and S. L. Pedlar. 1991. Biosynthesis and structure of lignocellulose, p. 139-355. In W. B. Betts, (ed.), Biodegradation of natural and synthetic materials. Springer Verlag, Berlin, Germany.
2. Complete Fermentation of Xylose and Methylglucuronoxylose Derived from Methylglucuronoxylan by
Enterobacter asburiae
Strain JDR-1
3. Biely, P., M. Vrsanska, M. Tenkanen, and D. Kluepfel. 1997. Endo-beta-1,4-xylanase families: differences in catalytic properties. J. Biotechnol.57:151-166.
4. Biely, P., J. Hirsch, D. C. la Grange, W. H. van Zyl, and B. A. Prior. 2000. A chromogenic substrate for a beta-xylosidase-coupled assay of alpha-glucuronidase. Anal. Biochem.286:289-294.
5. Blumenkrantz, N., and G. Asboe-Hansen. 1973. New method for quantitative determination of uronic acids. Anal. Biochem.54:484-489.
Cited by
18 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献