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Cloning, purification and preliminary crystallographic analysis of Ara127N, a GH127 β‐L‐arabinofuranosidase from Geobacillus stearothermophilus T6
Author(s) -
Lansky Shifra,
Salama Rachel,
Dann Roie,
Shner Izhak,
Manjasetty Babu A.,
Belrhali Hassan,
Shoham Yuval,
Shoham Gil
Publication year - 2014
Publication title -
acta crystallographica section f
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.572
H-Index - 37
ISSN - 2053-230X
DOI - 10.1107/s2053230x14012680
Subject(s) - geobacillus stearothermophilus , orthorhombic crystal system , chemistry , stereochemistry , enzyme , crystallography , crystal structure , monoclinic crystal system , biochemistry , thermophile
The L‐arabinan utilization system of Geobacillus stearothermophilus T6 is composed of five transcriptional units that are clustered within a 38 kb DNA segment. One of the transcriptional units contains 11 genes, the last gene of which ( araN ) encodes a protein, Ara127N, that belongs to the newly established GH127 family. Ara127N shares 44% sequence identity with the recently characterized HypBA1 protein from Bifidobacterium longum and thus is likely to function similarly as a β‐L‐arabinofuranosidase. β‐L‐Arabinofuranosidases are enzymes that hydrolyze β‐L‐arabinofuranoside linkages, the less common form of such linkages, a unique enzymatic activity that has been identified only recently. The interest in the structure and mode of action of Ara127N therefore stems from its special catalytic activity as well as its membership of the new GH127 family, the structure and mechanism of which are only starting to be resolved. Ara127N has recently been cloned, overexpressed, purified and crystallized. Two suitable crystal forms have been obtained: one (CTP form) belongs to the monoclinic space group P 2 1 , with unit‐cell parameters a = 104.0, b = 131.2, c = 107.6 Å, β = 112.0°, and the other (RB form) belongs to the orthorhombic space group P 2 1 2 1 2 1 , with unit‐cell parameters a = 65.5, b = 118.1, c = 175.0 Å. A complete X‐ray diffraction data set has been collected to 2.3 Å resolution from flash‐cooled crystals of the wild‐type enzyme (RB form) at −173°C using synchrotron radiation. A selenomethionine derivative of Ara127N has also been prepared and crystallized for multi‐wavelength anomalous diffraction (MAD) experiments. Crystals of selenomethionine Ara127N appeared to be isomorphous to those of the wild type (CTP form) and enabled the measurement of a three‐wavelength MAD diffraction data set at the selenium absorption edge. These data are currently being used for detailed three‐dimensional structure determination of the Ara127N protein.