Kimura Tetsuya, Suzuki Hayato, Furuhashi Hirofumi, Aburatani Takeshi, Morimoto Kenji, Sakka Kazuo, Ohmiya Kunio
Faculty of Bioresources, Mie University, Tsu, Japan.
Biosci Biotechnol Biochem. 2002 Feb;66(2):285-92. doi: 10.1271/bbb.66.285.
The gene encoding xylanase F3 (xynF3) was isolated from a genomic library of Aspergillus oryzae KBN616, used for making shoyu koji. The structural part of xynF3 was found to be 1468 bp. The nucleotide sequence of cDNA amplified by RT-PCR showed that the open reading frame of xynF3 was interrupted by ten short introns and encoded 323 amino acids. Direct N-terminal amino acid sequencing showed that the precursor of XynF3 had a signal peptide of 22 amino acids. The predicted amino acid sequence of XynF3 has strong similarity to other family 10 xylanases from fungi. The xynF3 gene was successfully overexpressed in A. oryzae and the XynF3 was purified. The molecular mass of XynF3 estimated on sodium dodecyl sulfate-polyacrylamide gel electrophoresis was 32,000. This was almost the same as the molecular mass of 32,437 calculated from the deduced amino acid sequence. The purified XynF3 showed an optimum activity at pH 5.0 and 58 degrees C. It had a Km of 6.5 mg/ml and a Vmax of 435 micromol x min(-1) x mg(-1) when birch wood xylan was used as a substrate. Expression of the xynF3 gene was analyzed using an Escherichia coli beta-glucuronidase gene as a reporter. The result indicated that xynF3 is expressed in the medium containing wheat bran as a carbon source.
编码木聚糖酶F3(xynF3)的基因是从用于制作酱油曲的米曲霉KBN616的基因组文库中分离出来的。发现xynF3的结构部分为1468 bp。通过RT-PCR扩增的cDNA的核苷酸序列表明,xynF3的开放阅读框被10个短内含子打断,编码323个氨基酸。直接N端氨基酸测序表明,XynF3的前体有一个22个氨基酸的信号肽。XynF3的预测氨基酸序列与其他真菌来源的10族木聚糖酶有很强的相似性。xynF3基因在米曲霉中成功过表达,并且XynF3被纯化。在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳上估计的XynF3的分子量为32,000。这与从推导的氨基酸序列计算出的32,437的分子量几乎相同。纯化的XynF3在pH 5.0和58℃下显示出最佳活性。当以桦木木聚糖为底物时,它的Km为6.5 mg/ml,Vmax为435 μmol·min⁻¹·mg⁻¹。使用大肠杆菌β-葡萄糖醛酸酶基因作为报告基因分析了xynF3基因的表达。结果表明,xynF3在以麦麸作为碳源的培养基中表达。