摘要：β-1,3-葡聚糖酶是一种植物病程相关蛋白,在植物抵御病害中有重要作用。本研究以毛竹为实验材料,利用rACE技术,克隆毛竹β-1,3-葡聚糖酶基因的外显子序列,并在β-1,3-葡聚糖酶基因的编码区两端设计引物,以毛竹基因组dNA为模版扩增该基因的内含子序列。序列结果表明,该基因全长1693bp,包含两个外显子和一个内含子,命名为PheGLU(GenBank登录号GU238236)。该基因包含1个996bp的开放阅读框,编码332个氨基酸,相对分子质量为3.541×104da,其等电点pI为6.389,是一个酸性蛋白且分泌到胞外;其中,该蛋白的二级结构中包含35.15%的α-螺旋,21.82%的β-转角,43.03%的延伸链和无规则卷曲等;三级结构同源建模预测显示,它与大麦β-1,3-葡聚糖酶(PdB number:1ghsA)具有80.4%的同源性;聚类分析显示,该基因序列与已报道的其它植物具有较的高氨基酸序列同源性。本研究为进一步鉴定毛竹β-1,3-葡聚糖酶基因的抗真菌病害能力奠定了基础。

摘要：[ Objective] The aim was to study pretreatment of ultrasound enhancing dilute H2SO4 on cellulase activity of corn straw liquid fermentation and explore the pretretment＇ s optimal conditions. [ Method ] By using orthogonal test, the pretretment of ultrasound enhancing dilute H2SO4 on corn straw was studied, then straw was fermented as the sole carbon source. Finally, the cellulase activity in extracellular fermentation broth was determined. [result] The results showed that cellulase activity in extracellular broth was greatest under the conditions of acid bath time 3 h, acid concentration 3.5%, ultrasonic power 150 W, and ultrasonic time 5 h. They were FPA 15.82 U/ml, Cx 39.9 U/ml, 13-Giu 55.94 U/ml respectively. [ Conclusion] Under the above conditions, extracellular cellulase production has a high stability.

摘要：[Objective] The aim was to obtain the full-length cdNA sequence of dunaliella parva β-actin gene.[Method] Based on the highly conserved amino acid regions of known β-actin,a pair of degenerate primers was synthesized to amplify 533 bp cdNA sequences in dunaliella ***,the 5＇ genomic dNA and 3＇ cdNA sequences were obtained by Genome walking and 3＇-rACE technology based on the obtained *** to the sequences of the 5＇-termini and 3＇-termini,specific primers were synthesized to obtain the full-length cdNA.[result] The full-length β-actin cdNA included 1 137 bp open reading frame（OrF）,617 bp of 3＇ noncoding *** analysis indicated that the highest similarity was found between dunaliella parva and dunaliella *** dunaliella parva β-actin also showed wide similarity with other algae.[Conclusion] The full-length cdNA sequence of *** was firstly obtained,which was highly conserved.