Scion Research, Private Bag 3020, Rotorua, 3046, New Zealand; School of Biological Sciences, The University of Auckland, Private Bag 92019, Auckland, New Zealand.
Plant J. 2014 Apr;78(2):305-18. doi: 10.1111/tpj.12468. Epub 2014 Mar 26.
Using a functional genomics approach, four candidate genes (PtGT34A, PtGT34B, PtGT34C and PtGT34D) were identified in Pinus taeda. These genes encode CAZy family GT34 glycosyltransferases that are involved in the synthesis of cell-wall xyloglucans and heteromannans. The full-length coding sequences of three orthologs (PrGT34A, B and C) were isolated from a xylem-specific cDNA library from the closely related Pinus radiata. PrGT34B is the ortholog of XXT1 and XXT2, the two main xyloglucan (1→6)-α-xylosyltransferases in Arabidopsis thaliana. PrGT34C is the ortholog of XXT5 in A. thaliana, which is also involved in the xylosylation of xyloglucans. PrGT34A is an ortholog of a galactosyltransferase from fenugreek (Trigonella foenum-graecum) that is involved in galactomannan synthesis. Truncated coding sequences of the genes were cloned into plasmid vectors and expressed in a Sf9 insect cell-culture system. The heterologous proteins were purified, and in vitro assays showed that, when incubated with UDP-xylose and cellotetraose, cellopentaose or cellohexaose, PrGT34B showed xylosyltransferase activity, and, when incubated with UDP-galactose and the same cello-oligosaccharides, PrGT34B showed some galactosyltransferase activity. The ratio of xylosyltransferase to galactosyltransferase activity was 434:1. Hydrolysis of the galactosyltransferase reaction products using galactosidases showed the linkages formed were α-linkages. Analysis of the products of PrGT34B by MALDI-TOF MS showed that up to three xylosyl residues were transferred from UDP-xylose to cellohexaose. The heterologous proteins PrGT34A and PrGT34C showed no detectable enzymatic activity.
利用功能基因组学方法,在火炬松(Pinus taeda)中鉴定出了四个候选基因(PtGT34A、PtGT34B、PtGT34C 和 PtGT34D)。这些基因编码 CAZy 家族 GT34 糖基转移酶,参与细胞壁木葡聚糖和杂合甘露聚糖的合成。从亲缘关系密切的辐射松(Pinus radiata)的木质部特异性 cDNA 文库中分离出三个同源基因(PrGT34A、B 和 C)的全长编码序列。PrGT34B 是拟南芥中两个主要的木葡聚糖(1→6)-α-木糖基转移酶 XXT1 和 XXT2 的同源基因。PrGT34C 是拟南芥中 XXT5 的同源基因,也参与木葡聚糖的糖基化。PrGT34A 是葫芦巴(Trigonella foenum-graecum)半乳糖基转移酶的同源基因,参与半乳甘露聚糖的合成。基因的截断编码序列被克隆到质粒载体中,并在 Sf9 昆虫细胞培养系统中表达。异源蛋白被纯化,体外实验表明,当用 UDP-木糖和纤维四糖、纤维五糖或纤维六糖孵育时,PrGT34B 表现出木糖基转移酶活性,当用 UDP-半乳糖和相同的纤维低聚糖孵育时,PrGT34B 表现出一些半乳糖基转移酶活性。木糖基转移酶与半乳糖基转移酶活性的比值为 434:1。用半乳糖苷酶水解半乳糖基转移酶反应产物表明形成的键为α键。用 MALDI-TOF MS 对 PrGT34B 的产物进行分析表明,多达三个木糖基从 UDP-木糖转移到纤维六糖上。异源蛋白 PrGT34A 和 PrGT34C 没有表现出可检测的酶活性。