Reiss Ernst, Schlesier Bernhard, Brandt Wolfgang
Federal Centre for Breeding Research on Cultivated Plants, Institute of Resistance Research and Pathogendiagnostics, Theodor-Roemer-Weg 4, D-06449 Aschersleben, Germany.
Phytochemistry. 2006 Sep;67(17):1856-64. doi: 10.1016/j.phytochem.2006.06.014. Epub 2006 Jul 31.
Barley plants are known to produce various PR-5 proteins. Transcripts encoding eight different barley PR-5 proteins (TLPs 1-8, TLP for thaumatin-like protein) were identified and cloned - seven from infected leaves and one from developing grains. Here, we describe the cDNA sequences of four of these TLP isoforms. Moreover, the TLPs from the infected leaves (TLPs 1, 2, and TLPs 4-8) were subjected to MALDI-TOF mass spectrometric measurements that resulted in protein fragments consistent with their deduced peptide sequences. Multiple sequence alignment analysis revealed that the TLPs in barley fall into two groups: long-chain proteins (TLPs 5-8) having 16 cysteine residues and short-chain proteins (TLPs 1-4) with only 10 cysteine residues. Finally, modelling experiments highlighted the effects of sequence differences between the TLP isoforms in terms of their secondary structures and their molecular electrostatic potentials. We propose that these sequence differences have implications for the target preferences of the different isomers.
已知大麦植株会产生多种病程相关蛋白5(PR - 5)。鉴定并克隆了编码八种不同大麦PR - 5蛋白(TLP 1 - 8,TLP即类甜蛋白)的转录本——七种来自受感染叶片,一种来自发育中的谷粒。在此,我们描述其中四种TLP同工型的cDNA序列。此外,对来自受感染叶片的TLP(TLP 1、2以及TLP 4 - 8)进行了基质辅助激光解吸电离飞行时间质谱测量,结果得到的蛋白片段与其推导的肽序列一致。多序列比对分析表明,大麦中的TLP可分为两组:具有16个半胱氨酸残基的长链蛋白(TLP 5 - 8)和仅有10个半胱氨酸残基的短链蛋白(TLP 1 - 4)。最后,建模实验突出了TLP同工型之间序列差异对其二级结构和分子静电势的影响。我们认为这些序列差异对不同异构体的靶标偏好具有影响。