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园艺学报 ›› 2017, Vol. 44 ›› Issue (5): 911-920.doi: 10.16420/j.issn.0513-353x.2016-0624

• 研究论文 • 上一篇    下一篇

利用红外光谱研究‘凤丹白’牡丹花瓣伸展过程中物质变化

李秀丽1,*,陈法志1,戢小梅1,陈 镇1,戴志刚2,杨 阳1,王 燕1   

  1. (1武汉市农业科学技术研究院林业果树科学研究所,武汉 430075;2湖北省耕地质量与肥料工作总站,武汉 430070)
  • 出版日期:2017-05-25 发布日期:2017-05-25

Application of Infrared Spectroscopy to Study on Substance Change in the Process of Petal Extending of Paeonia ostii‘Fengdanbai’

LI Xiuli1,*,CHEN Fazhi1,JI Xiaomei1,CHEN Zhen1,DAI Zhigang2,YANG Yang1,and WANG Yan1,*   

  1. (1Wuhan Academy of Agricultural Science and Technology Forestry and Fruit Tree Research Insititute,Wuhan 430075,China;2Hubei Provincial General Station of Arable Land Quality and Fertilizer,Wuhan 430070,China)
  • Online:2017-05-25 Published:2017-05-25

摘要: 为了明确花瓣的伸展机制,以‘凤丹白’牡丹(Paeonia ostii)为研究对象,借助傅里叶变换红外光谱(Fourier Transformation Infrared Spectroscopy,FTIR)及高斯多峰拟合,分析蕾期、初开期和盛开期花瓣的波谱特征及蛋白质二级结构的差异性。主要结果如下:随着花朵开放花瓣伸展,777、1 105、1 155、1 243、1 447、1 651、1 740、2 853和2 926 cm-1处的振动峰振动依次增强,表明磷脂质、核酸、脂类和蛋白质等代谢物质随花瓣的伸展逐渐增强;且蕾期1 030 cm-1处的振动峰在花开后移至1 060 cm-1,表明蕾期花瓣细胞壁多糖以甘露聚糖为主,花朵开放后则以阿拉伯糖为主。蛋白质中甲基基团含量(A 2 951 cm-1/A 2 858 cm-1)出现平稳下降的趋势,初开期比蕾期减少7.97%,盛开期减少13.38%;糖蛋白的变化(A 1 083 cm-1/A 1 547 cm-1)也呈现下降趋势,推测‘凤丹白’牡丹是通过蛋白质糖基化作用调控花瓣的伸展过程。对氨基Ⅰ区域(1 600 ~ 1 700 cm-1)高斯多峰拟合数据显示,各阶段花瓣中均含有果胶相连的β–折叠、β–折叠、无规卷曲、α–螺旋及环与转角;α–螺旋、β–折叠及无规卷曲所占比例在花瓣伸展过程中呈现增长趋势,表明蕾期花瓣通过降低α–螺旋应对缺水造成的生理胁迫,并可以利用ATP合成花瓣生长发育所需的物质;花瓣通过形成更多功能域较多的蛋白质,有效调控花瓣伸展时复杂的生物化学过程。

关键词: &lsquo, 凤丹白&rsquo, 牡丹;花瓣;傅里叶变换红外光谱(FTIR);高斯多峰拟合;蛋白质二级结构

Abstract: In order to understand the petal extension mechanism,both FTIR(fourier transformation infrared spectroscopy)and Guassian multi-peak fitting were used to explore spectrum properties and protein secondary structure differences of Paeonia ostii‘Fengdanbai’petal at the flower-bud,initiating bloom and bloom periods. The main results were as follows:The peak intensity at 777,1 105,1 155,1 243,1 447,1 651,1 740,2 853 and 2 926 cm-1 were enhanced in sequence with flowering,indicating that the metabolism products such as phospholipids,nucleic acids,lipids,proteins were increased during the process of flowering. A shift from 1 030 cm-1 to 1 060 cm-1 was observed in petal at flower-bud period and bloom period,which showed that cell wall polysaccharides of petal were glucomannan and arabinan,respectively. As compared with the petal at flower-bud period,the number of methyl groups in protein(A 2 951 cm-1/A 2 858 cm-1)of petal decrease by 7.97% and 13.38% at initiating bloom period and bloom period,respectively. The variation in glycoprotein of the samples(A 1 083 cm-1/A 1 547 cm-1)showed a downward trend after flowering,it could speculate out that protein regulate the petal extension by glycosylation in‘Fengdanbai’. The result of Guassian multi-peak fitting for the amideⅠregion(1 600–1 700 cm-1)indicated that the petal contained β-sheet + side chain + pectin,β-sheet,random coil,α-helix and loop + turn of secondary protein structure at different stages. And the α-helix,β-sheet and random coil showed an increase trend after flowering. The result indicated that the presence of low amounts of α-helix domains in petal at flower-bud period might compensate for reducing protein-water hydrogen band caused by lack of water. And also ATP was modified,which would provide the material base for petal-extension. The protein would regulate the complex biochemical processes in petal extension by forming more functional domains. The research results provided theoretical references for the substance change and the protein regulation on extension mechanism of petal.

Key words: Paeonia ostii‘Fengdanbai’, petal, fourier transformation infrared spectroscopy(FTIR), Guassian multi-peak fitting, protein secondary structure

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