University of Belgrade - Institute for Multidisciplinary research, Kneza Višeslava 1, Belgrade 11000, Serbia.
Department of Physics, Norwegian University of Science and Technology (NTNU), N-7491 Trondheim, Norway.
Spectrochim Acta A Mol Biomol Spectrosc. 2023 Dec 15;303:123269. doi: 10.1016/j.saa.2023.123269. Epub 2023 Aug 16.
In situ fluorescence measurements have been used to investigate relative amounts of blue-green pigments and their distributions in plant leaves from Euphorbia pulcherrima. Advantage was taken from the fact that this species has white leaves on the top, with low pigment concentrations, and green leaves on the stem with ordinary pigment concentrations. Excitation- and emission spectra below 410 nm from white leaves, where pigment absorption is low, are not distorted by self-absorption. Absorption- and reflection spectra from white and green leaves were measured using a spectrophotometer equipped with an integrating sphere. The absorption spectra were used to correct recorded fluorescence spectra for self-absorption. Self-absorption corrected photosystem fluorescence from green leaves, modeling light transmission in leaf tissue exponentially, matches to the excitation/emission spectra from white leaves, apart from small differences due to the pigment concentrations and selective scattering. The introduced exponentially decaying transmission relation also predicts that the ratio of excitation spectra from a white and green leaf is in proportion to the absorption spectrum of the green leaf, which was validated for Photosystem II particle fluorescence. This relation was also used to find a scaled absorption spectrum responsible for blue-green emission, which was assumed to originate from lignin. Excitation/emission spectra of the blue-green fluorescence were decomposed into five components and their relative amounts from adaxial and abaxial sides of the leaves have been quantified. Fluorescence lifetime measurements of the leaves, upon 403 nm excitation, revealed three decay times corresponding to the lignin fluorophores emitting in blue and green spectral region, and indicated that emissions at 500 and 550 nm may originate from the same fluorophore residing in the two physically different environments.
已采用原位荧光测量法来研究大丽花花叶中蓝绿素的相对含量及其分布情况。该方法具有一定优势,因为大丽花的顶叶为白色,色素浓度低,而茎上的叶片为绿色,色素浓度正常。在白色叶片(色素吸收率低)中,低于 410nm 的激发和发射光谱不会受到自吸收的影响。使用配备积分球的分光光度计测量了白色和绿色叶片的吸收和反射光谱。吸收光谱用于校正自吸收后的荧光光谱。通过对绿色叶片的荧光进行修正,将其建模为叶片组织中光的指数传输,其与白色叶片的激发/发射光谱相匹配,除了由于色素浓度和选择性散射而导致的微小差异。引入的指数衰减传输关系还预测,白色和绿色叶片的激发光谱之比与绿色叶片的吸收光谱成比例,这在 Photosystem II 粒子荧光中得到了验证。该关系还用于找到负责蓝绿荧光的比例吸收光谱,该光谱假定源自木质素。将蓝绿荧光的激发/发射光谱分解为五个分量,并量化了叶片腹背两面的相对含量。对叶片进行 403nm 激发的荧光寿命测量揭示了三个衰减时间,分别对应于在蓝绿光谱区域发射的木质素荧光团,表明在 500nm 和 550nm 处的发射可能源自同一荧光团,该荧光团存在于两种物理性质不同的环境中。