Microspectroscopic imaging of nodulation factor-binding sites on living Vicia sativa roots using a novel bioactive fluorescent nodulation factor

被引:23
作者
Gadella, TWJ
Vereb, G
Hadri, AE
Rohrig, H
Schmidt, J
John, M
Schell, J
Bisseling, T
机构
[1] AGR UNIV WAGENINGEN, DEPT BIOCHEM, NL-6703 HA WAGENINGEN, NETHERLANDS
[2] MAX PLANCK INST BIOPHYS CHEM, DEPT MOL BIOL, D-37077 GOTTINGEN, GERMANY
[3] AGR UNIV WAGENINGEN, DEPT BIOL MOL, WAGENINGEN, NETHERLANDS
[4] MAX PLANCK INST ZUCHTUNGSFORSCH, ABT GENET GRUNDLAGEN PFLANZENZUCHTUNG, D-5000 COLOGNE, GERMANY
基金
匈牙利科学研究基金会;
关键词
D O I
10.1016/S0006-3495(97)78843-X
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A novel bioactive fluorescent nodulation (Nod) factor, NodRlv-IV(BODIPY FL-C-16), has been synthesized by attaching a BODIPY FL-C-16 acyl chain to the primary amino group of chitotetraose deacetylated at the nonreducing terminus by recombinant NodB. The binding of the fluorescent Nod factor to root systems of Vicia sativa was investigated with fluorescence spectral imaging microscopy (FSPIM) and fluorescence ratio imaging microscopy (FRIM). Spatially resolved fluorescence spectra of living and labeled Vicia sativa root systems were measured by FSPIM. Strong autofluorescence, inherent to many plant systems when excited at 488 nm, was corrected for by utilizing the difference in fluorescence emission spectra of the autofluorescence and NodRlv-IV(BODIPY FL-C-16). A methodology is presented to break down the in situ fluorescence emission spectra into spatially resolved autofluorescence and BODIPY FL fluorescence spectra. Furthermore, an FRIM method was developed for correcting autofluorescence in fluorescence micrographs for this system. After autofluorescence correction it was shown that NODRlv-IV(BODIPY FL-C-16) was co root hairs, but was also bound to other parts of the root surface.
引用
收藏
页码:1986 / 1996
页数:11
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