Label-free visualization of lignin deposition in loquats using complementary stimulated and spontaneous Raman microscopy

Nan Zhu , Yifan Yang , Minbiao Ji , Di Wu , Kunsong Chen

Horticulture Research ›› 2019, Vol. 6 ›› Issue (1) : 72

PDF (2185KB)
Horticulture Research ›› 2019, Vol. 6 ›› Issue (1) :72 DOI: 10.1038/s41438-019-0153-3
Article
research-article
Label-free visualization of lignin deposition in loquats using complementary stimulated and spontaneous Raman microscopy
Author information +
History +
PDF (2185KB)

Abstract

The lignification triggered by biotic or abiotic stresses hardens fruits and vegetables and eventually influences their consumer appeal. Extensive prior efforts have been made to unveil the underlying mechanism of flesh lignification, primarily focused on its physicochemical and molecular biological properties. Nevertheless, most of these studies used destroyed and homogenized bulk tissues as analytes; as a result, potentially valuable spatial information was lost. In this study, the deposition of lignin in loquat flesh during lignification was visualized from the tissue level to the single-cell level by combining the advantages of stimulated Raman scattering (SRS) and spontaneous Raman microscopy using label-free in situ molecular imaging. SRS has the advantages of being fast and providing large-area chemical imaging to reveal the spatial heterogeneity of lignin and cell wall polysaccharide distribution in loquat flesh. After 2 days of storage at 0 °C, increased lignins were observed by large-area SRS imaging. In addition, microscopic SRS images of the flesh cells indicated that the increased lignins were trapped in the cell corner (CC) and middle lamella (ML). Furthermore, the compositional and structural features of lignified cells (LCs), CC and ML of loquat flesh were investigated by spontaneous Raman microscopy, and the results showed that the LCs were a combination of lignin, cellulose, and hemicellulose, whereas CC and ML showed only deposited lignin and pectin without cross-linked cellulose and hemicellulose. This result further suggests that the lignins in the CC and ML regions of loquats were later synthesized alone during postharvest storage. This innovative combination of SRS and spontaneous Raman microscopy allows the label-free macroscale and fine chemical imaging of plant cell walls and will enhance our fundamental understanding of the structures and functions of the plant cell wall.

Cite this article

Download citation ▾
Nan Zhu, Yifan Yang, Minbiao Ji, Di Wu, Kunsong Chen. Label-free visualization of lignin deposition in loquats using complementary stimulated and spontaneous Raman microscopy. Horticulture Research, 2019, 6 (1) : 72 DOI:10.1038/s41438-019-0153-3

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Li, X., Xu, C., Korban, S. & Chen, K. Regulatory mechanisms of textural changes in ripening fruits. Crit. Rev. Plant Sci. 29, 222-243 (2010).

[2]

Yang, S. et al. Expression of expansin genes during postharvest lignification and softening of ‘Luoyangqing’ and ‘Baisha’ loquat fruit under different storage conditions. Postharvest Biol. Technol. 49, 46-53 (2008).

[3]

Uluisik, S. et al. Genetic improvement of tomato by targeted control of fruit softening. Nat. Biotechnol. 34, 950 (2016).

[4]

Centeno, D. C. et al. Malate plays a crucial role in starch metabolism, ripening, and soluble solid content of tomato fruit and affects postharvest softening. Plant Cell 23, 162-184 (2011).

[5]

Zhang, A.-d et al. Transcriptome analysis identifies a zinc finger protein regulating starch degradation in kiwifruit. Plant Physiol. 178, 850-863 (2018).

[6]

Taglienti, A., Massantini, R., Botondi, R., Mencarelli, F. & Valentini, M. Postharvest structural changes of Hayward kiwifruit by means of magnetic resonance imaging spectroscopy. Food Chem. 114, 1583-1589 (2009).

[7]

Johnston, J. W., Hewett, E. W. & Hertog, M. L. A. T. M. Postharvest softening of apple (Malus domestica) fruit: a review. N. Z. J. Crop Hortic. Sci. 30, 145-160 (2002).

[8]

Szymanska-Chargot, M. et al. Raman imaging of changes in the polysaccharides distribution in the cell wall during apple fruit development and senescence. Planta 243, 935-945 (2016).

[9]

Hayama, H., Ito, A., Moriguchi, T. & Kashimura, Y. Identification of a new expansin gene closely associated with peach fruit softening. Postharvest Biol. Technol. 29, 1-10 (2003).

[10]

Zhu, N., Huang, W. N., Wu, D., Chen, K. S. & He, Y. Quantitative visualization of pectin distribution maps of peach fruits. Sci. Rep. 7, https://doi.org/10.1038/s41598-017-09817-7 (2017).

[11]

Zeng, J. K. et al. EjAP2-1, an AP2/ERF gene, is a novel regulator of fruit lignification induced by chilling injury, via interaction with EjMYB transcription factors. Plant Biotechnol. J. 13, 1325-1334 (2015).

[12]

Mustafa, M. A., Ali, A., Seymour, G. & Tucker, G. Delayed pericarp hardening of cold stored mangosteen (Garcinia mangostana L.) upon pre-treatment with the stress hormones methyl jasmonate and salicylic acid. Sci. Hortic. 230, 107-116 (2018).

[13]

Kamdee, C. et al. Regulation of lignin biosynthesis in fruit pericarp hardening of mangosteen (Garcinia mangostana L.) after impact. Postharvest Biol. Technol. 97, 68-76 (2014).

[14]

Ge, H. et al. EjNAC3 transcriptionally regulates chilling-induced lignification of loquat fruit via physical interaction with an atypical CAD-like gene. J. Exp. Bot. 68, 5129-5136 (2017).

[15]

Cai, C., Xu, C., Li, X., Ferguson, I. & Chen, K. Accumulation of lignin in relation to change in activities of lignification enzymes in loquat fruit flesh after harvest. Postharvest Biol. Technol. 40, 163-169 (2006).

[16]

Cai, C. et al. Low temperature conditioning reduces postharvest chilling injury in loquat fruit. Postharvest Biol. Technol. 41, 252-259 (2006).

[17]

Wang, P. et al. Ethylene signal transduction elements involved in chilling injury in non-climacteric loquat fruit. J. Exp. Bot. 61, 179-190 (2010).

[18]

Barros, J., Serk, H., Granlund, I. & Pesquet, E. The cell biology of lignification in higher plants. Ann. Bot. 115, 1053-1074 (2015).

[19]

Boerjan, W., Ralph, J. & Baucher, M. Lignin biosynthesis. Annu. Rev. Plant Biol. 54, 519-546 (2003).

[20]

Vanholme, R., Demedts, B., Morreel, K., Ralph, J. & Boerjan, W. Lignin biosynthesis and structure. Plant Physiol. 153, 895-905 (2010).

[21]

Zheng, Y., Li, S. & Xi, Y. Changes of cell wall substances in relation to flesh woodiness in cold stored loquat fruits. Acta Photophysiol. Sin. 26, 306-310 (2000).

[22]

Bunsiri, A., Ketsa, S. & Paull, R. E. Phenolic metabolism and lignin synthesis in damaged pericarp of mangosteen fruit after impact. Postharvest Biol. Technol. 29, 61-71 (2003).

[23]

Cai, C., Gong, M., Li, X., Junliang, L. & Chen, K. Texture changes and regulation of postharvest loquat fruit. Acta Hortic. Sin. 33, 731-736 (2006).

[24]

Shan, L. L. et al. Characterization of cDNAs associated with lignification and their expression profiles in loquat fruit with different lignin accumulation. Planta 227, 1243-1254 (2008).

[25]

Xu, Q. et al. Activator- and repressor-type MYB transcription factors are involved in chilling injury induced flesh lignification in loquat via their interactions with the phenylpropanoid pathway. J. Exp. Bot. 65, 4349-4359 (2014).

[26]

Zeng, J. K. et al. Regulation of loquat fruit low temperature response and lignification involves interaction of heat shock factors and genes associated with lignin biosynthesis. Plant Cell Environ. 39, 1780-1789 (2016).

[27]

Xu, Q. et al. A NAC transcription factor, EjNAC1, affects lignification of loquat fruit by regulating lignin. Postharvest Biol. Technol. 102, 25-31 (2015).

[28]

Gierlinger, N. & Schwanninger, M. Chemical imaging of poplar wood cell walls by confocal Raman microscopy. Plant Physiol. 140, 1246-1254 (2006).

[29]

Liu, B. et al. Vibrational fingerprint mapping reveals spatial distribution of functional groups of lignin in plant cell wall. Anal. Chem. 87, 9436-9442 (2015).

[30]

Ding, S.-Y. et al. How does plant cell wall nanoscale architecture correlate with enzymatic digestibility?. Science 338, 1055-1060 (2012).

[31]

Prats-Mateu, B., Felhofer, M., de Juan, A. & Gierlinger, N. Multivariate unmixing approaches on Raman images of plant cell walls: new insights or overinterpretation of results?. Plant Methods 14, https://doi.org/10.1186/s13007-018-0320-9 (2018).

[32]

Zhu, N., Wu, D. & Chen, K. Label-free visualization of fruit lignification: Raman molecular imaging of loquat lignified cells. Plant Methods 14, 58 (2018).

[33]

Hänninen, T., Kontturi, E. & Vuorinen, T. Distribution of lignin and its coniferyl alcohol and coniferyl aldehyde groups in Picea abies and Pinus sylvestris as observed by Raman imaging. Phytochemistry 72, 1889-1895 (2011).

[34]

Schreiber, N. et al. G-fibres in storage roots of Trifolium pratense (Fabaceae): tensile stress generators for contraction. Plant J. 61, 854-861 (2010).

[35]

Agarwal, U. P. Raman imaging to investigate ultrastructure and composition of plant cell walls: distribution of lignin and cellulose in black spruce wood (Picea mariana). Planta 224, 1141-1153 (2006).

[36]

Gierlinger, N. et al. Cellulose microfibril orientation of Picea abies and its variability at the micron-level determined by Raman imaging. J. Exp. Bot. 61, 587-595 (2010).

[37]

Ozparpucu, M. et al. Unravelling the impact of lignin on cell wall mechanics: a comprehensive study on young poplar trees downregulated for Cinnamyl Alcohol Dehydrogenase (CAD). Plant J. 91, 480-490 (2017).

[38]

Freudiger, C. W. et al. Label-free biomedical imaging with high sensitivity by stimulated Raman scattering microscopy. Science 322, 1857-1861 (2008).

[39]

Liao, C. S. et al. Microsecond scale vibrational spectroscopic imaging by multiplex stimulated Raman scattering microscopy. Light: Sci. Appl. 4, https://doi.org/10.1038/lsa.2015.38 (2015).

[40]

Zhang, D., Wang, P., Slipchenko, M. N. & Cheng, J. X. Fast vibrational imaging of single cells and tissues by stimulated Raman scattering microscopy. Acc. Chem. Res. 47, 2282-2290 (2014).

[41]

Mansfield, J. C. et al. Label-free chemically specific imaging in planta with stimulated Raman scattering microscopy. Anal. Chem. 85, 5055-5063 (2013).

[42]

Zhang, D. L. et al. Quantitative vibrational imaging by hyperspectral stimulated Raman scattering microscopy and multivariate curve resolution analysis. Anal. Chem. 85, 98-106 (2013).

[43]

Littlejohn, G. R. et al. In vivo chemical and structural analysis of plant cuticular waxes using stimulated Raman scattering microscopy. Plant Physiol. 168, 18-28 (2015).

[44]

Agarwal, U. P. 1064 nm FT-Raman spectroscopy for investigations of plant cell walls and other biomass materials. Front. Plant Sci. 5, 490 (2014).

[45]

Agarwal, U. P., Ralph, S. A., Reiner, R. S. & Baez, C. Probing crystallinity of never-dried wood cellulose with Raman spectroscopy. Cellulose 23, 125-144 (2015).

[46]

Zeng, Y. N. et al. In situ label-free imaging of hemicellulose in plant cell walls using stimulated Raman scattering microscopy. Biotechnol. Biofuels 9, https://doi.org/10.1186/s13068-016-0669-9 (2016).

[47]

Chylińska, M., Szymańska-Chargot, M., Deryło, K., Tchórzewska, D. & Zdunek, A. Changing of biochemical parameters and cell wall polysaccharides distribution during physiological development of tomato fruit. Plant Physiol. Biochem. 119, 328 (2017).

[48]

Gwanpua, S. G. et al. Slow softening of Kanzi apples (Malus×domestica L.) is associated with preservation of pectin integrity in middle lamella. Food Chem. 211, 883-891 (2016).

[49]

Chylinska, M., Szymanska-Chargot, M. & Zdunek, A. Imaging of polysaccharides in the tomato cell wall with Raman microspectroscopy. Plant Methods 10, 14 (2014).

[50]

Pan, T.-T., Pu, H. & Sun, D.-W. Insights into the changes in chemical compositions of the cell wall of pear fruit infected by Alternaria alternata with confocal Raman microspectroscopy. Postharvest Biol. Technol. 132, 119-129 (2017).

[51]

Sarkanen, K. V. & Ludwig, C. H. Lignins: Occurrence, Formation, Structure and Reactions (Wiley-Interscience, New York, 1971).

[52]

Barakat, A. et al. The cinnamyl alcohol dehydrogenase gene family in Populus: phylogeny, organization, and expression. BMC Plant Biol. 9, https://doi.org/10.1186/1471-2229-9-26 (2009).

PDF (2185KB)

0

Accesses

0

Citation

Detail

Sections
Recommended

/