Abstract
As the by-products of edible oil production with rich lignin, the reserves of Camellia oleifera shell were abundant and had a great economic value. Lignin was the most important limiting factor during the conversion of plant biomass to pulp or biofuels, which mainly deposited in the stone cells of C. oleifera shells. Thus, its lignin deposition made the function of stone cells in the ripening process of the shell clearer, and provided a theoretical basis for the potential utilization of the biomass of C. oleifera shells. In this study, the paraffin embedding method was used to investigate the development and difference of stone cell in the fruitlet. The lignin deposition characteristics of stone cell were analyzed by the fluorescence microscopy and Wiesner and Mäule method. The chemical-functional group types of lignin in the stone cell of C. oleifera shell were examined by the ultraviolet spectrophotometer and transform infrared spectroscopy. The stone cells, vessels, parenchyma, and vascular tissue had existed during the young fruit growing period. The anatomical characteristics and the cell tissue ratio inverse relationship between stone cell and parenchymal cell suggested that stone cells developed from parenchymal cells. With the growth of shell, the stone cell wall thickened, and thickness-to-cavity ratio from 0 to 3.6. The fluorescent results showed that lignin content increased continuously; during shell development, the mean brightness of stone cell wall from 0 to 77.9 sections was stained with phloroglucinol-HCl, and Mäule revealed the presence of G-S-lignin in stone cells, and ImageJ results showed that G-lignin was distributed in the entire stone cell wall, while S-lignin deposition accounted for 48.59% of the cell wall area. In the FTIR spectra, the shell was identified as containing G-S-lignin.









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Boerjan W, Ralph J, Baucher M (2003) Lignin biosynthesis. Annu Rev Plant Biol 54(1):519–546. https://doi.org/10.1146/annurev.arplant.54.031902.134938
Cai Y, Li G, Nie J, Lin Y, Nie F, Zhang J, Xu Y (2010) Study of the structure and biosynthetic pathway of lignin in stone cells of pear. Sci Hortic-Amsterdam 125(3):374–379. https://doi.org/10.1016/j.scienta.2010.04.029
Chabannes M, Ruel K, Yoshinaga A, Chabbert B, Jauneau A, Joseleau J, Boudet A (2001) In situ analysis of lignins in transgenic tobacco reveals a differential impact of individual transformations on the spatial patterns of lignin deposition at the cellular and subcellular levels. Plant J 28:271–282. https://doi.org/10.1046/j.1365-313X.2001.01159.x
Chang H, Su Y, Chang S (2006) Studies on photostability of butyrylated, milled wood lignin using spectroscopic analyses. Polym Degrad Stabil 91:816–822. https://doi.org/10.1016/j.polymdegradstab
Cheng X, Li M, Li D, Zhang J, Jin Q, Sheng L, Cai Y, Lin Y (2017) Characterization and analysis of CCR and CAD gene families at the whole-genome level for lignin synthesis of stone cells in pear (Pyrus bretschneideri) fruit. Biol Open 6(11):1602–1613. https://doi.org/10.1242/bio.026997
Dong Y, Dai Y, Xu T, Cai J, Chen Q (2013) Biodegradation of chestnut shell and lignin-modifying enzymes production by the white-rot fungi Dichomitus squalens, Phlebia radiata. Bioprocess Biosyst Eng 37:755–764. https://doi.org/10.1007/s00449-013-1045-9
Engels FM, Jung HG (1998) Alfalfa stem tissues: cell-wall development and lignification. Ann Bot-London 82(5):561–568. https://doi.org/10.1006/anbo.1998.0705
Franceschi VR, Krekling T, Berryman AA, Berryman E (1998) Specialized phloem parenchyma cells in Norway Spruce (Pinaceae) bark are an important site of defense reactions. Am J Bot 85(5):601–615. https://doi.org/10.2307/2446529
Gong W, Ma Y, Lü X, Ye F, Zhao G (2017) Structural features and antioxidant activities of lignin extracted from sunflower seed shell. Food Science 38(7):23–28. https://doi.org/10.7506/spkx1002-6630-201707005
Hu J, Shi Y, Liu Y, Chang S (2018) Anatomical structure of C. oleifera shell. Protoplasma 6:1777–1784. https://doi.org/10.1007/s00709-018-1271-8
Ji Z, Ma J, Zhang Z, Xu F, Sun R (2013) Distribution of lignin and cellulose in compression wood tracheids of Pinus yunnanensis determined by fluorescence microscopy and confocal Raman microscopy. Ind Crop Prod 24:212–217. https://doi.org/10.1016/j.indcrop.2013.03.006
Jin Q, Yan C, Qiu J, Zhang N, Cai Y (2013) Structural characterization and deposition of stone cell lignin in Dangshan Su pear. Sci Hortic-Amsterdam 155:123–130. https://doi.org/10.1016/j.scienta.2013.03.020
Jones L, Ennos AR, Turner SR (2001) Cloning and characterization of irregular xylem4 (irx4): a severely lignin deficient mutant of Arabidopsis. Plant J 26:205–216. https://doi.org/10.1046/j.1365-313x.2001.01021.x
Liu Y, Hu T, Wu Z, Zeng G, Huang D, Shen Y, He X, Lai M, He Y (2014) Study on biodegradation process of lignin by FTIR and DSC. Environ Science Pollut R 21(24):14004–14013. https://doi.org/10.1007/s11356-014-3342-5
Liu C, Chen L, Tang W, Peng S, Li M, Deng N, Chen Z (2018) Predicting potential distribution and evaluating suitable soil condition of oil tea camellia in China. Forests 9:487. https://doi.org/10.3390/f9080487
López-Serrano M, Fernández María D, Pedreño MA, Ros Barceló A (2004) Zinnia elegans uses the same peroxidase isoenzyme complement for cell wall lignification in both single-cell tracheary elements and xylem vessels. J Exp Bot 55:423–431. https://doi.org/10.1093/jxb/erh036
Menden B, Kohlhoff M, Moerschbacher BM (2007) Wheat cells accumulate a syringyl-rich lignin during the hypersensitive resistance response. Phytochemistry 68(4):513–520. https://doi.org/10.1016/j.phytochem.2006.11.011
Miao Z, Yang H, Shi Z, Zheng Z, Deng J, He M (2016) Isolation and characterization of lignin fractions from hydrothermal pretreated walnut shell. Journal of Forestry Engineering 1(6):108–113. https://doi.org/10.13360/j.issn.2096-1359.2016.06.018
Moghaddam L, Rencoret J, Maliger VR, Rackemann D, Harrison MD, Gutierrez A, del Río JC, Doherty W (2017) Structural characteristics of bagasse furfural residue and its lignin component. An NMR, Py-GC/MS, and FTIR study. ACS Sustain Chem Eng 5:4846–4855. https://doi.org/10.1021/acssuschemeng.7b00274
Moya R, Berrocal A, Rodriguez-Solis M, Muñoz F (2017) Effect of steam-drying treatment on moisture content, drying rate, color and drying defects in juvenile wood of Tectona grandis from fast-growth plantations. Dry Technol 35:1832–1842. https://doi.org/10.1080/07373937.2017.1280503
Outlaw JR, William H (2003) Integration of cellular and physiological functions of guard cells. Crit Rev Plant Sci 22(6):503–529. https://doi.org/10.1080/713608316
Patten AM, Cardenas CL, Cochrane FC, Laskar DD, Bedgar DL, Davin LB, Lewis NG (2005) Reassessment of effects on lignification and vascular development in the irx4 Arabidopsis mutant. Phytochemistry 66(17):2092–2107. https://doi.org/10.1016/j.phytochem.2004.12.016
Pramod S, Rao KS, Sundberg A (2013) Structural, histochemical and chemical characterization of normal, tension and opposite wood of Subabul (Leucaena leucocephala (lam.) De wit.). Wood Sci Technol 47:777–796. https://doi.org/10.1007/s00226-013-0528-9
Reyes-Rivera J, Terrazas T (2017) Lignin analysis by HPLC and FTIR. Methods in Molecular Biology 1544:193–211. https://doi.org/10.1007/978-1-4939-6722-314
Rogers LA, Campbell MM (2004) The genetic control of lignin deposition during plant growth and development. New Phytol 164:17–30. https://doi.org/10.1111/j.1469-8137.2004.01143.x
Roussel JR, Clair B (2015) Evidence of the late lignification of the G-layer in Simarouba tension wood, to assist understanding how non-G-layer species produce tensile stress. Tree Physiol 35(12):1366–1377. https://doi.org/10.1093/treephys/tpv082
Su HM, Shih MC, Lin K (2014) Chemical composition of seed oils in native Taiwanese Camellia species. Food Chem 156:369–373. https://doi.org/10.1016/j.foodchem.2014.02.016
Sun SN, Li MF, Yuan TQ, Xu F, Sun RC (2013) Effect of ionic liquid/organic solvent pretreatment on the enzymatic hydrolysis of corncob for bioethanol production. Part 1: Structural characterization of the lignins. Ind Crops Prod 43:570–577. https://doi.org/10.1016/j.indcrop.2012.07.074
Sun FF, Tang S, Liu R, Tang Y, Wang R, Zhang Z, Gao Z, Li H, Li C, Xiao Z (2016) Biorefining fractionation of the Camellia oleifera Abel. hull into diverse bioproducts with a two-stage organosolv extraction. Ind Crops Prod 94:790–799. https://doi.org/10.1016/j.indcrop.2016.09.062
Tao S, Khanizadeh S, Zhang H (2009) Anatomy, ultrastructure and lignin distribution of stone cells in two Pyrus species. Plant Sci 176(3):413–419. https://doi.org/10.1016/j.plantsci.2008.12.011
Vanholme R, Demedts B, Morreel K, Ralph J, Boerjan W (2010) Lignin biosynthesis and structure. Plant Physiol 153(3):895–905
Wang Q, Chang S, Tan Y, Hu J (2019) Mesopore structure in C. oleifera shell. Protoplasma 256:1145–1151. https://doi.org/10.1007/s00709-019-01371-5
Whetten R, Sun YH, Zhang Y (2001) Functional genomics and cell wall biosynthesis in loblolly pine. Plant Mol Biol 47:275–291. https://doi.org/10.1023/a:1010652003395
Whitehill JG, Henderson H, Schuetz M, Skyba O, Yuen MM, King J, Al S, Mansfield SD, Bohlmann J (2015) Histology and cell wall biochemistry of stone cells in the physical defense of conifers against insects. Plant Cell and Environ 39(8):1646–1661. https://doi.org/10.1111/pce.12654
Whitehill JG, Henderson H, Strong W, Jaquish B (2016) Function of Sitka spruce stone cells as a physical defence against white pine weevil. Plant Cell and Environ 39:2545–2556. https://doi.org/10.1111/pce.12810
Xiong W, Fu JP, Wang HB, Han XD, Lei W (2007) Secondary metabolites from the fruit shells of Camellia oleifera. Chem Nat Compd 54:1189–1191. https://doi.org/10.1007/s10600-018-2592-8
Xu G, Wang L, Liu J, Wu J (2013) FTIR and XPS analysis of the changes in bamboo chemical structure decayed by white-rot and brown-rot fungi. App Surf Sci 280:799–805. https://doi.org/10.1016/j.apsusc.2013.05.065
Yoon J, Choi H, An G (2015) Roles of lignin biosynthesis and regulatory genes in plant development. J Integr Plant Biol 57:902–912. https://doi.org/10.1111/jipb.12422
Zhu J, Zhu Y, Jiang F, Ouyang J, Yu S (2013) An integrated process to produce ethanol, vanillin, and xylooligosaccharides from Camellia oleifera shell. Carbohydr Res 382:52–57. https://doi.org/10.1016/j.carres.2013.10.007
Acknowledgments
We thank Chinese National Engineering Research Center for Olitea Camellia, Changsha, People’s Republic of China, for assisting us during the field sampling.
Funding
This work was financially supported by the Hunan Provincial Natural Science Foundation of China (2020JJ2058) and the Scientific Research Project of Hunan Education Department (19A505).
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Conceived and designed the experiments: Qianqian Wang, Jinbo Hu, Shanshan Chang; performed the experiment: Qianqian Wang, Tianshu Yang; supervised the work: Jinbo Hu, Shanshan Chang; wrote the paper: Qianqian Wang, Jinbo Hu, Shanshan Chang; revised the paper: Qianqian Wang, Jinbo Hu, Shanshan Chang.
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Wang, Q., Hu, J., Yang, T. et al. Anatomy and lignin deposition of stone cell in Camellia oleifera shell during the young stage. Protoplasma 258, 361–370 (2021). https://doi.org/10.1007/s00709-020-01568-z
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DOI: https://doi.org/10.1007/s00709-020-01568-z


