Deactivating mutations in the catalytic site of a companion serine carboxypeptidase-like acyltransferase enhance catechin galloylation in Camellia plants

Xiangxiang Chen , Xue Zhang , Yue Zhao , Liping Gao , Zhihui Wang , Yanlei Su , Lingyun Zhang , Tao Xia , Yajun Liu

Horticulture Research ›› 2025, Vol. 12 ›› Issue (3) : 343

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Horticulture Research ›› 2025, Vol. 12 ›› Issue (3) : 343 DOI: 10.1093/hr/uhae343
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Deactivating mutations in the catalytic site of a companion serine carboxypeptidase-like acyltransferase enhance catechin galloylation in Camellia plants

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Abstract

Galloylated flavan-3-ols are key quality and health-related compounds in tea plants of Camellia section Thea. Camellia ptilophylla and Camellia sinensis are two representative species known for their high levels of galloylated flavan-3-ols. Building on our knowledge of galloyl catechin biosynthesis in C. sinensis, we now focus on the biosynthesis of galloylated phenolics in C. ptilophylla, aiming to elucidate the mechanisms underlying the high accumulation of these compounds in Camellia species. The phenolic compounds in C. ptilophylla were identified and quantified using chromatographic and colorimetric methods. Genes involved in polyphenol galloylation were identified by correlating gene expression with the accumulation of galloylated phenolics across 18 additional Camellia species and one related species using Weighted Gene Coexpression Network Analysis. Key findings include the coexpression of SCPL4/2 and SCPL5 subgroup enzymes as crucial for galloylation of catechins, while SCPL3 and SCPL8 showed enzymatic activity related to hydrolyzable tannin synthesis. Variations in the amino acid sequences of SCPL5, particularly in the catalytic triad (T-D-Y vs S-D-H) observed in C. ptilophylla and C. sinensis, were found to significantly affect enzymatic activity and epigallocatechin gallate (EGCG) production. In conclusion, this research provides important insights into the metabolic pathways of C. ptilophylla, emphasizing the critical role of SCPL enzymes in shaping the phenolic profile within the section Thea. The findings have significant implications for the cultivation and breeding of tea plants with optimized phenolic characteristics.

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Xiangxiang Chen, Xue Zhang, Yue Zhao, Liping Gao, Zhihui Wang, Yanlei Su, Lingyun Zhang, Tao Xia, Yajun Liu. Deactivating mutations in the catalytic site of a companion serine carboxypeptidase-like acyltransferase enhance catechin galloylation in Camellia plants. Horticulture Research, 2025, 12(3): 343 DOI:10.1093/hr/uhae343

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Acknowledgements

This work was financially supported by the National Key Research and Development Program of China (2022YFF1003103), Anhui Provincial Natural Science Foundation (2308085MC94, 202204c06020035), and the joint funds of National Natural Science Foundation of China (U21A20232).

Author contributions

Y.L., L.G., and T.X. conceived and designed the experiments. X.C., Y.Z., X.Z., and Y.S. conducted the experiments and performed data analysis. Z.W. contributed to enzyme activity assays. L.Z. was responsible for plant material preparation. X.C. and Y.L. drafted the manuscript. All authors reviewed and approved the final manuscript.

Data availability

All data generated from the study appear in the submitted article.

Conflict of interest statement

The authors declare no competing interests.

Supplementary data

Supplementary data is available at Horticulture Research online.

References

[1]

St M, Milkowski C. Serine carboxypeptidase-like acyltrans-ferases from plants. Methods Enzymol. 2012;516: 279-97

[2]

Gomez C, Terrier N, Torregrosa L. et al. Grapevine MATE-type proteins act as vacuolar H+-dependent acylated anthocyanin transporters. Plant Physiol. 2009;150: 402-15

[3]

Zhao J, Dixon RA. The ’ins’ and ’outs’ of flavonoid transport. Trends Plant Sci. 2010;15: 72-80

[4]

Ciarkowska A, Ostrowski M, Starzynska E. et al. Plant SCPL acyltransferases: multiplicity of enzymes with various functions in secondary metabolism. Phytochem Rev. 2019;18: 303-16

[5]

Bontpart T, Cheynier V, Ageorges A. et al. BAHD or SCPL acyl-transferase? What a dilemma for acylation in the world of plant phenolic compounds. New Phytol. 2015;208: 695-707

[6]

Fu R, Zhang P, Jin G. et al. Versatility in acyltransferase activity completes chicoric acid biosynthesis in purple coneflower. Nat Commun. 2021;12:1563

[7]

Li AX, Eannetta N, Ghangas GS. et al. Glucose polyester biosyn-thesis. Purification and characterization of a glucose acyltrans-ferase. Plant Physiol. 1999;121: 453-60

[8]

Mugford ST, Qi X, Bakht S. et al. A serine carboxypeptidase-like acyltransferase is required for synthesis of antimicrobial compounds and disease resistance in oats. Plant Cell. 2009;21: 2473-84

[9]

Takashi A, Yasuhiko S, Ayako I. et al. Condensed tannin composi-tion analysis in persimmon (Diospyros kaki Thunb.) fruit by acid catalysis in the presence of excess phloroglucinol. J Jpn Soc Hortic Sci. 2010;79: 275-81

[10]

Obreque-Slier E, Pena-Neira A, Lopez-Solis R. et al. Comparative study of the phenolic composition of seeds and skins from carmenere and cabernet sauvignon grape varieties (Vitis vinifera L.) during ripening. J Agric Food Chem. 2010;58: 3591-9

[11]

Jiang X, Liu Y, Li W. et al. Tissue-specific, development-dependent phenolic compounds accumulation profile and gene expression pattern in tea plant [Camellia sinensis]. PLoS One. 2013;8:e62315

[12]

Chang Y, Gong W, Xu J. et al. Integration of semi-in vivo assays and multi-omics data reveals the effect of galloylated catechins on self-pollen tube inhibition in Camellia oleifera. Hortic Res. 2023;10:uhac248

[13]

Singh NA, Mandal AK, Khan ZA. Potential neuroprotective prop-erties of epigallocatechin-3-gallate (EGCG). Nutr J. 2016;15:60

[14]

Legeay S, Rodier M, Fillon L. et al. Epigallocatechin gallate: a review of its beneficial properties to prevent metabolic syn-drome. Nutrients. 2015;7: 5443-68

[15]

Chang HD, Ren SX. FloraofChina. Vol. 49. Bejing, China: Science Press; 1998:115-37

[16]

Ming TL. Flora of China (English Version). Beijing, China: Science and Technology Press; 2000:

[17]

Xia EH, Zhang HB, Sheng J. et al. The tea tree genome provides insights into tea flavor and independent evolution of caffeine biosynthesis. Mol Plant. 2017;10: 866-77

[18]

Yang XR, Ye CX, Xu JK. et al. Simultaneous analysis of purine alkaloids and catechins in Camellia sinensis, Camellia ptilophylla and Camellia assamica var. kucha by HPLC. Food Chem. 2007;100: 1132-6

[19]

Jin JQ, Chai YF, Liu YF. et al. Hongyacha, a naturally caffeine-free tea plant from Fujian. China J Agric Food Chem. 2018;66: 11311-9

[20]

Zhao Y, Yao S, Zhang X. et al. Flavan-3-ol galloylation-related functional gene cluster and the functional diversification of SCPL paralogs in Camellia sp. J Agric Food Chem. 2023;71: 488-98

[21]

Wang Z, Chen X, Zhao Y. et al. A serine carboxypeptidase-like acyltransferase catalyzes consecutive four-step reactions of hydrolyzable tannin biosynthesis in Camellia oleifera. Plant J. 2024;119: 1299-312

[22]

Zhuang JH, Dai XL, Zhu MQ. et al. Evaluation of astringent taste of green tea through mass spectrometry-based targeted metabolic profiling of polyphenols. Food Chem. 2020;305:125507

[23]

Yao SB, Liu YJ, Zhuang JH. et al. Insights into acylation mecha-nisms: co-expression of serine carboxypeptidase-like acyltrans-ferases and their non-catalytic companion paralogs. Plant J. 2022;111: 117-33

[24]

Hall TA. BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser. 1999;41: 95-8

[25]

Tang J, Li R, Wu B. et al. Secondary metabolites with antioxidant and antimicrobial activities from Camellia fascicularis. Curr Issues Mol Biol. 2024;46: 6769-82

[26]

Linh NN, Huong NTM, Dai DN. et al. Camellia annamensis (Theaceae): phytochemical analysis, cytotoxic, antioxidative, and antimicrobial activities. Nat Prod Res. 2024;1-7

[27]

Pereira AG, Garcia-Perez P, Cassani L. et al. Camellia japonica:a phytochemical perspective and current applications facing its industrial exploitation. Food Chem X. 2022;13:100258

[28]

Gao DF, Xu M, Yang CR. et al. Phenolic antioxidants from the leaves of Camellia pachyandra Hu. J Agric Food Chem. 2010;58: 8820-4

[29]

Ming TL. A revision of Camellia section. Thea. Acta Bot Yunnan. 1992;14: 115-32

[30]

Meng XH, Li N, Zhu HT. et al. Plant resources, chemical con-stituents, and bioactivities of tea plants from the genus Camellia section Thea. J Agr Food Chem. 2019;67: 5318-49

[31]

Han Z, Wen M, Zhang H. et al. LC-MS based metabolomics and sensory evaluation reveal the critical compounds of dif-ferent grades of Huangshan Maofeng green tea. Food Chem. 2022;374:131796

[32]

Wang XC. Tea Biochemistry. Bejing, China: China Agriculture Press; 2003:

[33]

Ying C, Chen J, Chen J. et al. Differential accumulation mecha-nisms of purine alkaloids and catechins in Camellia ptilophylla,a natural theobromine-rich tea. Beverage Plant Res. 2023;3:15

[34]

Xia E, Tong W, Hou Y. et al. The reference genome of tea plant and resequencing of 81 diverse accessions provide insights into its genome evolution and adaptation. Mol Plant. 2020;13: 1013-26

[35]

Gao Q, Tong W, Li F. et al. TPIA2: an updated tea plant infor-mation archive for Camellia genomics. Nucleic Acids Res. 2024;52: D1661-7

[36]

Chen Y, Jiang C, Yin S. et al. New insights into the function of plant tannase with promiscuous acyltransferase activity. Plant J. 2023;113: 576-94

[37]

Li Z, De La Torre AR, Sterck L. et al. Single-copy genes as molecu-lar markers for phylogenomic studies in seed plants. Genome Biol Evol. 2017;9: 1130-47

[38]

Stamatakis A. RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics. 2014;30: 1312-3

[39]

Posada D. ModelTest Server: a web-based tool for the statistical selection of models of nucleotide substitution online. Nucleic Acids Res. 2006;34: W700-3

[40]

Kumar S, Stecher G, Tamura K. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol. 2016;33: 1870-4

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