Integrated metabolomic and transcriptomic analyses provide comprehensive new insights into the mechanism of chitosan delay of kiwifruit postharvest ripening

被引:10
|
作者
Yang, Haiying [1 ,2 ]
Zhang, Xueli [1 ]
Wu, Rui [1 ]
Tang, Xiaoli [3 ]
Yang, Yanqing [1 ]
Fan, Xinguang [1 ]
Gong, Hansheng [1 ]
Grierson, Donald [4 ]
Yin, Xueren [5 ]
Li, Jianzhao [3 ]
Zhang, Aidi [1 ]
机构
[1] Ludong Univ, Yantai Engn Res Ctr Food Green Proc & Qual Control, Sch Food Engn, Yantai Key Lab Nanosci & Technol Prepared Food, Yantai 264025, Peoples R China
[2] Hunan Agr Univ, Coll Food Sci & Technol, Changsha 410125, Peoples R China
[3] Ludong Univ, Engn Res Inst Agr & Forestry, Yantai 264025, Peoples R China
[4] Univ Nottingham, Sch Biosci, Plant & Crop Sci Div, Sutton Bonington Campus, Loughborough LE125RD, England
[5] Anhui Agr Univ, Sch Hort, Hefei 230036, Peoples R China
基金
中国国家自然科学基金;
关键词
Kiwifruit; Chitosan; Fruit ripening; Transcriptome; Metabolome; CELL-WALL METABOLISM; ACTINIDIA-CHINENSIS; FRUIT; ETHYLENE; IDENTIFICATION; COATINGS; STARCH; PEACH; ACID;
D O I
10.1016/j.postharvbio.2023.112746
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Chitosan (CTS) plays an important role in delaying fruit ripening and extending fruit shelf life when used as an eco-friendly and edible coating. However, there is still limited understanding about the molecular mechanisms and effects of chitosan on the quality of postharvest kiwifruit. In this study, firmness, total soluble solid, acid, phenolic content, flavonoid content, starch and ascorbic acid concentration, ethylene production, and cell-wall components were determined after CTS treatment. Fruit treated with CTS maintained higher firmness, starch and flavonoids (3.85-, 1.78-and 2.08-fold higher, respectively, after 6d compared to the control). Widely targeted metabolome analysis revealed flavonoids (dihydrokaempferol-7-O-glucoside, eriodictyol-3 '-O-glucoside) and lipids (LysoPC 16:0 (2 n isomer)), and punicic acid (9Z,11E,13Z-octadecatrienoic acid) were the main differential metabolites. KEGG pathway enrichment analysis showed 'metabolic pathways (ko01100)' and 'biosynthesis of secondary metabolites (ko01110)' were the main KEGG pathways. Integrated metabolomic and transcriptomic analyses revealed that the expression of five key structural genes, including three starch degradation genes (AcBAM3L, AcBAM3.1, Acc31818 (PHS)), one cell-wall modification gene (AcPG1), and one flavonoids biosynthesis gene (Acc18331 (F3'H)), and 12 transcription factors (AcNAC083, AcRAP2-10, AcERF14, AcERF64, Acc27131 (bZIP), AcHSFB2a, Acc12589 (IAA), AcMYB13, Acc20159 (bHLH), AcBEL1, AcbHLH149, AcWRKY75) were different. Real-time PCR analyses verified that the expression of AcBAM3L, AcBAM3.1, AcPG1 and most of the 12 transcription factors were suppressed by CTS treatment, while the expression of Acc31818 (PHS), Acc18331 (F3'H) and AcBEL1 were enhanced by CTS treatment. Together, these CTS-responsive genes may play critical roles in determining the rate of ripening and quality change of postharvest kiwifruit.
引用
收藏
页数:12
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