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Abstract
Since the carbohydrate content affects pear flavor during the process of growth, it is necessary to determine the sugar components that accumulate in the fruit. We analyzed the fruit carbohydrate content, and the gene expression and activity of acid invertase (AI), neutral invertase (NI), sucrose synthase (SS), and sucrose phosphate synthase (SPS) during the development of “Huangguan” and “Yali” pears. The results demonstrate that during development, the fruit sugar metabolism of the “Huangguan” pear follows a typical sorbitol–starch-soluble sugars middle model, whereas the “Yali” pear fruit follows a typical sorbitol–sucrose–starch-soluble sugars middle model. In the “Huangguan” pear, we found the AI and NI gene expressions, as well as AI (P < 0.05) and NI (P < 0.01) enzyme activities, to be positively correlated, whereas we found the NI gene expression and NI enzyme activity of “Yali” pear to be negatively correlated (P < 0.01). We observed the high levels of late-stage AI and early-stage SS during development to roughly correspond with the gene expression found in the late and early stages, respectively, suggesting their potential regulatory roles in “Huangguan” pear fruit development. Our results indicate that the primary function of SPS during the early developmental stage is to accumulate sucrose, whereas the primary function of AI is to promote hexose accumulation during the late developmental stage of mature “Yali” pear fruit.
Keywords
“Huangguan” pear
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“Yali” pear
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Sugar metabolism
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Enzyme activity
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Gene expression
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Xiaohong Kou, Yunfei Li, Ying Zhang, Bianling Jiang, Zhaohui Xue.
Gene Expression and Activity of Enzymes Involved in Sugar Metabolism and Accumulation During “Huangguan” and “Yali” Pear Fruit Development.
Transactions of Tianjin University, 2018, 24(2): 101-110 DOI:10.1007/s12209-017-0104-8
| [1] |
Yu LN, Liu HX, Shao XF, et al. Effects of hot air and methyl jasmonate treatment on the metabolism of soluble sugars in peach fruit during cold storage. Postharvest Biol Technol, 2016, 113: 8-16.
|
| [2] |
Hu LS, Wu G, Hao CY, et al. Transcriptome and selected metabolite analyses reveal points of sugar metabolism in jackfruit (Artocarpus heterophyllus Lam.). Plant Sci, 2016, 248: 45-56.
|
| [3] |
Yang ZY, Wang TD, Wang HC, et al. Patterns of enzyme activities and gene expressions in sucrose metabolism in relation to sugar accumulation and composition in the aril of Litchi chinensis Sonn. J Plant Physiol, 2013, 170(8): 731-740.
|
| [4] |
Jiang N, Jin LF, da Silva JAT, et al. Activities of enzymes directly related with sucrose and citric acid metabolism in citrus fruit in response to soil plastic film mulch. Sci Hortic, 2014, 168(3): 73-80.
|
| [5] |
Basson CE, Groenewald JH, Kossmann J, et al. Sugar and acid-related quality attributes and enzyme activities in strawberry fruits: invertase is the main sucrose hydrolysing enzyme. Food Chem, 2010, 121(4): 1156-1162.
|
| [6] |
Choudhury SR, Roy S, Sengupta DN. A comparative study of cultivar differences in sucrose phosphate synthase gene expression and sucrose formation during banana fruit ripening. Postharvest Biol Technol, 2009, 54(1): 15-24.
|
| [7] |
Roitsch T, Gonzalez MC. Function and regulation of plant invertases: sweet sensations. Trends Plant Sci, 2004, 9(12): 606-613.
|
| [8] |
Manning K, Maw GA. Distribution of acid invertase in the tomato plant. Phytochemistry, 1975, 14(9): 1965-1969.
|
| [9] |
Moscatello S, Famiani F, Proietti S, et al. Sucrose synthase dominates carbohydrate metabolism and relative growth rate in growing kiwifruit (Actinidia deliciosa, cv Hayward). Sci Hortic, 2011, 128(3): 197-205.
|
| [10] |
Bosch S, Grof CPL, Botha F. Expression of neutral invertase in sugarcane. Plant Sci, 2004, 166(5): 1125-1133.
|
| [11] |
Ruan YL, Jin Y, Yang YJ, et al. Sugar input, metabolism, and signaling mediated by invertase: roles in development, yield potential, and response to drought and heat. Mol Plant, 2010, 3(6): 942-955.
|
| [12] |
Tanase K, Yamaki S. Sucrose synthase isozymes related to sucrose accumulation during fruit development of Japanese pear (Pyrus pyrifolia Nakai). J Jpn Soc Hortic Sci, 2000, 69(6): 671-676.
|
| [13] |
Lopez-Gomez R, Gomez-Lim MA. A method for extracting intact RNA from fruits rich in polysaccharides using ripe mango mesocarp. HortScience, 1992, 27(5): 440-442.
|
| [14] |
Nielsen TH, Skjærbæ HC, Karlsen P. Carbohydrate metabolism during fruit development in sweet pepper (Capsicum annuum) plants. Physiol Plantarum, 1991, 82(2): 311-319.
|
| [15] |
Mbéguié-A-Mbéguié D, Fils-Lycaon B, Chillet M. Extraction and purification of total RNA from banana tissues (small scale). Fruits, 2008, 63(4): 255-262.
|
| [16] |
Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method. Methods, 2001, 25(4): 402-408.
|
| [17] |
Fils-Lycaon B, Julianus P, Chillet M. Acid invertase as a serious candidate to control the balance sucrose versus (glucose plus fructose) of banana fruit during ripening. Sci Hortic, 2011, 129(2): 197-206.
|
| [18] |
Moriguchi T, Abe K, Sanada T, et al. Levels and role of sucrose synthase, sucrose-phosphate synthase, and acid invertase in sucrose accumulation in fruit of Asian pear. J Am Soc Hortic Sci, 1992, 117(2): 274-278.
|
| [19] |
Chen JL, Wang ZF, Wu JH, et al. Chemical compositional characterization of eight pear cultivars grown in China. Food Chem, 2007, 104(1): 268-275.
|
| [20] |
Zheng GQ, Zheng ZY, Xu X, et al. Variation in fruit sugar composition of Lycium barbarum L. and Lycium chinense Mill. of different regions and varieties. Biochem Syst Ecol, 2010, 38(3): 275-284.
|
| [21] |
Nitsch J. The physiology of fruit growth. Annu Rev Plant Physiol, 1953, 4(4): 199-236.
|
| [22] |
Mwaniki MW, Mathooko FM, Matsuzaki M, et al. Expression characteristics of seven members of the beta-galactosidase gene family in ‘La France’ pear (Pyrus communis L.) fruit during growth and their regulation by 1-methylcyclopropene during postharvest ripening. Postharvest Biol Technol, 2005, 36(3): 25-263.
|
| [23] |
Beruter J. Carbohydrate metabolism in two apple genotypes that differ in malate accumulation. J Plant Physiol, 2004, 161(9): 1011-1029.
|
| [24] |
Klann EM, Chetelat RT, Bennett AB. Expression of acid invertase gene controls sugar composition in tomato (Lycopersicon) fruit. Plant Physiol, 1993, 103(3): 863-870.
|
| [25] |
Miron D, Schaffer AA. Sucrose phosphate synthase, sucrose synthase and acid invertase activities in developing tomato fruit of Lycopersicon esculentum Mill. and the sucrose accumulating Lycopersicon hirsutum Humb. and Bonpl. Plant Physiol, 1991, 95(2): 623-627.
|
| [26] |
Giorno F, Guerriero G, Biagetti M, et al. Gene expression and biochemical changes of carbohydrate metabolism in in vitro micro-propagated apple plantlets infected by ‘Candidatus Phytoplasma mali’. Plant Physiol Biochem, 2013, 70: 311-317.
|
| [27] |
Kajiura I, Yamaki S, Omura M, et al. Improvement of sugar content and composition in fruits, and classifications of East Asian pears by the principal component analysis of sugar compositions in fruits. Jpn J Breed, 1979, 29(1): 1-12.
|
| [28] |
Wang L, Cui N, Zhao XC, et al. Accumulation of carbohydrate and regulation of 14-3-3 protein on sucrose phosphate synthase (SPS) activity in two tomato species. J Integr Agric, 2014, 13(2): 358-364.
|
| [29] |
Sturm A, Tang GQ. The sucrose-cleaving enzymes of plants are crucial for development, growth and carbon partitioning. Trends Plant Sci, 1999, 4(10): 401-407.
|
| [30] |
Yelle S, Chetelat RT, Dorais M, et al. Sink metabolism in tomato fruit: IV. Genetic and biochemical analysis of sucrose assimilation. Plant Physiol, 1991, 95(4): 1026-1035.
|
| [31] |
Sun JD, Loboda T, Sung SJS, et al. Sucrose synthase in wild tomato, Lycopersicon chmielewskii, and tomato fruit sink strength. Plant Physiol, 1992, 98(3): 1163-1169.
|