Scientia Agricultura Sinica ›› 2014, Vol. 47 ›› Issue (17): 3453-3464.doi: 10.3864/j.issn.0578-1752.2014.17.013

• HORTICULTURE • Previous Articles     Next Articles

Difference in Starch Accumulation and Characterization of Sugar Metabolism During Fruit Development of Kiwi Fruit

ZHANG Hui-qin;XIE Ming; ZHANG Chen; YANG Lu-qiong; ZHANG Zhen;XIAO Jin-ping; ZHOU Li-qiu   

  1. 1、College of Horticulture, Nanjing Agricultural University, Nanjing 210095;
    2、Institute of Horticulture, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021
  • Received:2014-03-20 Online:2014-09-01 Published:2014-05-22

Abstract: 【Objective】The aim of this work is to study difference in starch accumulation between high- and low-starch- accumulating cultivars and characterization of sugar metabolism during fruit development, and to identify the related enzymes activities in order to provide a theoretical guidance for increasing fruit sugar content and improving flavour and quality of fruit.【Method】High-starch-accumulating variety ‘Hongyang’ and low-starch-accumulating variety ‘White’ were used to measure the changes in fruit relative growth rate (RGR), carbohydrate content (starch, glucose, fructose and sucrose), dry matter and enzyme activity in relation to carbohydrate metabolism throughout the growing season.【Result】The carbohydrate concentration was negatively correlated with fruit relative growth rate, and constantly increased with starch accumulation. The starch content was positively correlated with the soluble sugar contents (glucose, fructose and sucrose) and dry matter, and the ratios of maximum starch content to carbohydrates in ‘White’ and ‘Hongyang’ fruit were 87.1% and 84.1%, respectively. The higher rate of starch accumulation, which was also maintained for a longer period of time, was found in ‘Hongyang’, and the starch peak was much higher in ‘Hongyang’ than in ‘White’. The rate of starch accumulation and the maximum starch content in ‘Hongyang’ were 0.685 mg•g-1FW•d-1 and 70.78 mg•g-1FW, and they were 1.34 and 1.69 fold higher than those in ‘White’, respectively. The period of starch accumulation of ‘Hongyang’ was 21 days longer than that of ‘White’. When starch content in ‘White’ fruit rapidly dropped, starch accumulation of ‘Hongyang’ fruit linearly increased. As a consequence, the higher level of starch concentration in ‘Hongyang’ fruit maintained until harvest, while almost all starch in ‘White’ had been converted into soluble sugars prior to harvest. Neutral invertase (NI) and acid invertase (AI) activities were consistently much higher in ‘white’ than in ‘Hongyang’. In contrast, ADP-glucose pyrophosphorylase (AGPase) and sucrose phosphate synthase (SPS) activity was always stronger in ‘Hongyang’ than in ‘White’. Fruit starch content was positively and significantly correlated with AGPase and SPS activities, but was negatively and strongly correlated with NI and AI activities. NI activity was positively and significantly correlated with NI activity, while was negatively correlated with the activities of AGPase, SPS, sucrose synthase (SS), fructokinase (FK), glucokinase (GK) and UDP-glucose pyrophosphorylase (UGPase). AGPase activity in ‘Hongyang’ had positive and significant correlation with the activities of SPS, SS, FK, GK and UGPase.【Conclusion】Kiwi fruit accumulated carbohydrate predominantly as starch. AGPase was a determinant of high starch concentration in fruit, in addition to this, the variation of NI, AI and SPS activity may be the causes of high or low contents of starch, dry matter and soluble sugars in fruit.

Key words: kiwi fruit , fruit development , starch , sugar metabolism

[1]MacRae E, Quick W P, Benker C, Stitt M. Carbohydrate metabolism during postharvest ripening in kiwifruit. Planta, 1992, 188(3): 314-323.
[2]Wegrzyn T, MacRae E. Alpha-amylase and starch degradation in kiwifruit. Journal of Plant Physiology, 1995, 147(1): 19-28.
[3]Richardson A C, Marsh K B, Boldingh, H L, Pichering A H, Bulley S M, Frearson N J, Ferguson A R, Thornber S E, Bolitho K M, MacRae E A. High growing temperatures reduce fruit carbohydrate and vitamin C in kiwifruit. Plant Cell Environ, 2004, 27(4): 423-435.
[4]Harker F R, Carr B T, Lenjo M, MacRae E A, Wismer W V, Marsh K B, Williams M, White A, Lund C M, Walker S B, Gunson F A, Pereira R B. Consumer liking for kiwifruit flavour: a meta-analysis of five studies on fruit quality. Food Quality and Preference, 2009, 20(1): 30-41.
[5]Nardozza S, Gamble J, Axten L G, Wohlers M W, Clearwater M J, Feng J, Harker F R. Dry matter content and fruit size affect flavour and texture of novel Actinidia deliciosa genotypes. Journal of the Science of Food and Agriculture, 2011, 91(4): 742-748.
[6]谢鸣, 陈学选, 高秀珍, 蒋桂华, 赵安祥. 中华猕猴桃果实主要营养成分含量在后熟过程变化的研究.园艺学报, 1991, 18(2): 173-176.
Xie M, Chen X X, Gao X Z, Jiang G H, Zhao A X. Changes in the content of the major nutrient components of fruit Actinidia chinensis during ripening. Acta Horticulturae Sinica, 1991, 18(2): 173-176. (in Chinese)
[7]常尚连, 于贤昌, 于喜艳. 西瓜果实发育过程中糖分积累与相关酶活性的变化. 西北农业学报, 2006, 15(3): 138-141.
Chang S L, Yu X C, Yu X Y. Change of sugar accumulation and related enzyme activity during fruit development of watermelon. Acta Agriculturae Boreali-occidentalis Sinica, 2006, 15(3): 138-141. (in Chinese)
[8]袁野, 吴凤芝, 周新刚.光氮互作对番茄果实糖积累及蔗糖代谢相关酶活性的影响. 中国农业科学, 2009, 42(4): 1331-1338.
Yuan Y, Wu F Z, Zhou X G. Interactive effects of light intensity and nitrogen supply on sugar accumulation and activities of enzymes related to sucrose metabolism in tomato fruits. Scientia Agricultura Sinica, 2009, 42(4): 1331-1338. (in Chinese)
[9]Lombardo V A, Osorio S, Borsani J, Lauxmann M A, Bustamante C A, Budde C O, Andreo C S, Lara M V, Fernie A R, Drincovich M F. Metabolic profiling during peach fruit development and ripening reveals the metabolic networks that underpin each developmental stage. Plant Physiology, 2011, 157(4): 1696-1710.
[10]谢鸣, 陈俊伟, 秦巧平, 蒋桂华, 孙崇波, 张慧琴, 徐红霞.转化酶和己糖激酶调控草莓聚合果内糖积累. 植物生理与分子生物学学报, 2007, 33(3): 213-218.
Xie M, Chen J W, Qin Q P, Jiang G H, Sun C B, Zhang H Q, Xu H X. The control of sugar accumulation within strawberry aggregate fruit by invertase and hexokinase. Journal of Plant Physiology and Molecular Biology, 2007, 33(3): 213-218.(in Chinese)
[11]王永章, 张大鹏. ‘红富士’苹果果实蔗糖代谢与酸性转化酶和蔗糖合酶关系的研究. 园艺学报, 2001, 28(3): 259-261.
Wang Y Z, Zhang D P. A Study on the relationships between acid invertase, sucrose synthase and sucrose metabolism in ‘Red Fuji’ apple fruit. Acta Horticulturae Sinica, 2001, 28(3): 259-261. (in Chinese)
[12]Smith G S, Clark C J, Boldingh H L. Seasonal accumulation of starch by components of the kiwifruit vine. Annals of Botany, 1992, 70(1): 19-25.
[13]Boldingh H, Smith G S, Klages K. Seasonal concentrations of non-structural carbohydrates of five Actinidia species in fruit, leaf and fine root tissue. Annals of Botany, 2000, 85(4): 469-476.
[14]Nardozza S, Boldingh H L, Richardson A C, Costa G, Marsh H, MacRae E A, Clearwater M J. Genotypic control of carbon accumulation in Actinidia deliciosa genotypes. Proceedings of the seventh international symposium on kiwifruit. Acta Horticulturae, 2011, 913: 295-301.
[15]Richardson A C, Boldingh H L, McAtee P A, Gunaseelan K, Luo Z W, Atkinson R G, David K M, Burdon J N, Schaffer R J. Fruit development of the diploid kiwifruit, Actinidia chinensis ‘Hort16A’. BMC Plant Biology, 2011, 11: 182-196.
[16]Moscatello S, Famiani F, Proietti S, Farinelli D, Battistelli A. Sucrose synthase dominates carbohydrate metabolism and relative growth rate in growing kiwifruit (Actinidia deliciosa cv. Hayward). Scientia Horticulturae, 2011, 128(3): 197-205.
[17]Wu, Y J, Xie M, Zhang Q C, Jiang G H, Zhang H Q, Long Q J, Han W J, Chen J W, Song G H. Characteristics of ‘White’: a new easy-peel cultivar of Actinidia eriantha. New Zealand Journal of Crop and Horticultural Science, 2009, 37(4): 369-373.
[18]王明忠. 红肉猕猴桃可持续育种研究. 资源开发与市场, 2003,  19(5): 309-310.
Wang M Z. Sustainable breeding research of Actinidia chinensis var. rufopulpa. Resource Development & Market, 2003, 19(5): 309-310. (in Chinese)
[19]徐昌杰, 陈文峻, 陈昆松, 张上隆. 淀粉含量测定的一种简便方法—碘显色法. 生物技术, 1998, 8(2): 41-43.
Xu C J, Chen W J, Chen K S, Zhang S L. A Simple method for determining the content of starch-Iodine Colorimety. Biotechnology, 1998, 8(2): 41-43. (in Chinese)
[20]陈俊伟, 张上隆, 张良诚, 徐昌杰, 陈昆松. 温州蜜柑果实发育进程中光合产物运输分配及糖积累特性. 植物生理学报, 2001, 27(2): 186-192.
Chen J W, Zhang S L, Zhang L C, Xu C J, Chen K S. Characteristics of photosynthetic translocation and partitioning and sugar accumulation in developing satsuma mandarin (Citrus unshiu Marc.) fruit. Acta Phytophysiologica Sinica, 2001, 27(2): 186-192. (in Chinese)
[21]Nardozza S, Boldingh H L, Osorio S, Höhne M, Wohlers M, Gleave A P, MacRae E A, Richardson A C, Atkinson R G, Sulpice R, Fernie A  R, Clearwater M J. Metabolic analysis of kiwifruit (Actinidia  deliciosa) berries from extreme genotypes reveals hallmarks for fruit starch metabolism. Journal of Experimental Botany, 2013, 64(16): 5049-5063.
[22]Guozhang Kang, Guoqin Liu, Xiaoqi Peng, Liting Wei, Chenyang Wang, YunJi Zhu,Ying Ma, Yumei Jiang, Tiancai Guo. Increasing the starch content and grain weight of common wheat by overexpression of the cytosolic AGPase large subunit gene. Plant Physiology and Biochemistry, 2013, 73(9): 93-98.
[23]Li N, Zhang S, Zhao Y, Li B, Zhang J. Over-expression of AGPase genes enhances seed weight and starch content in transgenic maize. Planta, 2011, 233(2): 241-250.
[24]Petreikov M, Shen S, Yeselson Y, Levin I, Bar M, Schaffer A. Temporally extended gene expression of the ADP-Glc pyrophosphorylase large subunit (AgpL1) leads to increased enzyme activity in developing tomato fruit. Planta, 2006, 224(6): 1465-1479.
[25]陈俊伟, 徐红霞, 谢鸣, 吴延军, 张慧琴, 冯健君. 红砂枇杷‘大红袍’与白砂枇杷‘宁海白’糖积累及代谢的差异.园艺学报, 2010, 37(6): 997-1002.
Chen J W, Xu H X, Xie M, Wu Y J, Zhang H Q, Feng J J. Difference in sugar accumulation and metabolism between red flesh and white flesh cultivar in loquat(Eriobotrya japonica Lindl.). Acta Horticulturae Sinica, 2010, 37(6): 997-1002. (in Chinese)
[26]谢鸣, 陈俊伟, 程建徽, 秦巧平, 蒋桂华, 王力宏, 王允镔, 戚行江. 杨梅果实发育与糖的积累及其关系研究. 果树学报, 2005, 22(6): 634-638.
Xie M, Chen J W, Cheng J H, Qin Q P, Jiang G H, Wang L H, Wang Y B, Qi X J. Studies on the fruit development and its relationship with sugar accumulation in bayberry fruit. Journal of Fruit Science, 2005, 22(6): 634-638. (in Chinese)
[27]杨明, 刘丽娟, 李莉云, 王博, 常金华, 刘国振. 甜高粱蔗糖积累与茎秆中SPS 表达的相关性研究. 中国农业科学, 2009, 42(1): 85-92.
Yang M, Liu L J, Li L Y, Wang B, Chang J H, Liu G Z. Correlation analysis of sugar accumulation and SPS expression in sweet sorghum (Sorghum bicolor L. Moench) stems. Scientia Agricultura Sinica, 2009, 42(1): 85-92. (in Chinese)
[28]Fung R W M, Langenkamper G, Gardner R C, MacRae E. Differential expression within an SPS gene family. Plant Science, 2003, 164(4): 459-470.
[29]Li W, Li X P, Shao Y Z, Xie J H, Chen W X, Jin Z Q. Quantification of SPS mRNA expression in banana fruit ripened under different conditions using real-time RT-PCR. Food Science Biotechnology, 2011, 20(6): 1495-1500.
[30]Dai Z W, Leon C, Feil R, Lunn J E, Delrot S, Gomes E. Metabolic profiling reveals coordinated switches in primary carbohydrate metabolism in grape berry (Vitis vinifera L.), a non-climacteric fleshy fruit. Journal of Experimental Botany, 2013, 64(5): 1345-1355.
[31]Komatsu A, Moriguchi T, Koyama K, Omura M, Akihama T. Analysis of sucrose synthase genes in citrus suggests different roles and phylogenetic relationships. Journal of Experimental Botany, 2002, 53(366): 61-71.
[32]Nguyen-Quoc B, N′Tchobo H, Foyer C H, Yelle S. Overexpression of sucrose phosphate synthase increases sucrose unloading in transformed tomato fruit. Journal of Experimental Botany, 1999, 50(335): 785-791.
[33]Woodward T J, Clearwater, M J. Relationships between ‘Hayward’ kiwifruit weight and dry matter content. Postharvest Biology Technology, 2008, 48(3): 378-382.
[34]Appeldoorn N J, Sergeeva L, Vreungdenhil D, Plas L H, Visser R G. In situ analysis of enzymes involved in sucrose to hexose-phosphate conversion during stolon-to-tuber transition of potato. Physiologia Plantarum, 2002, 115(2): 303-310.
[35]Schaffer A A, Petreikov M. Sucrose metabolism in young tomato fruit undergoing transient sucrose to starch metabolism. Plant Physiology, 1997, 113(3): 739-746.
[1] ZHANG JiaHua,YANG HengShan,ZHANG YuQin,LI CongFeng,ZHANG RuiFu,TAI JiCheng,ZHOU YangChen. Effects of Different Drip Irrigation Modes on Starch Accumulation and Activities of Starch Synthesis-Related Enzyme of Spring Maize Grain in Northeast China [J]. Scientia Agricultura Sinica, 2022, 55(7): 1332-1345.
[2] LI ShiJia,LÜ ZiJing,ZHAO Jin. Identification of R2R3-MYB Subfamily in Chinese Jujube and Their Expression Pattern During the Fruit Development [J]. Scientia Agricultura Sinica, 2022, 55(6): 1199-1212.
[3] XIAO LuTing,LI XiuHong,LIU LiJun,YE FaYin,ZHAO GuoHua. Effects of Starch Granule Size on the Physical and Chemical Properties of Barley Starches [J]. Scientia Agricultura Sinica, 2022, 55(5): 1010-1024.
[4] JIANG JingJing,ZHOU TianYang,WEI ChenHua,WU JiaNing,ZHANG Hao,LIU LiJun,WANG ZhiQin,GU JunFei,YANG JianChang. Effects of Crop Management Practices on Grain Quality of Superior and Inferior Spikelets of Super Rice [J]. Scientia Agricultura Sinica, 2022, 55(5): 874-889.
[5] YOU JiaLing,LI YouMei,SUN MengHao,XIE ZhaoSen. Analysis Reveals the Differential Expression of Genes Related to Starch Accumulation in Chloroplast of Leaf with Different Ages in Pinot Noir Grape [J]. Scientia Agricultura Sinica, 2022, 55(21): 4265-4278.
[6] CUI Peng,ZHAO YiRen,YAO ZhiPeng,PANG LinJiang,LU GuoQuan. Starch Physicochemical Properties and Expression Levels of Anabolism Key Genes in Sweetpotato Under Low Temperature [J]. Scientia Agricultura Sinica, 2022, 55(19): 3831-3840.
[7] FANG HanMo,HU ZhangJian,MA QiaoMei,DING ShuTing,WANG Ping,WANG AnRan,SHI Kai. Function of SlβCA3 in Plant Defense Against Pseudomonas syringae pv. tomato DC3000 [J]. Scientia Agricultura Sinica, 2022, 55(14): 2740-2751.
[8] JIN MengJiao,LIU Bo,WANG KangKang,ZHANG GuangZhong,QIAN WanQiang,WAN FangHao. Light Energy Utilization and Response of Chlorophyll Synthesis Under Different Light Intensities in Mikania micrantha [J]. Scientia Agricultura Sinica, 2022, 55(12): 2347-2359.
[9] WANG LiJian,LUO Cheng,PAN XueFeng,CHEN Xia,CHEN YinJi. Effects of Cellulose Replacing Starch on the Gel Properties of Myofibrillar Protein [J]. Scientia Agricultura Sinica, 2022, 55(11): 2227-2238.
[10] XuXian XUAN,ZiLu SHENG,ZhenQiang XIE,YuQing HUANG,PeiJie GONG,Chuan ZHANG,Ting ZHENG,Chen WANG,JingGui FANG. Function Analysis of vvi-miR172s and Their Target Genes Response to Gibberellin Regulation of Grape Berry Development [J]. Scientia Agricultura Sinica, 2021, 54(6): 1199-1217.
[11] NIU HongZhuang,LIU Yang,LI XiaoPing,HAN YuXuan,WANG KeKe,YANG Yan,YANG QianHui,MIN DongHong. Effects of Physicochemical Properties of Wheat (Triticum aestivum L.) Starch with Different HMW-GSs Combinations on Dough Stability [J]. Scientia Agricultura Sinica, 2021, 54(23): 4943-4953.
[12] WANG YuLin,LEI Lin,XIONG WenWen,YE FaYin,ZHAO GuoHua. Effects of Steaming-Retrogradation Pretreatment on Physicochemical Properties and in Vitro Starch Digestibility of the Roasted Highland Barley Flour [J]. Scientia Agricultura Sinica, 2021, 54(19): 4207-4217.
[13] GU MingHui,LIU YongFeng,SHEN Qian,QIAO ChunYan. Improving Quality and Delaying Oxidation in Goat Meat Refrigeration by Polyphenols from Thinned Young Kiwifruit [J]. Scientia Agricultura Sinica, 2020, 53(8): 1643-1654.
[14] ZOU JianQiu. New Research Progress on Sorghum Breeding and Cultivation Techniques [J]. Scientia Agricultura Sinica, 2020, 53(14): 2769-2773.
[15] KE FuLai,ZHU Kai,LI ZhiHua,SHI YongShun,ZOU JianQiu,WANG YanQiu. Formation Regulating and Micro-Structure of Sorghum Starch with Different Types of Endosperm [J]. Scientia Agricultura Sinica, 2020, 53(14): 2774-2785.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!