|Table of Contents|

Determination of Abscisic Acid in Crabapple by High Performance Liquid Chromatography

《北方园艺》[ISSN:1001-0009/CN:23-1247/S]

Issue:
2018年04
Page:
138-144
Research Field:
Publishing date:

Info

Title:
Determination of Abscisic Acid in Crabapple by High Performance Liquid Chromatography
Author(s):
LI XiaoyingZHAO QingqingLIU YueLIU ZhenlinYANG JunmingZHANG Guojun
College of Horticulture Science & Technology,Hebei Normal University of Science & Technology,Qinhuangdao,Hebei 066600
Keywords:
crabapple (Malus sp.)high performance liquid chromatography (HPLC)abscisic acid (ABA)content
PACS:
-
DOI:
10.11937/bfyy.20172564
Abstract:
‘Strawberry jelly’ crabapple (Malus sp.) was used as test material,a reliable method for determination of abscisic acid (ABA) content in crabapple was established using the high performance liquid chromatography (HPLC) combined with solid phase extraction(SPE).By optimizing the sample pre-treatment and the chromatographic conditions,the final experimental process as follows,sample weight for 3 g,with 80% precooling methanol extracting for 12 hours,using the insoluble PVPP for adsorbing the phenolic compounds,then the extracts was decolorize by petroleum ether,and ABA was extracted by ethyl acetate,then further purification using C18 cartridge.The method was performed with a reverse-phase C18 column and using the mixture of methanol and water (containing 1.0% acetic acid) with the volume ratio of 45∶55 as mobile phase;the sample injection volume was 20 μL and the flow rate was 1.0 mL?min-1;the detection wavelength was 254 nm and the column temperature was 45 ℃.The results showed that the ABA were separated well by this method,which calibration curves had good linearity over the range from 0.01 to 0.50 μg?mL-1 with a correlation coefficient of 0.999 8,the average recovery rate for ABA was larger than 70% at three concentration levels.The abscisic acid content was lowest as 0.026 9 μg?g-1,and the highest as 0.357 9 μg?g-1 with great difference,at the concentration level of previous reported.This method showed great significance for the further research of crabapples breeding and growth.

References:

[1]王婷.天津地区观赏海棠引种与筛选[J].北方园艺,2015(3):70-72.

[2]李楠,师俊玲,王昆.14种海棠果实多酚种类及体外抗氧化活性分析[J].食品科学,2014,35(5):53-58.
[3]CHEN F,LI F,LU L,et al.Phenolic profile and changes in the antioxidant activity of crabapple(Malus domestica cv Royalty) fruit during maturation on the tree[J].International Journal of Food Science & Technology,2014,49(7):1680-1688.
[4]杨杨,范蓓,生吉萍,等.高效液相色谱法测定芒果皮中脱落酸含量[J].食品工业科技,2014(2):76-79.
[5]ARAL H,ARAL T,ZIYADANO〖AKGˇ〗ULLARI B,et al.Development of a novel amide-silica stationary phase for the reversed-phase HPLC separation of different classes of phytohormones[J].Talanta,2013,116:155-163.
[6]罗兴录,樊吴静,王军.木薯不同生育时期内源激素含量变化研究[J].中国农学通报,2011,27(21):82-86.
[7]范光宇,刘颖慧,赵治海,等.高效液相色谱法测定谷子叶尖组织中4种植物激素[J].河北农业大学学报,2015,38(1):25-28.
[8]周艳明,忻雪.高效液相色谱法测定果蔬中7种植物激素的残留量[J].食品科学,2010(18):301-304.
[9]苏齐珍,赖钟雄,叶玲娟,等.不同种类相思树试管苗内源激素的HPLC测定[J].中国农学通报,2010,26(3):216-221.
[10]KELEN M,DEMIRALAY E C,SEN S,et al.Separation of abscisic acid,indole-3-acetic acid,gibberellic acid in 99 R (Vitis berlandieri×Vitis rupestris) and rose oil (Rosa damascena Mill.) by reversed phase liquid chromatography[J].Turkish Journal of Chemistry,2004,28(5):603-610.
[11]LIU H T,LI Y F,LUAN T G,et al.Simultaneous determination of phytohormones in plant extracts using SPME and HPLC[J].Chromatographia,2007,66(7-8):515-520.
[12]陈博雯,刘海龙,陈晓明,等.高效液相色谱法分离和测定油茶茎尖组织中4种内源激素[J].山东农业科学,2012,44(3):105-107.
[13]闫师杰,郭李维,吴彩娥,等.高效液相色谱法同时测定鸭梨种子中3种内源激素[J].分析化学,2010,38(6):843-847.
[14]简利茹,李哲斐,韩青梅,等.固相萃取-HPLC测定外生菌根真菌产生植物激素IAA和GA3[J].西北农业学报,2011,20(9):165-168.
[15]QIAO J,LUO Z L,LI Y P,et al.Effect of abscisic acid on accumulation of five active components in root of Glycyrrhiza uralensis[J].Molecules,2017,22(11),doi:10.3390/molecules 22111982.
[16]胡西洲,彭西甜,余琼卫,等.固相萃取-分散液液微萃取-高效液相色谱法测定椰子汁中酸性植物激素[J].分析科学学报,2013,29(5):593-598.
[17]王水良,王平,王趁义.固相萃取-高效液相色谱法测定马尾松组织中内源激素[J].分析科学学报,2010,26(5):547-550.
[18]王璐,吴倩,段春凤,等.基质固相分散萃取-高效液相色谱-串联质谱法分析拟南芥中的赤霉素[J].色谱,2011,29(9):923-926.
[19]WANG L,DUAN C,WU D,et al.Quantification of endogenous brassinosteroids in sub-gram plant tissues by in-line matrix solid-phase dispersion-tandem solid phase extraction coupled with high performance liquid chromatography-tandem mass spectrometry[J].Journal of Chromatography A,2014,1359:44-51.
[20]DOBREV P I,HAVL〖AKCˇ〗EK L,VGNER M,et al.Purification and determination of plant hormones auxin and abscisic acid using solid phase extraction and two-dimensional high performance liquid chromatography[J].Journal of Chromatography A,2005,1075(1-2):159-166.
[21]易勇,唐旭,林锡煌,等.超高效液相色谱串联质谱法同时测定马尾藻中4种内源性植物激素[J].分析化学,2016,44(1):124-130.
[22]徐澜,高志强,安伟,等.冬麦春播小麦发育进程中主茎叶片内源激素的变化[J].核农学报,2016,30(2):355-363.
[23]周宇飞,王德权,陆樟镳,等.干旱胁迫对持绿性高粱光合特性和内源激素ABA,CTK含量的影响[J].中国农业科学,2014,47(4):655-663.
[24]张海燕,段文学,解备涛,等.不同时期干旱胁迫对甘薯内源激素的影响及其与块根产量的关系[J].作物学报,2018,44(1):126-136.
[25]丁杰,秦献军,张耀武.用高效液相色谱仪测定葡萄休眠芽的脱落酸含量[J].落叶果树,2007,39(3):4-6.
[26]赵晓菊,唐中华,郭晓瑞,等.固相萃取富集-高效液相色谱法测定长春花中的3种内源激素[J].色谱,2006,24(5):534-534.
[27]陈建华,曹阳,李昌珠,等.板栗内源激素的高效液相色谱测定方法[J].中南林业科技大学学报,2004,24(5):39-41.
[28]黄靖,刘艳芝,刘国伟,等.高效液相色谱法测定植物内源激素研究进展[J].山东农业科学,2011(8):101-103.
[29]PAN X,WELTI R,WANG X.Quantitative analysis of major plant hormones in crude plant extracts by high-performance liquid chromatography-mass spectrometry[J].Nature Protocols,2010,5(6):986-992.
[30]郭成圆,魏安智,吕平会,等.板栗雏梢分化期内源激素的动态变化特征[J].西北植物学报,2010(10):2061-2066.
[31]XU L,GAO Z Q,AN W,et al.Responses of endogenous hormone contents in leaves of main stem in different developmental stages of winter wheat varieties sowed in spring[J].Journal of Nuclear Agricultural Sciences,2016,30(2):355-363.

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Last Update: 2018-02-27