|Table of Contents|

Growth,Physiology and Biochemistry Responses of Pueraria lobata to Low Temperature Stress

《北方园艺》[ISSN:1001-0009/CN:23-1247/S]

Issue:
2022年18
Page:
109-116
Research Field:
Publishing date:

Info

Title:
Growth,Physiology and Biochemistry Responses of Pueraria lobata to Low Temperature Stress
Author(s):
ZENG HongxueQU Xinghong
(Zhejiang Tongji Vocational College of Science and Technology,Hangzhou,Zhejiang 311231)
Keywords:
Pueraria lobatalow temperature stressgrowthphysiological and biochemical
PACS:
-
DOI:
10.11937/bfyy.20220955
Abstract:
Taking Hunan and Australian Pueraria lobata germplasms as experimental materials,the growth,physiological and biochemical changes and low temperature tolerance of two Pueraria lobata germplasms under artificial simulated temperature gradients of 25 ℃,15 ℃ and 10 ℃ were studied and analyzed by using the method of low temperature gradient test,in order to provide reference for the utilization of Pueraria lobata.The results showed that the growth indexes (growth rate,fresh weight,dry weight,leaf area,leaf width,leaf length and leaf perimeter) of the two Pueraria lobata germplasms decreased with the decrease of temperature.Conductivity,malondialdehyde content,osmotic adjustment substance content (soluble sugar,proline),antioxidant enzyme activity (catalyst,peroxidase,superoxide dismutase,ascorbate peroxidase) all increased with the decrease of temperature.The contents of ABA increased,while the contents of GA3,IAA and ZT decreased with the decrease of temperature.Under low temperature conditions,the growth indicators,osmotic adjustment material content,antioxidant enzyme activity and endogenous hormone content of Australian germplasm were basically higher than those of Hunan germplasm.In conclusion,the two Pueraria lobata germplasms adapt to low temperature stress by slowing down the growth rate of plants,reducing biomass,changing leaf morphological parameters,reducing the content of endogenous hormones,improving osmotic adjustment substances and increasing the activity of antioxidant enzymes.Under low temperature stress,the accumulation or maintenance of higher osmotic adjustment material content,antioxidant enzyme activity and endogenous hormone content may be the main reason why Australian germplasm has stronger cold tolerance than Hunan germplasm.

References:

[1]吴德邻.中国葛属(Pueraria DC.)的研究[J].热带亚热带植物学报,1994(3):12-21.[2]丁艳芳.葛藤的价值及其开发前景[J].西北林学院学报,2003(3):86-89.[3]陈俊,冯成进,杨义成.葛藤是石漠化治理的优秀先锋植物[J].现代园艺,2014(14):3.[4]朱邦长,叶玛丽.贵州天然豆科牧草:窄叶野豌豆的引种与驯化[J].草业科学,1996,13(4):4.[5]朱五星.大别山区具有开发前途的饲用植物:葛藤[J].中国草地,1996(6):1.[6]王家玉.葛藤的经济价值和开发利用[J].生物学通报,1998(6):46-47.[7]VELIKOVA V,YORDANOV I,EDREVA A.Oxidative stress and some antioxidant systems in acid rain-treated bean plants[J].Plant Science,2000,151(1):59-66.[8]UEMURA M,WARREN G,STEPONKUS P L.Freezing sensitivity in the sfr4 mutant of Arabidopsis is due to low sugar content and is manifested by loss of osmotic responsiveness[J].Plant Physiology,2003,131(4):1800-1807.[9]LI S,YONG Y,ZHANG Q,et al.Differential physiological and metabolic response to low temperature in two zoysiagrass genotypes native to high and low latitude[J].PLoS One,2018,13(6):e0198885.[10]ZHANG T,MO J,ZHOU K,et al.Overexpression of Brassica campestris BcICE1 gene increases abiotic stress tolerance in tobacco[J].Plant Physiology & Biochemistry,2018,132:515-523.[11]SHARMA R,SINGH G,BHATTACHARYA S,et al.Comparative transcriptome meta-analysis of Arabidopsis thaliana under drought and cold stress[J].PLoS One,2018,13(9):e0203266.〖JP〗[12]田丰,于闯,付双军,等.7份红豆草对低温的生理响应及抗寒性评价[J].甘肃农业科技,2018,514(10):25-30.[13]王萍,李彦慧,张雪梅,等.低温对仁用杏雌蕊抗坏血酸-谷胱甘肽循环的影响[J].园艺学报,2013,40(3):9.[14]杨勇,娄燕宏,杨知建,等.低温胁迫对狗牙根激素和碳水化合物代谢的影响[J].草业学报,2016,25(2):205-215.[15]郭建平,孙其荣,周全.葛根药理作用研究进展[J].中草药,1995(3):163-165.[16]张倩.野葛根饲喂奶牛的适宜性评价[D].郑州:郑州大学,2011.[17]谭景晨,赵丽丽,张淑炜,等.干旱胁迫对葛藤种子萌发的影响[J].农技服务,2021,38(1):4.[18]郭树勋,杨然,胡晓辉,等.低温和亚低温对番茄幼苗生长及生理特性的影响[J].山西农业科学,2021,49(9):5.[19]李丽杰,顾万荣,李从锋,等.DCPTA对低温下玉米叶片抗氧化系统及渗透调节物质的影响[J].植物生理学报,2016,52(12):13.[20]FERNNDEZ D-S N,IGOR F-SJOS C-M M,et al.Salinity tolerance is related to cyanide-resistant alternative respiration in Medicago truncatula under sudden severe stress[J].Plant,Cell & Environment,2016,39(11):2361-2369.[21]丁红映,王明,谢洁,等.植物低温胁迫响应及研究方法进展[J].江苏农业科学,2019,47(14):6.[22]岳俊芹,张素瑜,李向东,等.低温胁迫对小麦叶绿素荧光参数及产量的响应[J].麦类作物学报,2021,41(1):105-110.[23]赵孟良,郭怡婷,孙世英,等.低温胁迫下4种菊芋的耐寒性评价[J].植物生理学报,2020(7):13.[24]简令成.生物膜与植物寒害和抗寒性的关系[J].植物学报,1983(1):17-23.[25]杨勇,娄燕宏,杨知建,等.低温胁迫对狗牙根激素和碳水化合物代谢的影响[J].草业学报,2016(2):205-215.[26]艾琳,张萍,胡成志.低温胁迫对葡萄根系膜系统和可溶性糖及脯氨酸含量的影响[J].新疆农业大学学报,2004(4):47-50.[27]李轶冰,杨顺强,任广鑫,等.低温处理下不同禾本科牧草的生理变化及其抗寒性比较[J].生态学报 2009,29(3):1341-1347.[28]何子华,杨成行,王沛,等.高寒地区6种禾本科牧草对低温胁迫的生理响应及耐寒性评价[J].草业科学,2021,38(10):2019-2028.[29]GAO S S,WANG Y L,YU S,et al.Effects of drought stress on growth,physiology and secondary metabolites of two Adonis species in Northeast China[J].Scientia Horticulturae,2020,259:1-10.[30]赵娜,徐庆国,苏鹏,等.7个暖季型草坪草品种对低温胁迫的抗性差异研究[J].草地学报,2020,28(2):375-382.[31]许树成,丁海东,鲁锐,等.ABA在植物细胞抗氧化防护过程中的作用[J].中国农业大学学报,2008,13(2):11-19.[32]黄杏.外源ABA提高甘蔗抗寒性的生理及分子机制研究[D].南宁:广西大学,2012.[33]孙宗玖,李培英,阿不来提,等.外源脱落酸对抗寒性狗牙根抗氧化酶活性的影响[J].干旱区研究,2013(3):497-504.[34]王兴,于晶,杨阳,等.低温条件下不同抗寒性冬小麦内源激素的变化[J].麦类作物学报,2009,29(5):827-831.[35]罗正荣.植物激素与抗寒力的关系[J].植物生理学通讯,1989(3):1-5.[36]刘学庆,孙纪霞,丁朋松,等.低温胁迫对蝴蝶兰内源激素的影响[J].江西农业大学学报,2012,34(3):464-469.[37]WANG S W.Roles of cytokinin on stress-resistance and delaying senescence in plants[J].Chinese Bulletin of Botany,2000,17(2):121-126.[38]王丽丽,于锡宏.低地温对黄瓜幼苗内源GA3和IAA含量的影响[J].北方园艺,2004(3):44-45.[39]赵一航,孟令东,张晓萌,等.4个紫花苜蓿品种对低温胁迫的生理响应及抗寒性评价[J].草业科学,2021,38(4):683-692.

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Last Update: 2022-11-30