作物栽培与生理 |
|
|
|
|
外源5-氨基乙酰丙酸对油菜幼苗硫代葡萄糖苷生物合成的影响(英文) |
MAODZEKA Antony,卢凌志,赵鑫泽,徐颖,吴德志,蒋立希* |
浙江大学农业与生物技术学院,浙江省作物种质资源重点实验室,杭州 310058 |
|
Effect of exogenous 5-aminolevulinic acid on glucosinolate biosynthesis in rape (Brassica napus L.) seedlings |
Antony MAODZEKA(),Lingzhi LU,Xinze ZHAO,Ying XU,Dezhi WU,Lixi JIANG() |
Zhejiang Key Laboratory of Crop Gene Resources, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310058, China |
引用本文:
MAODZEKA Antony, 卢凌志, 赵鑫泽, 徐颖, 吴德志, 蒋立希. 外源5-氨基乙酰丙酸对油菜幼苗硫代葡萄糖苷生物合成的影响(英文)[J]. 浙江大学学报(农业与生命科学版), 2020, 46(3): 291-307.
Antony MAODZEKA, Lingzhi LU, Xinze ZHAO, Ying XU, Dezhi WU, Lixi JIANG. Effect of exogenous 5-aminolevulinic acid on glucosinolate biosynthesis in rape (Brassica napus L.) seedlings. Journal of Zhejiang University (Agriculture and Life Sciences), 2020, 46(3): 291-307.
链接本文:
http://www.zjujournals.com/agr/CN/10.3785/j.issn.1008-9209.2019.08.262
或
http://www.zjujournals.com/agr/CN/Y2020/V46/I3/291
|
1 |
HOTTA Y, TANAKA T, TAKAOKA H, et al. New physiological effects of 5-aminolevulinic acid in plants: the increase of photosynthesis, chlorophyll content, and plant growth. Bioscience, Biotechnology, and Biochemistry, 1997,61(12):2025-2028. DOI:10.1271/bbb.61.2025
doi: 10.1271/bbb.61.2025
|
2 |
CHEN G, FAN P S, FENG W M, et al. Effects of 5-aminolevulinic acid on nitrogen metabolism and ion distribution of watermelon seedlings under salt stress. Russian Journal of Plant Physiology, 2017,64(1):116-123. DOI:10.1134/S1021443717010046
doi: 10.1134/S1021443717010046
|
3 |
ZHANG W F, ZHANG F, RAZIUDDIN R, et al. Effects of 5-aminolevulinic acid on oilseed rape seedling growth under herbicide toxicity stress. Journal of Plant Growth Regulation, 2008,27:159-169. DOI:10.1007/s00344-008-9042-y
doi: 10.1007/s00344-008-9042-y
|
4 |
TIAN T, ALI B, QIN Y B, et al. Alleviation of lead toxicity by 5-aminolevulinic acid is related to elevated growth, photosynthesis, and suppressed ultrastructural damages in oilseed rape. BioMed Research International, 2014,2014:530642. DOI:10.1155/2014/530642
doi: 10.1155/2014/530642
|
5 |
FU J J, CHU X T, SUN Y F, et al. Involvement of nitric oxide in 5-aminolevulinic acid-induced antioxidant defense in roots of Elymus nutans exposed to cold stress. Biologia Plantarum, 2016,60(3):585-594. DOI:10.1007/s10535-016-0635-1
doi: 10.1007/s10535-016-0635-1
|
6 |
MARUYAMA-NAKASHITA A, HIRAI M Y, FUNADA S. Exogenous application of 5-aminolevulinic acid increases the transcript levels of sulfur transport and assimilatory genes, sulfate uptake, and cysteine and glutathione contents in Arabidopsis thaliana. Soil Science and Plant Nutrition, 2010,56(2):281-288. DOI:10.1111/j.1747-0765.2010.00458.x
doi: 10.1111/j.1747-0765.2010.00458.x
|
7 |
FOYER C H, THEODOULOU F L, DELROT S. The functions of inter- and intracellular-glutathione transport systems in plants. Trends in Plant Science, 2001,6(10):486-492. DOI:10.1016/s1360-1385(01)02086-6
doi: 10.1016/s1360-1385(01)02086-6
|
8 |
FALK K L, TOKUHISA J G, GERSHENZON J. The effect of sulfur nutrition on plant glucosinolate content: physiology and molecular mechanisms. Plant Biology, 2007,9:573-581. DOI:10.1055/s-2007-965431
doi: 10.1055/s-2007-965431
|
9 |
BORPATRAGOHAIN P, ROSE T J, KING G J. Fire and brimstone: molecular interactions between sulfur and glucosinolate biosynthesis in model and crop Brassicaceae. Frontiers in Plant Science, 2016,7:1735. DOI:10.3389/fpls.2016.01735
doi: 10.3389/fpls.2016
|
10 |
S?NDERBY I E, GEU-FLORES F, HALKIER B A. Biosynthesis of glucosinolates-gene discovery and beyond. Trends in Plant Science, 2010,15(5):283-290. DOI:10.1016/j.tplants.2010.02.005
doi: 10.1016/j.tplants.2010.02.005
|
11 |
HALKIER B A, GERSHENZON J. Biology and biochemistry of glucosinolates. Annual Review of Plant Biology, 2006,57:303-333. DOI:10.1146/annurev.arplant.57.032905.105228
doi: 10.1146/annurev.arplant.57.032905.105228
|
12 |
PI?LEWSKA-BEDNAREK M, NAKANO R T, HIRUMA K, et al. Glutathione transferase U13 functions in pathogen-triggered glucosinolate metabolism. Plant Physiology, 2018,176:538-551. DOI:10.1104/pp.17.01455
doi: 10.1104/pp.17.01455
|
13 |
BANERJEE A, RAI A N, PENNA S, et al. Aliphatic glucosinolate synthesis and gene expression changes in gamma-irradiated cabbage. Food Chemistry, 2016,209:99-103. DOI:10.1016/j.foodchem.2016.04.022
doi: 10.1016/j.foodchem.2016.04.022
|
14 |
GUO R F, SHEN W S, QIAN H M, et al. Jasmonic acid and glucose synergistically modulate the accumulation of glucosinolates in Arabidopsis thaliana. Journal of Experimental Botany, 2013,64(18):5707-5719. DOI:10.1093/jxb/ert348
doi: 10.1093/jxb/ert348
|
15 |
MIAO H Y, WEI J, ZHAO Y T, et al. Glucose signalling positively regulates aliphatic glucosinolate biosynthesis. Journal of Experimental Botany, 2013,64(4):1097-1109. DOI:10.1093/jxb/ers399
doi: 10.1093/jxb/ers399
|
16 |
OMIROU M D, PAPADOPOULOU K K, PAPASTYLIANOU I, et al. Impact of nitrogen and sulfur fertilization on the composition of glucosinolates in relation to sulfur assimilation in different plant organs of broccoli. Journal of Agricultural and Food Chemistry, 2009,57(20):9408-9417. DOI:10.1021/jf901440n
doi: 10.1021/jf901440n
|
17 |
JIANG Y F, LI J L, CALDWELL C D. Glucosinolate content of camelina genotypes as affected by applied nitrogen and sulphur. Crop Science, 2016,56(6):3250. DOI:10.2135/cropsci2016.01.0018
doi: 10.2135/cropsci2016.01.0018
|
18 |
MIKKELSEN M D, NAUR P, HALKIER B A. Arabidopsis mutants in the C-S lyase of glucosinolate biosynthesis establish a critical role for indole-3-acetaldoxime in auxin homeostasis. The Plant Journal, 2004,37(5):770-777. DOI:10.1111/j.1365-313X.2004.02002.x
doi: 10.1111/j.1365-313X.2004.02002.x
|
19 |
TAKAHASHI H, KOPRIVA S, GIORDANO M, et al. Sulfur assimilation in photosynthetic organisms: molecular functions and regulations of transporters and assimilatory enzymes. Annual Review of Plant Biology, 2011,62:157-184. DOI:10.1146/annurev-arplant-042110-103921
doi: 10.1146/annurev-arplant-042110-103921
|
20 |
BONES A M, VISVALINGAM S, THANGSTAD O P. Sulphate can induce differential expression of thioglucoside glucohydrolases (myrosinases). Planta, 1994,193(4):558-566.
|
21 |
WAWRZY?SKA A, SIRKO L, HAWKESFORD M J, et al. Biochemical analysis of transgenic tobacco lines producing bacterial serine acetyltransferase. Plant Science, 2002,162(4):589-597. DOI: 10.1016/s0168-9452(01)00598-2
doi: 10.1016/s0168-9452(01)00598-2
|
22 |
MINOCHA R, THANGAVEL P, DHANKHER O P, et al. Separation and quantification of monothiols and phytochelatins from a wide variety of cell cultures and tissues of trees and other plants using high performance liquid chromatography. Journal of Chromatography A, 2008,1207(1/2):72-83. DOI:10.1016/j.chroma.2008.08.023
doi: 10.1016/j.chroma.2008.08.023
|
23 |
BRADFORD M M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry, 1976,72:248-254.
|
24 |
SAITO K, KUROSAWA M, TATSUGUCHI K, et al. Modulation of cysteine biosynthesis in chloroplasts of transgenic tobacco overexpressing cysteine synthase [O-acetylserine (thiol)-iyase]. Plant Physiology, 1994,106(3):887-895.
|
25 |
GAITONDE M K. A spectrophotometric method for the direct determination of cysteine in the presence of other naturally occurring amino acids. Biochemical Journal, 1967,104(2):627-633.
|
26 |
BOOTH J, BOYLAND E, SIMS P. An enzyme from rat liver catalysing conjugations with glutathione. The Biochemical Journal, 1961,79(3):516-524.
|
27 |
ISLAM M R, CHOWDHURY A K, RAHMAN M M, et al. Comparative investigation of glutathione S-transferase (GST) in different crops and purification of high active GSTs from onion (Allium cepa L.). Journal of Plant Sciences, 2015,3(3):162-170. DOI:10.11648/j.jps.20150303.17
doi: 10.11648/j.jps.20150303.17
|
28 |
KLIEBENSTEIN D J, KROYMANN J, BROWN P D, et al. Genetic control of natural variation in Arabidopsis glucosinolate accumulation. Plant Physiology, 2001,126(2):811-825. DOI:10.1104/pp.126.2.811
doi: 10.1104/pp.126.2.811
|
29 |
BROWN P D, TOKUHISA J G, REICHELT M. Variation of glucosinolate accumulation among different organs and developmental stages of Arabidopsis thaliana. Phytochemistry, 2003,62(3):471-481. DOI:10.1016/S0031-9422(02)00549-6
doi: 10.1016/S0031-9422(02)00549-6
|
30 |
BUROW M, MüLLER R, GERSHENZON J, et al. Altered glucosinolate hydrolysis in genetically engineered Arabidopsis thaliana and its influence on the larval development of Spodoptera littoralis. Journal of Chemical Ecology, 2006,32(11):2333-2349. DOI:10.1007/s10886-006-9149-1
doi: 10.1007/s10886-006-9149-1
|
31 |
GUO L P, YANG R Q, WANG Z Y, et al. Glucoraphanin, sulforaphane and myrosinase activity in germinating broccoli sprouts as affected by growth temperature and plant organs. Journal of Functional Foods, 2014,9:70-77. DOI:10.1016/j.jff.2014.04.015
doi: 10.1016/j.jff.2014.04.015
|
32 |
BEAUDOINEAGAN L D, THORPE T A. Tyrosine and phenylalanine ammonia lyase activities during shoot initiation in tobacco callus cultures. Plant Physiology, 1985,78(3):438-441.
|
33 |
GANAPATHY G, KEERTHI D, NAIR R A, et al. Correlation of phenylalanine ammonia lyase (PAL) and tyrosine ammonia lyase (TAL) activities to phenolics and curcuminoid content in ginger and its wild congener, Zingiber zerumbet following Pythium myriotylum infection. European Journal of Plant Pathology, 2016,145(4):777-785. DOI:10.1007/s10658-016-0865-2
doi: 10.1007/s10658-016-0865-2
|
34 |
TRIPATHY B C, CHAKRABORTY N. 5-aminolevulinic acid induced photodynamic damage of the photosynthetic electron transport chain of cucumber (Cucumis sativus L.) cotyledons. Plant Physiology, 1991,96(3):761-767.
|
35 |
CHAKRABORTY N, TRIPATHY B C. Involvement of singlet oxygen in 5-aminolevulinic acid-induced photodynamic damage of cucumber (Cucumis sativus L.) chloroplasts. Plant Physiology, 1992,98(1):7-11.
|
36 |
CARTEA M E, FRANCISCO M, SOENGAS P, et al. Phenolic compounds in Brassica vegetables. Molecules, 2011,16(1):251-280. DOI:10.3390/molecules16010251
doi: 10.3390/molecules16010251
|
37 |
HIRAI M Y, KLEIN M, FUJIKAWA Y, et al. Elucidation of gene-to-gene and metabolite-to-gene networks in Arabidopsis by integration of metabolomics and transcriptomics. Journal of Biological Chemistry, 2005,280(27):25590-25595. DOI:10.1074/jbc.M502332200
doi: 10.1074/jbc.M502332200
|
38 |
CHEN X J, ZHU Z J, NI X L, et al. Effect of nitrogen and sulfur supply on glucosinolates in Brassica campestris ssp. chinensis. Agricultural Sciences in China, 2006,5(8):603-608. DOI:10.1016/s1671-2927(06)60099-0
doi: 10.1016/s1671-2927(06)60099-0
|
39 |
LJUNG K, HULL A K, CELENZA J L, et al. Sites and regulation of auxin biosynthesis in Arabidopsis roots. The Plant Cell, 2005,17(4):1090-1104. DOI:10.1105/tpc.104.029272
doi: 10.1105/tpc.104.029272
|
40 |
ZHAO Y D, HULL A K, GUPTA N R, et al. Trp-dependent auxin biosynthesis in Arabidopsis: involvement of cytochrome P450s CYP79B2 and CYP79B3. Genes and Development, 2002,16(23):3100-3112. DOI:10.1101/gad.1035402
doi: 10.1101/gad.1035402
|
41 |
NIU K J, MA H L. The positive effects of exogenous 5-aminolevulinic acid on the chlorophyll biosynthesis, photosystem and calvin cycle of Kentucky bluegrass seedlings in response to osmotic stress. Environmental and Experimental Botany, 2018,155:260-271. DOI:10.2753/REE1540-496X440306
doi: 10.2753/REE
|
|
Viewed |
|
|
|
Full text
|
|
|
|
|
Abstract
|
|
|
|
|
Cited |
|
|
|
|
|
Shared |
|
|
|
|
|
Discussed |
|
|
|
|