Exploitation of tolerance to drought stress in carrot (Daucus carota L.): an overview

Muhammad Daniyal Junaid, Zahide Neslihan Öztürk, Ali Fuat Gökçe

Stress Biology ›› 2023, Vol. 3 ›› Issue (1) : 55. DOI: 10.1007/s44154-023-00130-0
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Exploitation of tolerance to drought stress in carrot (Daucus carota L.): an overview

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Abstract

Drought stress is a significant environmental factor that adversely affects the growth and development of carrot (Daucus carota L.), resulting in reduced crop yields and quality. Drought stress induces a range of physiological and biochemical changes in carrots, including reduced germination, hindered cell elongation, wilting, and disrupted photosynthetic efficiency, ultimately leading to stunted growth and decreased root development. Recent research has focused on understanding the molecular mechanisms underlying carrot's response to drought stress, identifying key genes and transcription factors involved in drought tolerance. Transcriptomic and proteomic analyses have provided insights into the regulatory networks and signaling pathways involved in drought stress adaptation. Among biochemical processes, water scarcity alters carrot antioxidant levels, osmolytes, and hormones. This review provides an overview of the effects of drought stress on carrots and highlights recent advances in drought stress-related studies on this crop. Some recent advances in understanding the effects of drought stress on carrots and developing strategies for drought stress mitigation are crucial for ensuring sustainable carrot production in the face of changing climate conditions. However, understanding the mechanisms underlying the plant's response to drought stress is essential for developing strategies to improve its tolerance to water scarcity and ensure food security in regions affected by drought.

Keywords

Carrots / Drought / Hormonal regulation / miRNAs / Metabolites / Quality

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Muhammad Daniyal Junaid, Zahide Neslihan Öztürk, Ali Fuat Gökçe. Exploitation of tolerance to drought stress in carrot (Daucus carota L.): an overview. Stress Biology, 2023, 3(1): 55 https://doi.org/10.1007/s44154-023-00130-0

References

[1]
AamirA, NaimaHN, AdeelIS, RameezH, MuhammadJ, AneelaN, SabaM, SamiaF, NasimAY, SimonPW. Phylogenetic relationship and screening of diverse germplasm of carrot (Daucus carota) for drought resistance. Fresenius Environ Bull, 2019, 28: 8474-8479
[2]
Ahmad T, Cawood M, Iqbal Q, Ariño A, Batool A, Tariq RMS, Azam M, Akhtar S (2019) Phytochemicals in Daucus carota and their health benefits. Foods 8:424. https://doi.org/10.3390/foods8090424
[3]
AndreCM, SchafleitnerR, GuignardC, OufirM, AliagaCAA, NombertoG, HoffmannL, HausmanJF, EversD, LarondelleY. Modification of the health-promoting value of potato tubers field grown under drought stress: emphasis on dietary antioxidant and glycoalkaloid contents in five native andean cultivars (Solanum tuberosum L). J Agr Food Chem, 2009, 57: 599-609
CrossRef Google scholar
[4]
AnjumNA, SofoA, ScopaA, RoychoudhuryA, GillSS, IqbalM, LukatkinAS, PereiraE, DuarteAC, AhmadI. Lipids and proteins—major targets of oxidative modifications in abiotic stressed plants. Environ Sci Poll Res, 2015, 22: 4099-4121
CrossRef Google scholar
[5]
AnnonA, RathoreK, CrosbyK. Overexpression of a tobacco osmotin gene in carrot (Daucus carota L) enhances drought tolerance. In Vitro Cell Dev Biol Plant, 2014, 50: 299-306
CrossRef Google scholar
[6]
AshrafMFMR, FooladMR. Roles of glycine betaine and proline in improving plant abiotic stress resistance. Environ Exp Bot, 2007, 59: 206-216
CrossRef Google scholar
[7]
BarozaiMYK, Saeed-ur-RehmanK, SarangzaiAM. Profiling the carrot (Daucus carota L) microRNAs and their targets. Pak J Bot, 2013, 45: 353-358
[8]
BashirR, RiazHN, AnwarS, ParveenN, KhalilzadehR, HussainI, MahmoodS. Morpho-physiological changes in carrots by foliar γ-aminobutyric acid under drought stress. Rev Bras Bot, 2021, 44: 57-68
CrossRef Google scholar
[9]
BlandoF, MarchelloS, MaioranoG, DuranteM, SignoreA, LausMN, SoccioM, MitaG. Bioactive compounds and antioxidant capacity in anthocyanin-rich carrots: a comparison between the black carrot and the Apulian landrace “Polignano” carrot. Plants, 2021, 10: 564
CrossRef Google scholar
[10]
BlumA. Osmotic adjustment is a prime drought stress adaptive engine in support of plant production. Plant Cell Environ, 2017, 40: 4-10
CrossRef Google scholar
[11]
BonasiaA, ConversaG, LazzizeraC, GambacortaG, EliaA. Morpho-biometrical nutritional and phytochemical characterization of carrot landraces from Puglia region (Southern Italy). Sustainability, 2021, 13: 3940
CrossRef Google scholar
[12]
BuchDU, SharmaOA, PableAA, BarvkarVT. Characterization of microRNA genes from Pigeonpea (Cajanus cajan L) and understanding their involvement in drought stress. J Biotech, 2020, 321: 23-34
CrossRef Google scholar
[13]
ChenX, DingY, YangY, SongC, WangB, YangS, GuoY, GongZ. Protein kinases in plant responses to drought, salt, and cold stress. J Int Plant Biol, 2021, 63: 53-78
CrossRef Google scholar
[14]
ČimoJ, AydınE, ŠinkaK, TárníkA, KiššV, HalajP, TokováL, KotušT. Change in the length of the vegetation period of tomato (Solanum lycopersicum L) white cabbage (Brassica oleracea L var capitata) and carrot (Daucus carota L) Due to climate change in Slovakia. Agronomy, 2020, 10: 1110
CrossRef Google scholar
[15]
CushmanJC, BohnertHJ. Genomic approaches to plant stress tolerance. Curr Opin Plant Biol, 2000, 3: 117-124
CrossRef Google scholar
[16]
DawoodMF, AzoozMM. Concentration-dependent effects of tungstate on germination growth lignification-related enzymes antioxidants and reactive oxygen species in broccoli (Brassica oleracea var italica L). Environ Sci Poll Res, 2019, 26: 36441-36457
CrossRef Google scholar
[17]
DuboisM, Van den BroeckL, InzéD. The pivotal role of ethylene in plant growth. Trend Plant Sci, 2018, 23: 311-323
CrossRef Google scholar
[18]
Elavarthi S, Martin B (2010) Spectrophotometric assays for antioxidant enzymes in plants. Methods Mol Biol. 639:273–281. https://doi.org/10.1007/978-1-60761-702-0_16.
[19]
FangY, XiongL. General mechanisms of drought response and their application in drought resistance improvement in plants. Cell Mol Life Sci, 2015, 72: 673-689
CrossRef Google scholar
[20]
FAO (2021) www.fao.org/statistics/. Accessed 28 Sept 2021.
[21]
Fasani E, DalCorso G, Zorzi G, Vitulo N, Furini A (2021) Comparative analysis identifies micro-RNA associated with nutrient homeostasis development and stress response in Arabidopsis thaliana upon high Zn and metal hyperaccumulator Arabidopsis helleri. Physiol Plant 173:920–934. https://doi.org/10.1111/ppl.13488
[22]
FraserCM, ChappleC. The phenylpropanoid pathway in Arabidopsis. The Arabidopsis book/American Society of Plant Biologists, 2011, 9: 152
[23]
GallHL, PhilippeF, DomonJM, GilletF, PellouxJ, RayonC. Cell wall metabolism in response to abiotic stress. Plants, 2015, 4: 112-166
CrossRef Google scholar
[24]
GillSS, AnjumNA, GillR, YadavS, HasanuzzamanM, FujitaM, MishraP, SabatSC, TutejaN. Superoxide dismutase—mentor of abiotic stress tolerance in crop plants. Environ Sci Pollut, 2015, 22: 10375-10394
CrossRef Google scholar
[25]
GorospeM, TominagaK, WuX, FählingM, IvanM. Post-transcriptional control of the hypoxic response by RNA-binding proteins and microRNAs. Front Mol Neurosci, 2011, 4: 7
CrossRef Google scholar
[26]
GrandaE, CamareroJJ. Drought reduces growth and stimulates sugar accumulation: new evidence of environmentally driven non-structural carbohydrate use. Tree Physiol, 2017, 37: 997-1000
CrossRef Google scholar
[27]
GrovesSJ, BaileyRJ. The effect of irrigation upon the root yield and incidence of common scab of carrots. Asp Appl Biol, 1994, 38: 217-221
[28]
GruneT, LietzG, PalouA, RossAC, StahlW, TangG, ThurnhamD, YinSA, BiesalskiHK. β-Carotene is an important vitamin A source for humans. J Nutr, 2010, 140: 2268S-2285S
CrossRef Google scholar
[29]
GuptaAJ, VermaTS, SethiS, SinghG. Evaluation of European carrot genotypes including F1 hybrids for their root quality yield and nutritive characters. Indian J Hortic, 2006, 63: 48-52
[30]
HaS, VankovaR, Yamaguchi-ShinozakiK, ShinozakiK, TranLSP. Cytokinins: metabolism and function in plant adaptation to environmental stresses. Trends Plant Sci, 2012, 17: 172-179
CrossRef Google scholar
[31]
HaberstrohS, KreuzwieserJ, Lobo-do-ValeR, CaldeiraMC, DubbertM, WernerC. Terpenoid emissions of two Mediterranean woody species in response to drought stress. Front Plant Sci, 2018, 9: 1071
CrossRef Google scholar
[32]
Hameed A, Akram NA, Saleem MH, Ashraf M, Ahmed S, Ali S, Abdullah Alsahli A, Alyemeni MN (2021) Seed treatment with α-tocopherol regulates growth and key physio-biochemical attributes in carrot (Daucus carota L.) plants under water limited regimes. Agronomy 11:469. https://doi.org/10.3390/agronomy11030469
[33]
HayatS, HayatQ, AlyemeniMN, WaniAS, PichtelJ, AhmadA. Role of proline under changing environments: a review. Plant Signal Behav, 2012, 7: 1456-1466
CrossRef Google scholar
[34]
HerppichWB, MempelH, GeyerM. Drought-and low temperature-acclimation in carrot (Daucus carota L.) roots. J Appl Bot, 2001, 75: 138-143
[35]
HoqueTS, HossainMA, MostofaMG, BurrittDJ, FujitaM, TranLSP. Methylglyoxal: an emerging signaling molecule in plant abiotic stress responses and tolerance. Front Plant Sci, 2016, 7: 1341
CrossRef Google scholar
[36]
HuangY, LiMY, WangF, XuZS, HuangW, WangGL, MaJ, XiongAS. Heat shock factors in carrot: genome-wide identification classification and expression profiles response to abiotic stress. Mol Biol Rep, 2015, 42: 893-905
CrossRef Google scholar
[37]
IqbalS, WangX, MubeenI, KamranM, KanwalI, DíazGA, AbbasA, ParveenA, AtiqMN, AlshayaH, Zin El-AbedinTK. Phytohormones trigger drought tolerance in crop plants: outlook and future perspectives. Front Plant Sci, 2022, 12: 3378
CrossRef Google scholar
[38]
JunaidMD, Öztürk GökçeZN, GökçeAF. Investigation of drought induced biochemical and gene expression changes in carrot cultivars. Mol Biol Rep, 2023, 50: 349-359
CrossRef Google scholar
[39]
JunaidMD, ÖztürkZN, GökçeAF. Drought stress effects on morphophysiological and quality characteristics of commercial carrot cultivars. Turk J Bot, 2023, 47: 111-126
CrossRef Google scholar
[40]
JunaidMD, ChaudhryUK, GökçeAF. Climate change and plant growth–South Asian perspective. Climate change plants, 2021 Boca Raton CRC Press 37-53
CrossRef Google scholar
[41]
JungYC, LeeHJ, YumSS, SohWY, ChoDY, AuhCK, LeeTK, SohHC, KimYS, LeeSC. Drought-inducible—but ABA-independent—thaumatin-like protein from carrot (Daucus carota L). Plant Cell Rep, 2005, 24: 366-373
CrossRef Google scholar
[42]
KamińskaI, LukasiewiczA, Klimek-ChodackaM, Długosz-GrochowskaO, RutkowskaJ, SzymonikK, BaranskiR. Antioxidative and osmoprotecting mechanisms in carrot plants tolerant to soil salinity. Sci Rep, 2022, 12: 1-15
CrossRef Google scholar
[43]
KanwarMK, YuJ, ZhouJ. Phytomelatonin: recent advances and future prospects. J Pineal Res, 2018, 65: 12526
CrossRef Google scholar
[44]
KeilwagenJ, LehnertH, BernerT, BudahnH, NothnagelT, UlrichD, DunemannF. The terpene synthase gene family of carrot (Daucus carota L): identification of QTLs and candidate genes associated with terpenoid volatile compounds. Front Plant Sci, 2017, 8: 1930
CrossRef Google scholar
[45]
KeutgenAJ, Tomaszewska-SowaM, BomberskiA, KeutgenN. The Influence of Phytohormones on the Efficiency of Callus Formation Its Morphologically Properties and Content of Bioactive Compounds in In Vitro Cultures of Daucus carota L. Hortic, 2022, 8: 100
CrossRef Google scholar
[46]
KhadrA, WangGL, WangYH, ZhangRR, WangXR, XuZS, TianYS, XiongAS. Effects of auxin (indole-3-butyric acid) on growth characteristics lignification and expression profiles of genes involved in lignin biosynthesis in carrot taproot. PeerJ, 2020, 8: 10492
CrossRef Google scholar
[47]
KhanMIR, FatmaM, PerTS, AnjumNA, KhanNA. Salicylic acid-induced abiotic stress tolerance and underlying mechanisms in plants. Front Plant Sci, 2015, 6: 462
CrossRef Google scholar
[48]
KodamaM, Brinch-PedersenH, SharmaS, HolmeIB, JoernsgaardB, DzhanfezovaT, AmbyDB, VieiraFG, LiuS, GilbertMTP. Identification of transcription factor genes involved in anthocyanin biosynthesis in carrot (Daucus carota L) using RNA-Seq. BMC Genom, 2018, 19: 1-13
CrossRef Google scholar
[49]
KowalczykZ, KubońM. Assessing the impact of water use in conventional and organic carrot production in Poland. Sci Rep, 2022, 12: 1-11
CrossRef Google scholar
[50]
KowalskaH, CzajkowskaK, CichowskaJ, LenartA. What's new in biopotential of fruit and vegetable by-products applied in the food processing industry. Trends Food Sci, 2017, 67: 150-159
CrossRef Google scholar
[51]
KumarM, Kumar PatelM, KumarN, BajpaiAB, SiddiqueKH. Metabolomics and molecular approaches reveal drought stress tolerance in plants. Int J Mol Sci, 2021, 22: 9108
CrossRef Google scholar
[52]
LandiM, TattiniM, GouldKS. Multiple functional roles of anthocyanins in plant-environment interactions. Environ Exp Bot, 2015, 119: 4-17
CrossRef Google scholar
[53]
LiW, WangY, ZhangY, WangR, GuoZ, et al.. Impacts of drought stress on the morphology, physiology, and sugar content of Lanzhou lily (Lilium davidii var. unicolor). Act Physiol Plant, 2020, 42: 1-11
CrossRef Google scholar
[54]
LiT, LiuJX, DengYJ, XuZS, XiongAS. Overexpression of a carrot BCH gene DcBCH1 improves tolerance to drought in Arabidopsis thaliana. BMC Plant Biol, 2021, 21: 1-13
CrossRef Google scholar
[55]
LiangC, WangW, MaJ, WangJ, ZhouF, LiW, YuY, ZhangL, HuangW, HuangX. Identification of differentially expressed microRNAs of sunflower seedlings under drought stress. Agron J, 2020, 112: 2472-2484
CrossRef Google scholar
[56]
LiaoH, WangQ, ZhangN, FuY, WuG, RenX, XueB, LiuX, XuZ, YanC. High-throughput microRNA and mRNA sequencing reveals that microRNAs may be involved in peroxidase-mediated cold tolerance in potato. Plant Mol Biol Rep, 2021, 39: 577-594
CrossRef Google scholar
[57]
MaJ, LiJ, XuZ, WangF, XiongA. Transcriptome profiling of genes involving in carotenoid biosynthesis and accumulation between leaf and root of carrot (Daucus carota L). Acta Biochim Biophys Sin, 2018, 50: 481-490
CrossRef Google scholar
[58]
Macko-PodgórniA, StelmachK, KwolekK, MachajG, EllisonS, SenalikDA, SimonPW, GrzebelusD. Mining for candidate genes controlling secondary growth of the carrot storage root. Int J Mol Sci, 2020, 21: 4263
CrossRef Google scholar
[59]
MahmoodT, KhalidS, AbdullahM, AhmedZ, ShahMKN, GhafoorA, DuX. Insights into drought stress signaling in plants and the molecular genetic basis of cotton drought tolerance. Cells, 2019, 9: 105
CrossRef Google scholar
[60]
Majidi MM, Rashidi F, Sharafi Y (2015) Physiological traits related to drought tolerance in Brassica. Int J Plant Prod 9:541–559. https://doi.org/10.22069/IJPP.2015.2462
[61]
GocanTM, MăniuţiuDN, BalcăuAI, S, Lazăr V, Bogdan I,. Sugar content of carrot roots influenced by the sowing period. J Hortic Forest Biotechnol, 2013, 17: 66-69
[62]
MurtiGSR, UpretiKK. Plant Growth Regulators in Water Stress Tolerance. J Hortic Sci, 2007, 2: 73-93
CrossRef Google scholar
[63]
NaingAH, KimCK. Abiotic stress-induced anthocyanins in plants: their role in tolerance to abiotic stresses. Physiol Plant, 2021, 172: 1711-1723
CrossRef Google scholar
[64]
NanH, GaoLZ. Genome-wide analysis of WRKY genes and their response to hormone and mechanic stresses in carrot. Front Gen, 2019, 10: 363
CrossRef Google scholar
[65]
ObidiegwuJE, BryanGJ, JonesHG, PrasharA. Coping with drought: stress and adaptive responses in potato and perspectives for improvement. Front Plant Sci, 2015, 6: 542
CrossRef Google scholar
[66]
OzturkM, Turkyilmaz UnalB, García-CaparrósP, KhursheedA, GulA, HasanuzzamanM. Osmoregulation and its actions during the drought stress in plants. Physiol Plant, 2021, 172: 1321-1335
CrossRef Google scholar
[67]
Öztürk GökçeZN, GökçeAF, JunaidMD, ChaudhryUK. Comparative transcriptomics of drought stress response of taproot meristem region of contrasting purple carrot breeding lines supported by physio-biochemical parameters. Funct Integr Genomics., 2022, 22: 697-710
CrossRef Google scholar
[68]
PaganoL, RossiR, PaesanoL, MarmiroliN, MarmiroliM. miRNA regulation and stress adaptation in plants. Environ Exp Bot, 2021, 184: 104369
CrossRef Google scholar
[69]
ParidaAK, DagaonkarVS, PhalakMS, UmalkarGV, AurangabadkarLP. Alterations in photosynthetic pigments protein and osmotic components in cotton genotypes subjected to short-term drought stress followed by recovery. Plant Biotech Rep, 2007, 1: 37-48
CrossRef Google scholar
[70]
ParkhiV, KumarV, SunilkumarG, CampbellLM, SinghNK, RathoreKS. Expression of apoplastically secreted tobacco osmotin in cotton confers drought tolerance. Mol Breed, 2009, 23: 625-639
CrossRef Google scholar
[71]
PolaniaJA, PoschenriederC, BeebeS, RaoIM. Effective use of water and increased dry matter partitioned to grain contribute to yield of common bean improved for drought resistance. Front Plant Sci, 2016, 7: 660
CrossRef Google scholar
[72]
PraxedesSC, DaMattaFM, LoureiroME, FerraoMA, CordeiroAT. Effects of long-term soil drought on photosynthesis and carbohydrate metabolism in mature robusta coffee (Coffea canephora Pierre var kouillou) leaves. Environ Exp Bot, 2006, 56: 263-273
CrossRef Google scholar
[73]
PriyaM, SharmaL, KaurR, BindumadhavaH, NairRM, SiddiqueKHM, NayyarH. GABA (γ-aminobutyric acid) as a thermo-protectant to improve the reproductive function of heat-stressed mungbean plants. Sci Rep, 2019, 9: 7788
CrossRef Google scholar
[74]
QaderiMM, MartelAB, DixonSL. Environmental factors influence plant vascular system and water regulation. Plants, 2019, 8: 65
CrossRef Google scholar
[75]
QueF, HouXL, WangGL, XuZS, TanGF, LiT, WangYH, KhadrA, XiongAS. Advances in research on the carrot an important root vegetable in the Apiaceae family. Hortic Res, 2019, 6: 69
CrossRef Google scholar
[76]
Quiroz-IturraLF, SimpsonK, AriasD, SilvaC, González-CalquinC, AmazaL, HandfordM, StangeC. Carrot DcALFIN4 and DcALFIN7 Transcription Factors Boost Carotenoid Levels and Participate Differentially in Salt Stress Tolerance When Expressed in Arabidopsis thaliana and Actinidia deliciosa. Int J Mol Sci, 2022, 23: 12157
CrossRef Google scholar
[77]
RaoAV, RaoLG. Carotenoids and Human Health. Pharma Res, 2007, 55: 207-216
CrossRef Google scholar
[78]
RazzaqM, AkramNA, AshrafM, NazH, Al-QurainyF. Interactive effect of drought and nitrogen on growth some key physiological attributes and oxidative defense system in carrot (Daucus carota L) plants. Sci Hortic, 2017, 225: 373-379
CrossRef Google scholar
[79]
ReidJB, GillespieRN. Yield and quality responses of carrots (Daucus carota L) to water deficits. N Z J Crop Hortic Sci, 2017, 45: 299-312
CrossRef Google scholar
[80]
RejebKB, AbdellyC, SavouréA. How reactive oxygen species and proline face stress together. Plant Physiol Biochem, 2014, 80: 278-284
CrossRef Google scholar
[81]
RenJ, ZhangH, ShiX, AiX, DongJ, ZhaoX, ZhongC, JiangC, WangJ, YuH. Genome-wide identification of key candidate microRNAs and target genes associated with peanut drought tolerance. DNA Cell Biol, 2021, 40: 373-383
CrossRef Google scholar
[82]
Salter PJ, Goode JE (1967) Crop responses to water at different stages of growth Crop responses to water at different stages of growth. https://doi.org/10.2136/sssaj1969.03615995003300010002x
[83]
SamuolienėG, DuchovskisP, UrbonavičiūtėA. Phytohormones dynamics during flowering initiation in carrots. Act Biol Szegediensis, 2005, 49: 33-37
[84]
SankarB, JaleelCA, ManivannanP, KishorekumarA, SomasundaramR, PanneerselvamR. Drought-induced biochemical modifications and proline metabolism in Abelmoschus esculentus (L) Moench. Act Bot Croatica, 2007, 66: 43-56
CrossRef Google scholar
[85]
SlabbertMM, KrügerGHJ. Antioxidant enzyme activity proline accumulation leaf area and cell membrane stability in water stressed Amaranthus leaves. S Afr J Bot, 2014, 95: 123-128
CrossRef Google scholar
[86]
SørensenJN, JørgensenU, KühnBF. Drought effects on the marketable and nutritional quality of carrots. J Sci Food Agric, 1997, 74: 379-391
CrossRef Google scholar
[87]
Taiz L, Zeiger E (2010) Plant physiology 5th Ed. Sunderland, MA Sinauer Associates, 464
[88]
TreutterD. Significance of flavonoids in plant resistance: a review. Environ Chem Lett, 2006, 4: 147-157
CrossRef Google scholar
[89]
WangGL, QueF, XuZS, WangF, XiongAS. Exogenous gibberellin altered morphology, anatomic and transcriptional regulatory networks of hormones in carrot root and shoot. BMC Plant Biol, 2015, 15: 1-12
CrossRef Google scholar
[90]
WangH, ZouS, LiY, LinF, TangD. An ankyrin-repeat and WRKY-domaincontaining immune receptor confers stripe rust resistance in wheat. Nat Commun, 2020, 11: 1-11
CrossRef Google scholar
[91]
WangM, TongS, MaT, XiZ, LiuJ. Chromosome-level genome assembly of Sichuan pepper provides insights into apomixis drought tolerance and alkaloid biosynthesis. Mol Ecol Res, 2021, 21: 2533-2545
CrossRef Google scholar
[92]
WeidnerS, KarolakM, KaramacM, KosinskaA, AmarowiczR. Phenolic compounds and properties of antioxidants in grapevine roots [Vitis vinifera L] under drought stress followed by recovery. Act Soc Botanic Pol, 2009, 78: 97-103
CrossRef Google scholar
[93]
WróbelM, KaramaM, AmarowiczR, Fr czek E, Weidner S,. Metabolism of phenolic compounds in Vitis riparia seeds during stratification and during germination under optimal and low temperature stress conditions. Act Physiol Plant, 2005, 27: 313-320
CrossRef Google scholar
[94]
XuZS, TanHW, WangF, HouXL, XiongAS. CarrotDB: a genomic and transcriptomic database for carrot. Database., 2014, 2014: 1-8
CrossRef Google scholar
[95]
YangX, LuM, WangY, WangY, LiuZ, ChenS. Response mechanism of plants to drought stress. Hortic, 2021, 7: 50
CrossRef Google scholar
[96]
YaoT, ZhangJ, XieM, YuanG, TschaplinskiTJ, MucheroW, ChenJG. Transcriptional regulation of drought response in Arabidopsis and woody plants Front. Plant Sci, 2021, 11: 572137
CrossRef Google scholar
[97]
YuSM. Cellular and genetic responses of plants to sugar starvation. Plant Physiol, 1999, 121: 687-693
CrossRef Google scholar
[98]
ZhangRR, WangYH, LiT, TanGF, TaoJP, SuXJ, XuZS, TianYS, XiongAS. Effects of simulated drought stress on carotenoid contents and expression of related genes in carrot taproots. Protoplasma, 2021, 258: 379-390
CrossRef Google scholar
[99]
ZhuC, ZhangS, ZhouC, XieS, ChenG, TianC, XuK, LinY, LaiZ, GuoY. Genome-wide investigation of N6-methyladenosine regulatory genes and their roles in tea (Camellia sinensis) leaves during withering process. Front Plant Sci, 2021, 12: 702303
CrossRef Google scholar

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