Phenylalanine ammonia-lyase 2 regulates secondary metabolism and confers manganese tolerance in Stylosanthes guianensis

被引:2
|
作者
Wang, Linjie [1 ,2 ]
Li, Jifu [1 ]
Liu, Liting [1 ]
Dong, Rongshu [1 ]
Liu, Guodao [1 ]
Rao, Idupulapati M. [3 ]
Chen, Zhijian [1 ,2 ]
机构
[1] Chinese Acad Trop Agr Sci, Trop Crops Genet Resources Inst, Key Lab Crop Gene Resources & Germplasm Enhancemen, Minist Agr & Rual Affairs, Haikou 571101, Peoples R China
[2] Chinese Acad Trop Agr Sci, Natl Key Lab Trop Crop Breeding, Sanya 572024, Peoples R China
[3] Int Ctr Trop Agr, Cali 763537, Colombia
基金
中国国家自然科学基金;
关键词
PAL GENE FAMILY; MEMBRANACEUS VAR. MONGHOLICUS; DIFFERENTIAL EXPRESSION; ACCUMULATION; PLANTS; HOMEOSTASIS; RESISTANCE; TOXICITY; ENZYMES; PATHWAY;
D O I
10.1093/plphys/kiaf005
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Stylo (Stylosanthes guianensis) is a tropical legume that exhibits considerable tolerance to manganese (Mn) toxicity, which severely constrains plant growth in acidic soils. To elucidate the Mn detoxification mechanisms in stylo, this study investigated the excess Mn-regulated metabolic profile of stylo roots and examined the role of metabolic enzymes in Mn tolerance. Excess Mn triggered oxidative stress in the 2 stylo genotypes tested. However, Mn-stimulated activation of antioxidant defense systems was observed in the Mn-tolerant genotype RY5 but not in the Mn-sensitive genotype TF0317. Metabolomic analysis of the Mn-tolerant RY5 roots revealed numerous excess Mn-responsive metabolites, mainly related to flavonoids and phenolic acids. Furthermore, a set of genes involved in the phenylpropanoid/flavonoid pathway were upregulated by excess Mn in stylo roots, especially in RY5. We characterized the excess Mn-inducible gene SgPAL2, encoding phenylalanine ammonia-lyase. SgPAL2 localized to the endoplasmic reticulum. Compared with control plants, SgPAL2 overexpression led to increases in shoot and root dry weights under Mn-excess conditions, whereas SgPAL2 suppression had the opposite effect. Moreover, SgPAL2 overexpression dramatically altered secondary metabolism, particularly flavonoid metabolism. In a bioassay, the inhibition of root elongation caused by excess Mn was alleviated by treatment with exogenous calycosin, an SgPAL2-regulated isoflavonoid, suggesting calycosin can detoxify Mn. Taken together, these findings indicate that SgPAL2 plays a critical role in enhancing Mn tolerance in stylo through metabolic regulation. The excess manganese-inducible gene SgPAL2 encodes phenylalanine ammonia-lyase, which enhances manganese tolerance in Stylosanthes guianensis by altering flavonoid metabolism.
引用
收藏
页数:18
相关论文
共 50 条
  • [1] PHENYLALANINE AMMONIA-LYASE AND PHENYLPROPANOID METABOLISM
    SERGEICHIK, AA
    FIZIOLOGIYA I BIOKHIMIYA KULTURNYKH RASTENII, 1987, 19 (03): : 211 - 220
  • [2] Structural basis for the entrance into the phenylpropanoid metabolism catalyzed by phenylalanine ammonia-lyase
    Ritter, H
    Schulz, GE
    PLANT CELL, 2004, 16 (12): : 3426 - 3436
  • [3] Phenylalanine ammonia-lyase and phenolic compounds in chamomile tolerance to cadmium and copper excess
    Kovacik, Jozef
    Backor, Martin
    WATER AIR AND SOIL POLLUTION, 2007, 185 (1-4): : 185 - 193
  • [4] Phenylalanine Ammonia-Lyase and Phenolic Compounds in Chamomile Tolerance to Cadmium and Copper Excess
    Jozef Kováčik
    Martin Bačkor
    Water, Air, and Soil Pollution, 2007, 185 : 185 - 193
  • [5] Malate Synthesis and Secretion Mediated by a Manganese-Enhanced Malate Dehydrogenase Confers Superior Manganese Tolerance in Stylosanthes guianensis
    Chen, Zhijian
    Sun, Lili
    Liu, Pandao
    Liu, Guodao
    Tian, Jiang
    Liao, Hong
    PLANT PHYSIOLOGY, 2015, 167 (01) : 176 - +
  • [6] METABOLISM OF AROMATIC AMINO ACID IN MICROORGANISMS .2. PROPERTIES OF PHENYLALANINE AMMONIA-LYASE OF RHODOTORULA
    OGATA, K
    UCHIYAMA, K
    YAMADA, H
    TOCHIKURA, T
    AGRICULTURAL AND BIOLOGICAL CHEMISTRY, 1967, 31 (05): : 600 - +
  • [7] Manganese (Mn2+)-dependent storage stabilization of Rhodotorula glutinis phenylalanine ammonia-lyase activity
    Wall, Mark J.
    Quinn, Andrew J.
    D'Cunha, Godwin B.
    JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2008, 56 (03) : 894 - 902
  • [8] CLONING AND SEQUENCE OF A CDNA-ENCODING PHENYLALANINE AMMONIA-LYASE FROM THE TROPICAL FORAGE LEGUME STYLOSANTHES HUMILIS
    MANNERS, JM
    MCINTYRE, CL
    NOURSE, JP
    PLANT PHYSIOLOGY, 1995, 108 (03) : 1301 - 1302
  • [9] The behavior of substrate analogues and secondary deuterium isotope effects in the phenylalanine ammonia-lyase reaction
    Gloge, A
    Langer, B
    Poppe, L
    Retey, J
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1998, 359 (01) : 1 - 7
  • [10] Role of phenylalanine ammonia-lyase in heat pretreatment-induced chilling tolerance in banana fruit
    Chen, Jian-ye
    He, Li-hong
    Jiang, Yue-ming
    Wang, Yong
    Joyce, Daryl C.
    Ji, Zuo-liang
    Lu, Wang-jin
    PHYSIOLOGIA PLANTARUM, 2008, 132 (03) : 318 - 328