Identification and characterization of transition metal-binding proteins and metabolites in the phloem sap of Brassica napus

被引:0
|
作者
Kupper, Hendrik [1 ,2 ]
Gokul, Arun [3 ]
Alavez, Dario [4 ]
Dhungana, Singha R. [5 ]
Bokhari, Syed Nadeem Hussain [1 ]
Keyster, Marshall [6 ]
Mendoza-Cozatl, David G. [4 ,6 ]
机构
[1] Czech Acad Sci, Inst Plant Mol Biol, Biol Ctr, Lab Plant Biophys & Biochem, Ceske Budejovice, Czech Republic
[2] Univ South Bohemia, Dept Expt Plant Biol, Ceskeeske Budejovice, Czech Republic
[3] Univ Free State, Dept Plant Sci, Qwaqwa Campus, Phuthaditjhaba, South Africa
[4] Univ Missouri Columbia, Div Plant Sci, Columbia, MO 65211 USA
[5] Univ Missouri Columbia, Div Biol Sci, Columbia, MO USA
[6] Univ Western Cape, Dept Biotechnol, Environm Biotechnol Lab, Bellville, South Africa
基金
美国国家科学基金会;
关键词
LONG-DISTANCE TRANSPORT; IRON; CADMIUM; ACCUMULATION; METALLOTHIONEINS; PHYTOCHELATINS; TRAFFICKING; EXPRESSION; LEAVES;
D O I
10.1016/j.jbc.2024.107741
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transition metal (TM) distribution through the phloem is an essential part of plant metabolism and is required for systemic signaling and balancing source-to-sink relationships. Due to their reactivity, TMs are expected to occur in complexes within the phloem sap; however, metal speciation in the phloem sap remains largely unexplored. Here, we isolated phloem sap from Brassica napus and analyzed it via size exclusion chromatography coupled online to sector-field ICP-MS. Our data identified known TM-binding proteins and molecules including metallothioneins (MT), glutathione, and nicotianamine. While the main peak of all metals was low MW (similar to 1.5 kD), additional peaks similar to 10 to 15 kD containing Cu, Fe, S, and Zn were also found. Further physicochemical analyses of MTs with and without affinity tags corroborated that MTs can form complexes of diverse molecular weights. We also identifiedand characterized potential artifacts in the TM-biding ability of B. napus MTs between tagged and non-tagged MTs. That is, the native BnMT2 binds Zn, Cu, and Fe, while MT3a and MT3b only bind Cu and Zn. In contrast, his-tagged MTs bind less Cu and were found to bind Co and Mn and aggregated to oligomeric forms to a greater extent compared to the phloem sap. Our data indicates that TM chemistry in the phloem sap is more complex than previously anticipated and that more systematic analyses are needed to establish the precise speciation of TM and TM-ligand complexes within the phloem sap.
引用
收藏
页数:14
相关论文
共 50 条
  • [1] Towards the proteome of Brassica napus phloem sap
    Giavalisco, P
    Kapitza, K
    Kolasa, A
    Buhtz, A
    Kehr, J
    PROTEOMICS, 2006, 6 (03) : 896 - 909
  • [2] Identification and characterization of small RNAs from the phloem of Brassica napus
    Buhtz, Anja
    Springer, Franziska
    Chappell, Louise
    Baulcombe, David C.
    Kehr, Julia
    PLANT JOURNAL, 2008, 53 (05): : 739 - 749
  • [3] Effects of Fe deficiency on the protein profile of Brassica napus phloem sap
    Gutierrez-Carbonell, Elain
    Lattanzio, Giuseppe
    Albacete, Alfonso
    Rios, Juan Jose
    Kehr, Julia
    Abadia, Anunciacion
    Grusak, Michael A.
    Abadia, Javier
    Flor Lopez-Millan, Ana
    PROTEOMICS, 2015, 15 (22) : 3835 - 3853
  • [4] THE PREDICTION AND CHARACTERIZATION OF METAL-BINDING SITES IN PROTEINS
    GREGORY, DS
    MARTIN, ACR
    CHEETHAM, JC
    REES, AR
    PROTEIN ENGINEERING, 1993, 6 (01): : 29 - 35
  • [5] Analysis of xylem sap proteins from Brassica napus
    Julia Kehr
    Anja Buhtz
    Patrick Giavalisco
    BMC Plant Biology, 5
  • [6] Analysis of xylem sap proteins from Brassica napus
    Kehr, Julia
    Buhtz, Anja
    Giavalisco, Patrick
    BMC PLANT BIOLOGY, 2005, 5 (1)
  • [7] Identification, characterization and determination of metal-binding proteins by liquid chromatography.: A review
    Guntiñas, MBDC
    Bordin, G
    Rodriguez, AR
    ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2002, 374 (03) : 369 - 378
  • [8] Identification, characterization and determination of metal-binding proteins by liquid chromatography. A review
    M. de la Calle Guntiñas
    G. Bordin
    A. Rodriguez
    Analytical and Bioanalytical Chemistry, 2002, 374 : 369 - 378
  • [9] METAL-BINDING PROTEINS AND METAL TOXICITY
    不详
    MARINE POLLUTION BULLETIN, 1981, 12 (07) : 230 - 231
  • [10] METAL-BINDING SITES IN PROTEINS
    TAINER, JA
    ROBERTS, VA
    GETZOFF, ED
    CURRENT OPINION IN BIOTECHNOLOGY, 1991, 2 (04) : 582 - 591