Two carbon fluxes to reserve starch in potato (Solanum tuberosum L.) tuber cells are closely interconnected but differently modulated by temperature

被引:34
作者
Fettke, Joerg [1 ]
Leifels, Lydia [1 ]
Brust, Henrike [1 ]
Herbst, Karoline [1 ]
Steup, Martin [1 ]
机构
[1] Univ Potsdam, Inst Biochem & Biol, Dept Plant Physiol, D-14476 Potsdam, Germany
关键词
glucose; 1-phosphate; phosphorylase; potato tubers; starch; starch synthase; ALPHA-GLUCAN PHOSPHORYLASE; BIOSYNTHETIC-ENZYMES; ANTISENSE INHIBITION; GLUCOSE; 1-PHOSPHATE; METABOLISM; AMYLOPLASTS; PLANT; PHOSPHOGLUCOMUTASE; ARABIDOPSIS; EXPRESSION;
D O I
10.1093/jxb/ers014
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Parenchyma cells from tubers of Solanum tuberosum L. convert several externally supplied sugars to starch but the rates vary largely. Conversion of glucose 1-phosphate to starch is exceptionally efficient. In this communication, tuber slices were incubated with either of four solutions containing equimolar [U-C-14]glucose 1-phosphate, [U-C-14]sucrose, [U-C-14]glucose 1-phosphate plus unlabelled equimolar sucrose or [U-C-14]sucrose plus unlabelled equimolar glucose 1-phosphate. C-14-incorporation into starch was monitored. In slices from freshly harvested tubers each unlabelled compound strongly enhanced C-14 incorporation into starch indicating closely interacting paths of starch biosynthesis. However, enhancement disappeared when the tubers were stored. The two paths (and, consequently, the mutual enhancement effect) differ in temperature dependence. At lower temperatures, the glucose 1-phosphate-dependent path is functional, reaching maximal activity at approximately 20 degrees C but the flux of the sucrose-dependent route strongly increases above 20 degrees C. Results are confirmed by in vitro experiments using [U-C-14]glucose 1-phosphate or adenosine-[U-C-14]glucose and by quantitative zymograms of starch synthase or phosphorylase activity. In mutants almost completely lacking the plastidial phosphorylase isozyme(s), the glucose 1-phosphate-dependent path is largely impeded. Irrespective of the size of the granules, glucose 1-phosphate-dependent incorporation per granule surface area is essentially equal. Furthermore, within the granules no preference of distinct glucosyl acceptor sites was detectable. Thus, the path is integrated into the entire granule biosynthesis. In vitro C-14-incorporation into starch granules mediated by the recombinant plastidial phosphorylase isozyme clearly differed from the in situ results. Taken together, the data clearly demonstrate that two closely but flexibly interacting general paths of starch biosynthesis are functional in potato tuber cells.
引用
收藏
页码:3011 / 3029
页数:19
相关论文
共 46 条
  • [1] Homodimers and heterodimers of Pho1-type phosphorylase isoforms in Solanum tuberosum L. as revealed by sequence-specific antibodies
    Albrecht, T
    Greve, B
    Pusch, K
    Kossmann, J
    Buchner, P
    Wobus, U
    Steup, M
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1998, 251 (1-2): : 343 - 352
  • [2] From bacterial glycogen to starch: Understanding the biogenesis of the plant starch granule
    Ball, SG
    Morell, MK
    [J]. ANNUAL REVIEW OF PLANT BIOLOGY, 2003, 54 : 207 - 233
  • [3] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [4] Induction of genes encoding plastidic phosphorylase from spinach (Spinacia oleracea L) and potato (Solanum tuberosum L) by exogenously supplied carbohydrates in excised leaf discs
    Duwenig, E
    Steup, M
    Kossmann, J
    [J]. PLANTA, 1997, 203 (01) : 111 - 120
  • [5] DUWENIG E, 1996, THESIS U POTSDAM GER
  • [6] Potato plants exhibiting combined antisense repression of cytosolic and plastidial isoforms of phosphoglucomutase surprisingly approximate wild type with respect to the rate of starch synthesis
    Fernie, AR
    Swiedrych, A
    Tauberger, E
    Lytovchenko, A
    Trethewey, RN
    Willmitzer, L
    [J]. PLANT PHYSIOLOGY AND BIOCHEMISTRY, 2002, 40 (11) : 921 - 927
  • [7] Antisense repression of cytosolic phosphoglucomutase in potato (Solanum tuberosum) results in severe growth retardation, reduction in tuber number and altered carbon metabolism
    Fernie, AR
    Tauberger, E
    Lytovchenko, A
    Roessner, U
    Willmitzer, L
    Trethewey, RN
    [J]. PLANTA, 2002, 214 (04) : 510 - 520
  • [8] Sucrose to starch: a transition in molecular plant physiology
    Fernie, AR
    Willmitzer, L
    Trethewey, RN
    [J]. TRENDS IN PLANT SCIENCE, 2002, 7 (01) : 35 - 41
  • [9] Analysis of cytosolic heteroglycans from leaves of transgenic potato (Solanum tuberosum L.) plants that under- or overexpress the Pho 2 phosphorylase isozyme
    Fettke, J
    Poeste, S
    Eckermann, N
    Tiessen, A
    Pauly, M
    Geigenberger, P
    Steup, M
    [J]. PLANT AND CELL PHYSIOLOGY, 2005, 46 (12) : 1987 - 2004
  • [10] The glycan substrate of the cytosolic (Pho 2) phosphorylase isozyme from Pisum sativum L.:: identification, linkage analysis and subcellular localization
    Fettke, J
    Eckermann, N
    Poeste, S
    Pauly, M
    Steup, M
    [J]. PLANT JOURNAL, 2004, 39 (06) : 933 - 946