Pfister Barbara, Lu Kuan-Jen, Eicke Simona, Feil Regina, Lunn John E, Streb Sebastian, Zeeman Samuel C
Department of Biology, ETH Zurich, 8092 Zurich, Switzerland (B.P., K.-J.L., S.E., S.S., S.C.Z.); andMax Planck Institute for Molecular Plant Physiology, 14476 Potsdam, Germany (R.F., J.E.L.).
Department of Biology, ETH Zurich, 8092 Zurich, Switzerland (B.P., K.-J.L., S.E., S.S., S.C.Z.); andMax Planck Institute for Molecular Plant Physiology, 14476 Potsdam, Germany (R.F., J.E.L.)
Plant Physiol. 2014 Aug;165(4):1457-1474. doi: 10.1104/pp.114.241455. Epub 2014 Jun 25.
The major component of starch is the branched glucan amylopectin. Structural features of amylopectin, such as the branching pattern and the chain length distribution, are thought to be key factors that enable it to form semicrystalline starch granules. We varied both structural parameters by creating Arabidopsis (Arabidopsis thaliana) mutants lacking combinations of starch synthases (SSs) SS1, SS2, and SS3 (to vary chain lengths) and the debranching enzyme ISOAMYLASE1-ISOAMYLASE2 (ISA; to alter branching pattern). The isa mutant accumulates primarily phytoglycogen in leaf mesophyll cells, with only small amounts of starch in other cell types (epidermis and bundle sheath cells). This balance can be significantly shifted by mutating different SSs. Mutation of SS1 promoted starch synthesis, restoring granules in mesophyll cell plastids. Mutation of SS2 decreased starch synthesis, abolishing granules in epidermal and bundle sheath cells. Thus, the types of SSs present affect the crystallinity and thus the solubility of the glucans made, compensating for or compounding the effects of an aberrant branching pattern. Interestingly, ss2 mutant plants contained small amounts of phytoglycogen in addition to aberrant starch. Likewise, ss2ss3 plants contained phytoglycogen, but were almost devoid of glucan despite retaining other SS isoforms. Surprisingly, glucan production was restored in the ss2ss3isa triple mutants, indicating that SS activity in ss2ss3 per se is not limiting but that the isoamylase suppresses glucan accumulation. We conclude that loss of only SSs can cause phytoglycogen production. This is readily degraded by isoamylase and other enzymes so it does not accumulate and was previously unnoticed.
淀粉的主要成分是支链葡聚糖淀粉。淀粉的结构特征,如分支模式和链长分布,被认为是使其能够形成半结晶淀粉颗粒的关键因素。我们通过创建缺乏淀粉合酶(SSs)SS1、SS2和SS3组合(以改变链长)以及去分支酶异淀粉酶1-异淀粉酶2(ISA;以改变分支模式)的拟南芥(Arabidopsis thaliana)突变体,来改变这两个结构参数。isa突变体在叶肉细胞中主要积累植物糖原,在其他细胞类型(表皮和维管束鞘细胞)中只有少量淀粉。通过突变不同的SSs,这种平衡会发生显著变化。SS1突变促进淀粉合成,恢复叶肉细胞质体中的颗粒。SS2突变降低淀粉合成,消除表皮和维管束鞘细胞中的颗粒。因此,存在的SS类型会影响葡聚糖的结晶度,进而影响其溶解度,补偿或加剧异常分支模式的影响。有趣的是,ss2突变体植物除了异常淀粉外还含有少量植物糖原。同样,ss2ss3植物含有植物糖原,但尽管保留了其他SS同工型,几乎没有葡聚糖。令人惊讶的是,ss2ss3isa三重突变体中葡聚糖的产生得以恢复,这表明ss2ss3本身的SS活性并不受限,而是异淀粉酶抑制了葡聚糖的积累。我们得出结论,仅SSs的缺失会导致植物糖原的产生。它很容易被异淀粉酶和其他酶降解,所以不会积累,以前也未被注意到。