Dyer J. H., Ryu S. B., Wang X.
Department of Biochemistry, Kansas State University, Manhattan, Kansas 66506.
Plant Physiol. 1994 Jun;105(2):715-724. doi: 10.1104/pp.105.2.715.
Multiple molecular forms of phospholipase D (PLD; EC 3.1.4.4) were identified and partially characterized in endosperm of germinated seeds and leaves of castor bean (Ricinus communis L. var Hale). The different PLD forms were resolved by nondenaturing polyacrylamide gel electrophoresis, isoelectric focusing, and size-exclusion chromatography. PLD was detected with both a PLD activity assay and immunoblots with PLD-specific antibodies. There were three major forms of PLD, designated types 1, 2, and 3, based on their mobility during nondenaturing polyacrylamide gel electrophoresis. Molecular masses of the PLD variants were estimated at 330, 230, and 270 kD for the types 1, 2, and 3, respectively. Isoelectric points of the native type 1, 2, and 3 PLDs were approximately 6.2, 4.9, and 4.8. Under the in vitro assay conditions used, the three forms of PLD exhibited the same substrate specificity, hydrolyzing phosphatidylcholine (PC), phosphatidylethanolamine (PE), and phosphatidylglycerol (PG) but not phosphatidylserine (PS) and phosphatidylinositol (PI). The three forms of PLD differed in their substrate preferences, and the order of activities was: PLD 1, PE > PG = PC; PLD 2, PE > PG > PC; PLD 3, PE = PG = PC. The Km values of PLDs 1, 2, and 3 for PC were 1.92, 2.62, and 5.18 mM, respectively. These PLDs were expressed differentially following seed germination and during leaf development. Type 1 was found in the early stages of seedling growth and in young leaves, type 2 was present in all the tissues and growth stages examined, and type 3 was expressed in senescent tissues. The PLDs shifted from largely cytosolic to predominantly membrane-associated forms during leaf development. The present studies demonstrate the structural heterogeneity of plant PLD and growth stage-specific expression of different molecular forms. The possible role for the occurrence of multiple molecular forms of PLD in cellular metabolism is discussed.
在蓖麻(Ricinus communis L. var Hale)萌发种子的胚乳和叶片中,鉴定出了磷脂酶D(PLD;EC 3.1.4.4)的多种分子形式,并对其进行了部分特性分析。通过非变性聚丙烯酰胺凝胶电泳、等电聚焦和尺寸排阻色谱法分离出了不同的PLD形式。采用PLD活性测定法和PLD特异性抗体免疫印迹法检测PLD。基于它们在非变性聚丙烯酰胺凝胶电泳中的迁移率,有三种主要的PLD形式,分别命名为1型、2型和3型。PLD变体的分子量估计分别为1型330 kD、2型230 kD和3型270 kD。天然1型、2型和3型PLD的等电点分别约为6.2、4.9和4.8。在所使用的体外测定条件下,三种形式的PLD表现出相同的底物特异性,可水解磷脂酰胆碱(PC)、磷脂酰乙醇胺(PE)和磷脂酰甘油(PG),但不能水解磷脂酰丝氨酸(PS)和磷脂酰肌醇(PI)。三种形式的PLD在底物偏好上有所不同,活性顺序为:PLD 1,PE>PG = PC;PLD 2,PE>PG>PC;PLD 3,PE = PG = PC。PLD 1、2和3对PC的Km值分别为1.92、2.62和5.18 mM。这些PLD在种子萌发后和叶片发育过程中差异表达。1型在幼苗生长早期和幼叶中发现,2型存在于所有检测的组织和生长阶段,3型在衰老组织中表达。在叶片发育过程中,PLD从主要存在于细胞质中转变为主要与膜相关的形式。本研究证明了植物PLD的结构异质性以及不同分子形式的生长阶段特异性表达。讨论了PLD多种分子形式在细胞代谢中出现的可能作用。