Molecular Biology Unit, Tata Institute of Fundamental Research, Bombay 400 005, India.
Plant Physiol. 1979 Jul;64(1):154-8. doi: 10.1104/pp.64.1.154.
In the growing chloronema cell suspension cultures of the moss Funaria hygrometrica Hedw., activities of several enzymes have been found to be cell-density-dependent. Cyclic nucleotide phosphodiesterase (cNPDE), nitrate reductase (NR), and protein kinase showed highest activity at a low cell density (1 to 2 milligrams per milliliter) while indoleacetic acid (IAA) oxidase and peroxidase were highest at a high cell density (>10 milligrams per milliliter). 3'-Nucleotidase and the glycolytic enzymes (aldolase, hexokinase, phosphofructokinase, phosphoglucoisomerase, pyruvate kinase, and triose phosphate isomerase) showed no significant dependence on the cell density. Alternatively, if the NR and peroxidase activities were determined as a function of time in batch cultures, their levels were maximal 60 to 70 and 320 hours after subculture, respectively, the corresponding cell densities being 1 to 2 and 23 milligrams per milliliter. The relationship between cell density and NR and peroxidase activities is the same, whether these enzymes are measured in batch cultures during a growth cycle or in the cells cultured at different initial inoculum densities for a constant time. Conventionally enzymic changes have been correlated with growth phases; however, it is felt that the pattern of enzymic activities can also be interpreted as cell-density-dependent.In moss protonema, the dependence of cNPDE, IAA oxidase, and peroxidase on cell density may play an important role in modulating the endogenous levels of IAA and cAMP, both of which regulate the differentiation of specific cell types (Johri and Desai 1973 Nature New Biol 245: 223-224; and Handa and Johri 1976 Nature 259: 480-482).
在湿地藓(Funaria hygrometrica Hedw.)的不断生长的绿藻体悬浮培养物中,人们发现几种酶的活性与细胞密度有关。环核苷酸磷酸二酯酶(cNPDE)、硝酸还原酶(NR)和蛋白激酶在低细胞密度(1 至 2 毫克/毫升)下表现出最高的活性,而吲哚乙酸(IAA)氧化酶和过氧化物酶在高细胞密度(>10 毫克/毫升)下表现出最高的活性。3'-核苷酸酶和糖酵解酶(醛缩酶、己糖激酶、磷酸果糖激酶、磷酸葡萄糖异构酶、丙酮酸激酶和磷酸丙糖异构酶)没有明显依赖于细胞密度。或者,如果将 NR 和过氧化物酶的活性作为分批培养物中时间的函数来测定,它们的水平在继代培养后分别达到 60 至 70 小时和 320 小时的最大值,相应的细胞密度分别为 1 至 2 毫克/毫升和 23 毫克/毫升。无论在生长周期中分批培养物中测定这些酶,还是在不同初始接种密度下培养细胞恒定时间,细胞密度与 NR 和过氧化物酶活性之间的关系是相同的。传统上,酶的变化与生长阶段有关;然而,人们认为酶活性的模式也可以解释为细胞密度依赖性。在藓原丝体中,cNPDE、IAA 氧化酶和过氧化物酶对细胞密度的依赖性可能在调节内源性 IAA 和 cAMP 水平方面发挥重要作用,这两者都调节特定细胞类型的分化(Johri 和 Desai 1973 年《自然新生物学》245:223-224;以及 Hand 和 Johri 1976 年《自然》259:480-482)。