We studied the impact of delayed leaf senescence on the functioning of plants growing under conditions of nitrogen remobilization. Interactions between cytokinin metabolism, Rubisco and protein levels, photosynthesis and plant nitrogen partitioning were studied in transgenic tobacco (Nicotiana tabacum L.) plants showing delayed leaf senescence through a novel type of enhanced cytokinin syn‐thesis, i.e. targeted to senescing leaves and negatively auto‐regulated (PSAG12–IPT), thus preventing developmental abnormalities. Plants were grown with growth‐limiting nitrogen supply. Compared to the wild‐type, endogenous levels of free zeatin (Z)‐ and Z riboside (ZR)‐type cytokinins were increased up to 15‐fold (total ZR up to 100‐fold) in senescing leaves, and twofold in younger leaves of PSAG12–IPT. In these plants, the senescence‐associated declines in N, protein and Rubisco levels and photosynthesis rates were delayed. Senescing leaves accumulated more (15N‐labelled) N than younger leaves, associated with reduced shoot N accumulation (–60%) and a partially inverted canopy N profile in PSAG12–IPT plants. While root N accumulation was not affected, N translocation to non‐senescing leaves was progressively reduced. We discuss potential consequences of these modified sink–source relations, associated with delayed leaf senescence, for plant productivity and the efficiency of utilization of light and minerals.
An ipt gene under control of the senescence-specific SAG12 promoter from Arabidopsis (P SAG12-IPT) significantly delayed developmental and postharvest leaf senescence in mature heads of transgenic lettuce (Lactuca sativa L. cv Evola) homozygous for the transgene. Apart from retardation of leaf senescence, mature, 60-d-old plants exhibited normal morphology with no significant differences in head diameter or fresh weight of leaves and roots. Induction of senescence by nitrogen starvation rapidly reduced total nitrogen, nitrate, and growth of transgenic and azygous (control) plants, but chlorophyll was retained in the lower (outer) leaves of transgenic plants. Harvested P SAG12-IPT heads also retained chlorophyll in their lower leaves. During later development (bolting and preflowering) of transgenic plants, the decrease in chlorophyll, total protein, and Rubisco content in leaves was abolished, resulting in a uniform distribution of these components throughout the plants. Homozygous P SAG12-IPT lettuce plants showed a slight delay in bolting (4-6 d), a severe delay in flowering (4-8 weeks), and premature senescence of their upper leaves. These changes correlated with significantly elevated concentrations of cytokinin and hexoses in the upper leaves of transgenic plants during later stages of development, implicating a relationship between cytokinin and hexose concentrations in senescence.
In a study of six potato varieties (Solanum tuberosum L.),
which were grown under two different
fertilization regimes, the biochemical potential of tuber tissue to
synthesize blackspot pigments
was distinguished from the actual blackspot susceptibility exhibited
after impact application.
Blackspot susceptibility and biochemical potential for pigment
synthesis were not correlated, which
supports the hypothesis that the extent to which the blackspot
potential is actually being used is
mediated by the sensitivity to cell decompartmentation.
Quantification of polyphenol oxidase (PPO),
soluble protein, and endogenous PPO substrates demonstrated that the
content of free tyrosine is
the predominant determinant for the biochemical potential for blackspot
synthesis. PPO was not
a limiting factor for pigment synthesis, even if PPO content was
relatively low. It was therefore
concluded that manipulation of PPO activity may offer a solution to the
problem of blackspot
formation only if it leads to a virtually complete elimination of PPO
activity.
Keywords: Solanum tuberosum L.; Solanaceae; potato; blackspot;
bruise; melanin; tyrosine;
chlorogenic acid; caffeic acid; polyphenol oxidase; enzymic
browning
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