The Extent of Starch Turnover in Mature Pepper Leaves in the Light

The extent of starch turnover in pepper leaves in the lighthas been estimated. After leaves were labelled with ¹⁴CO₂ atconstant specific activity for 4–7 h, the irradiance wasreduced to a level which caused no net change in the starchcontent of the leaf, and the supply of ¹⁴CO₂ was removed. Therewas no significant change in specific activity of starch overthe following 6–10 h, thus there was no exchange of ¹⁴C-starchwith ¹²C-assimilates entering the chloroplasts. Starch, turnover, ¹⁴C-labelling, pepper, Capsicum annuum L.     

Ammonia Induces Starch Degradation in Chlorella Cells

When ammonia was added to cells of Chlorella which had fixed¹⁴CO₂ photo synthetically, ¹⁴C which had been incorporated intostarch was greatly decreased. A similar effect was observedwhen potassium nitrate and sodium nitrite were added. The ammonia-induceddecrease in ¹⁴C-starch was observed in all species of Chlorellatested. With cells of C. vulgaris 11h, most of the radioactivityin starch was recovered in sucrose, indicating that ammoniainduces the conversion of starch into sucrose. The percent of¹⁴C recovered in sucrose differed from species to species andpractically no recovery in sucrose was observed in C. pyrenoidosa.In most species tested, the enhancing effects of blue lightand ammonia on O₂ uptake as well as the ammonia effect on starchdegradation were greater in cells which had been starved inphosphate medium in the dark than in non-starved cells. In contrast,the enhancing effect of ammonia on dark CO₂ fixation was muchgreater in non-starved cells. C. pyrenoidosa was unique in thatblue light did not show any effect on its O₂ uptake. (Received August 15, 1984; Accepted November 16, 1984)     

A "Point of No Return" in the Cell Cycle of Chlorella

In a Chlorella culture growing synchronously at pH 6.3 undera 12 hr light/12 hr dark regime, DNA replication occurs betweenthe 8th and the 12th hour of the cycle, the main period of proteinand chlorophyll synthesis occurring between the 4th and 12thhour of the cycle. When the culture is transferred to alkalinepH at any time up to the 8 hr of the cycle, autospore releaseis prevented, and the pattern of synthesis of DNA, protein andchlorophyll is altered. However, when the culture is transferredto alkaline conditions after the 8th hour of the cycle, thepattern follows that of a culture growing at pH 6.3 with respectto cell number and volume, as well as protein, chlorophyll andDNA contents. Thus, a transition point seems to occur afterthe 8 hr of the cycle. The existence of such a point was alsodemonstrated by reciprocal experiments in which Chlorella wascultured at an alkaline pH and transferred to pH 6.3 at varioustimes in the cell cycle. ¹ Present address: Applied Research Institute, Ben-Gurion Universityof the Negev, P.O. Box 1025, Beer-Sheva 84110, Israel. (Received October 2, 1981; Accepted January 20, 1982)     

Starch Dissolution in Tobacco Leaves in the Light

Single attached leaves of tobacco, depleted of starch, wereallowed to assimilate a fixed amount of ¹⁴CO₂. About 50 percent. of the ¹⁴Carbon assimilated was translocated from thelamina concurrently with assimilation. Of that remaining inthe lamina 80 per cent. was incorporated into starch and sugar.Plants were then placed in air and continuous light of differentintensities as a means of controlling further starch synthesis.At about 500 f.c. there was no change in amount of starch after72 hours, but half the radioactivity was lost. At light intensitieslower than 500 f.c. percentage activity lost was greater thanthe percentage amount lost. In sunlight, where new starch synthesiswas very rapid, loss in activity from the radioactive portionwas prevented. In all circumstances activity virtually disappearedfrom both hexose and sucrose. It is concluded that starch dissolutionproceeded in light even when the amount was increasing. It isfurther suggested that the loss was mainly from outer layersof the starch grains which were replaced by newly synthesizedmaterial. Loss of sugar was by direct translocation rather thanpassage to starch, and complete replacement by new photosynthateoccurred in 24 hours.     

RNA metabolism in apices of Pharbitis nil daring floral induction

RNA metabolism was studied in apices of Pharbitis nil duringand after floral induction. In continuous light ³H-uridine accumulatedin RNA at a constant rate over an 18 hr period. In darkness,however, the rate of accumulation of label into RNA was constantuntil the 10th hour at which time a rapid burst of accumulationoccurred, peaking at the 14th hour of darkness and followedby a net loss of label. The RNA involved in this burst is probablymRNA due to its size and poly(A) content. This phenomenon doesnot seem to be associated with floral induction, since the siteof perception is the apex, and it also occurs under conditionswhere floral initiation is inhibited by a brief light interruptionof the dark period. Immediately after floral induction by a16-hr dark period the rate of RNA synthesis was suppressed about14%. This suppression lasts for about 12 hr and was followedby a twofold increase in the rate of RNA synthesis, comparedto non-induced apices, at 64 hr after the beginning of the inductivedark period. These post-induction changes were found to occurin all RNA fractions. ¹Present address: Department of Radiation Biology and Biophysics,University of Rochester School of Medicine and Dentistry, Rochester,N.Y. 14642, U.S.A. (Received March 15, 1976; )     

Effect of Temperature on Starch Degradation in Chlorella vulgaris 11h Cells

Analysis of products formed in Chlorella vulgaris 11 h cellsduring photosynthesis in air containing 3,000 ppm ¹⁴CO₂ at varioustemperatures revealed that the level of ¹⁴C-starch was maximumaround 20–24?C and decreased with further rise in temperatureuntil 40?C, while ¹⁴C-sucrose greatly increased at temperaturesabove about 28?C. Elevating the temperature from 20 to 38?Cduring photosynthetic ¹⁴CO₂ fixation resulted in a remarkabledecrease in ¹⁴C in starch and a concomitant increase in ¹⁴Cin sucrose. This conversion of starch to sucrose when shiftingthe temperature from 20 to 38?C proceeded even in the dark.Hydrolysis of sucrose by rß-fructosidase showed that,irrespective of the experimental conditions, the radioactivitiesin sucrose were equally distributed between glucose and fructose.The enhancement of starch degradation with temperature risewas more remarkable than that of the activity of ribulose bisphosphatecarboxylase from the same cells. When Chlorella cells whichhad been preloaded with ¹⁴C-starch after photosynthesis for30 min at 20?C were incubated in the dark for an additional30 min at 20?C, ¹⁴C-starch was degraded by only about 4%. However,the values after 30-min dark incubation at 28, 32, 36 and 40?Cwere increased by about 10, 19, 36 and 50%, respectively. Duringthe temperature-dependent conversion of starch to sucrose, nosignificant amount of radioactivity accumulated in free glucoseand maltose. (Received October 27, 1981; Accepted January 9, 1982)     

Changes in Steady-State Photosynthetic 14C-Incorporation into cellular Metabolites of Chlorellax pyrenoidosa during Transitions from High to Low Irradiance

Changes in the levels of ¹⁴C-labelled metabolites were monitoredin Chlorella pyrenoidosa cells during a transition from highto low irradiance, i.e., from 700 to 430 µmol quanta (400–700nm) m^–2 s^–1. Chlorella cells assimilated ¹⁴CO₂ photosynthetically(steady-state ¹⁴C-labelling) for 12 min at the high irradianceand then 10 min at the low irradiance. With the transition tolow light, the level of ¹⁴C-labelled ribulose 1,5- bisphosphate(RuBP) did not decrease, even though the rate of total ¹⁴C-incorporationdecreased by 80%. The data suggest that RuBP carboxylase deactivatesrapidly (within 1 or 2 min) on exposure to low light, causingRuBP pool sizes to be maintained (or even increased) in spiteof a decreased rate of RuBP regeneration. There was also evidenceof light modulation of other enzymes, including some enzymesinvolved in sucrose synthesis. The rate of sucrose synthesisdecreased with decrease in light intensity while the level ofuridine diphosphoglucose increased, but within a few minutes,both returned to their former levels. ¹Present address: Chemical Biodynamics, Lawrence Berkeley Laboratory,Building 3, 1 Cyclotron Road, Berkeley, CA 94720, U.S.A. (Received March 8, 1986; Accepted June 25, 1986)     

Export, Mobilization, and Respiration of Assimilates in Uniculm Barley during Light and Darkness

The respiratory losses and the pattern of carbon supply froma leaf of unicuim barley were examined during a complete diurnalperiod using a steady state ¹⁴C-labelling technique. After a delay of c. 1 h a portion of the ¹⁴C exported from acontinuously assimilating leaf was lost in respiration in thelight. This respiratory loss amounted to c. 20% of the total¹⁴C fixed. A further 28% of the total ¹⁴C fixed was respiredduring the dark period. In the light, carbon was fixed at a rate of c. 8·9 mgC dm^{–2 h–1} and exported from the leaf at ^c. 5·3mg C dm^{–2 h–1}. Dark export averaged ^c. 31% of theday-time rate. Carbohydrate was stored in the leaf during the day and was almostcompletely remobilized during the dark. Sucrose, the major reservecarbohydrate, was exported first whilst the starch level remainedconstant. After some 9 h of darkness, sucrose declined to alow level and starch remobilization began.     

Effect of the Photosynthetic Light Period on the Carbon Budget of Young Tomato Leaves

This study was carried out to elucidate the carbon budget inyoung tomato plants in photosynthetic light periods of 8, 12and 16 h after being acclimated to an 8-h light period. Thephotosynthetic rate was nearly constant for 16 h: thereforethe amount of ¹⁴C fixed was proportional to the light period(13·77 mg C per 8 h, 20·2 mg C per 12 h, 30·5mg C per 16 h). The amounts exported, lost by respiration and accumulated whenexpressed as percentages of the carbon fixed in the day differedlittle between the light periods. The leaf continued to exportcarbon at a nearly constant rate during the light periods and,for example, exported approximately twice as much during a 16-hperiod as in an 8-h light period, even though it was not acclimatedto the long light period. The amount of starch breakdown affected the amount of carbonexported and carbon lost by respiration at night, although itwas not sufficient to account for these losses altogether. Thepossible roles of carbon accumulation and respiration are alsodiscussed. Carbon budget, steady state feeding, ¹⁴C, photosynthesis, respiration, translocation, carbon metabolism, tomato, Lycopersicon esculentum Mill     

Effects of dark preincubation and chloramphenicol on blue light-induced CO2 incorporation in Chlorella cells

Chlorella cells incubated in the dark longer than 12 hr showedpronounced blue light-induced ¹⁴CO₂ fixation into aspartate,glutamate, malate and fumarate (blue light effect), whereasthose kept under continuous light showed only a slight bluelight effect, if any. 2) During dark incubation of Chlorellacells, phosphoenolpyruvate carboxylase activity and the capacityfor dark ¹⁴CO₂ fixation decreased significantly, whereas ribulose-1,5-diphosphatecarboxylase activity and the capacity for photosynthetic ¹⁴CO₂fixation (measured under illumination of white light at a highlight intensity) did not decrease. 3) In cells preincubatedin the dark, intracellular levels of phosphoenolpyruvate and3-phosphoglycerate determined during illumination with bluelight were practically equal to levels determined during illuminationwith red light. 4) The blue light effect was not observed incells incubated widi chloramphenicol, indicating that blue light-inducedprotein synthesis is involved in the mechanism of the effect. (Received April 9, 1971; )     

Mobilization of Starch and Essential Oil Biogenesis during Leaf Ontogeny of Lemongrass (Cymbopogon flexuosus Stapf.)

The levels of starch, soluble sugars, starch mobilizing enzymes(amylases and phosphorylase) and sodium [2-^I4C] acetate incorporationinto essential oil have been examined during leaf ontogeny oflemongrass (Cymbopogon flexuosus Stapf., cv. OD-19). The degradationof starch was predominantly amylolytic and ß-amylasewas the major enzyme involved. Its activity was quite high duringthe period of active leaf growth accompanying active accumulationof essential oil. The activities of a-amylase and phosphorylasewere relatively lower. The change in starch to soluble sugarsratio was inversely related to ß-amylase activity.The time-course (12 h light followed by 12 h dark) monitoringof the [^I4C]-radioactivity in starch and essential oil, afterexposure of the immature (15 days after emergence) leaf to ¹⁴CO₂,revealed a progressive loss of label from starch and a parallelincrease in radioactivity in essential oil. The results havebeen discussed in relation to degradation of transitory starchserving as the source of carbon precursor for essential oil(monoterpene) biogenesis in the tissue. The amount of exogenouslysupplied acetate incorporated into essential oil increased tremendouslywith 5-10 fold decrease in specific activity of the labelledacetate (2,110 GBq mole^–1). The effect was largely manifestedin ‘citral’, the chief (ca. 80%) constituent oflemongrass essential oil. Ontogenetically, the amount of essentialoil synthesized from the exogenously supplied precursor (acetate)was much higher in young (10 days after emergence) than in mature(30 days after emergence) leaf. Thus, the leaf developmentalphase influences the expression of essential oil metabolismand actual synthesis. Only young lemongrass leaves are substantiallyactive to synthesize essential oil. The oil biosynthetic phaseappears to be coordinated/integrated with the development ofelevated levels of certain primary metabolic activities likestarch mobilization. ¹CIMAP Publication No. 706 ²Present address: CSIR Complex, Palampur-176 061, Kangra Distt.Himachal Pradesh, India ^J Present address (until October 10, 1991): Department of Biology,Queen's University, Kingston, Ontario, K7L 3N6, Canada (Received November 30, 1990; Accepted May 31, 1991)     

Allocation of Photosynthate to Individual Tubers of Solanum tuberosum L.: I. RELATIONSHIP BETWEEN TUBER GROWTH RATE AND ENZYME ACTIVITIES OF THE STARCH METABOLISM

Potato plants (Solanum tuberosum L.) were grown in water culturein a controlled environment. Cooling (+8°C) of individualtubers decreased their growth rates and increased the growthrates of non-cooled tubers of the same plant. The carbohydrateconcentration in non-cooled and cooled tubers did not differsignificantly, but ¹⁴C-import from labelled photosynthate waslower in cooled than in non-cooled tubers. The markedly lowerconversion rate of ethanol-soluble ¹⁴C to starch in cooled,in comparison to non-cooled tubers, was not associated withsignificant differences in the in vitro activities of starchsynthase, ADPG-pyrophosphorylase and starch phosphorylase understandard assay conditions (+30°C). However, the Q₁₀-valuesof the enzymes differed in vitro in the temperature range between30°C and 8°C, leading to a marked decrease in the activityratio of ADPG-pyrophosphorylase/starch phosphorylase in cooledtubers. In tubers differing in growth rates without manipulation, 14d after tuber initiation significant positive correlations werefound between ¹⁴C-concentration of tuber tissue and the in vitroactivities of starch synthase and ADPG-pyrophosphorylase anda significant negative correlation between ¹⁴C-concentrationand starch phosphorylase. In contrast, in tubers which wereanalysed 5 d after initiation, there were only small differencesbetween tubers in growth rate, ¹⁴C import and the activity ratioADPG-pyrophosphorylase/starch phosphorylase. From various directand indirect evidence it is concluded that the growth rate ofindividual tubers, and thus the sink strength, is at least inpart controlled by the activity of starch synthesizing enzymes. Key words: Potato tuber, cooling, starch synthesizing enzymes     

The Distribution and Identity of Assimilates in Tomato with Special Reference to Stem Reserves

Much of the work on the distribution of ¹⁴C-labelled assimilatesin tomato has been done in winter under low light intensities,and consequently the reported distribution patterns of ¹⁴C maynot be representative of plants growing in high light. Further,there are several somewhat conflicting reports on patterns ofdistribution of ¹⁴C-assimilates in young tomato plants. We soughtto clarify the situation by studying the distribution of ¹⁴C-assimilatesin tomato plants of various ages grown in summer when the lightintensity was high. In addition, the role of the stem as a storageorgan for carbon was assessed by (a) identifying the chemicalfractions in the stem internode below a fed leaf and monitoring¹⁴ C activity in these fractions over a period of 49 d, and(b) measuring concentrations of unlabelled carbohydrates inthe stem over the life of the plant. The patterns of distribution of ¹⁴C-assimilates we found fortomato grown under high light intensity confirmed some of thosedescribed for plants grown under low light, but export of ¹⁴Cby fed leaves was generally higher than reported for much ofthe earlier work. Lower leaves of young plants exported over50% of the ¹⁴C they fixed, although export fell sharply as theplants aged. Initially, the roots and apical tuft were strongsinks for assimilates, but they had declined in importance bythe time plants reached the nine-leaf stage. On the other hand,the stem became progressively more important as a sink for ¹⁴C-assimilates.Older, lower leaves exported more of their ¹⁴C-assimilates tothe upper part of the plant than to the roots, whereas youngleaves near the top of the plant exported more of their assimilatesto the roots. The stem internode immediately below a fed leafhad about twice the ¹⁴C activity of the internode above theleaf. Mature leaves above and below a fed leaf rarely importedmuch ¹⁴C, even when in the correct phyllotactic relationshipto the fed leaf. In the first 3 d after feeding leaf 5 of nine-leaf plants, theorganic and amino acid pools and the neutral fraction of theinternode below the fed leaf had most of the ¹⁴C activity, butby 49 d after feeding, the ethanolic-insoluble, starch and lipidfractions had most of the ¹⁴C activity. Glucose, fructose andsucrose were the main sugars in the stem. Although concentrationsof these sugars and starch declined in the stem as the plantsmatured, there was little evidence to indicate their use infruit production. Stems of plants defoliated at the 44-leafstage had lower concentrations of sugars and starch at maturity,and produced less fruit than the controls. It was concludedthat tomato is sink rather than source limited with respectto carbon assimilates, and that the storage of carbon in thestem for a long period is possibly a residual perennial traitin tomato.Copyright 1994, 1999 Academic Press Lycopersicon esculentum, tomato, assimilate distribution, ¹⁴C, internode storage, sink-source relationships, starch, stem reserves, sugars     

Effect of Day Length and Night Temperature on Starch Accumulation and Degradation in Soybean

The effect of the day length on the accumulation and the degradationof the starch in leaf, stem and root tissues of prefloweringsoybean plants was determined by growing plants under a 7 or14 h light regime. As has been reported previously, the rateof starch accumulation by leaves was inversely related to daylength. High sucrose content was associated with a high rateof starch accumulation. Stem tissue showed diurnal fluctuationsin starch content and the rate of accumulation was also inverselyrelated to day length. This starch resulted from photosynthesiswithin the stem itself. A negligible amount of starch was foundin root tissue of both sets of plants. The rate of starch breakdown in leaves of 7 h plants was significantlyless than that in 14 h plants. Nevertheless, leaf starch inshort day length plants was depleted at least 4 h prior to theend of the dark period. In both sets of plants, degradationof stem starch started simultaneously with that in the leavesand continued throughout the dark period, although at a muchlower rate than that of leaves. Thus, stem starch acted as abuffer once leaf starch was depleted, providing carbohydratesto the plant, although in small quantities. To determine if soybean leaves adjust their rate of starch accumulationduring the light period to different dark period temperatures,plants were grown under temperature regimes of 30/20 ^°Cand 30/30 ^°C. Plants did not differ in rate of starch accumulationor CO₂ exchange rate, but did show large differences in growthcharacteristics. High temperature plants had significantly greaterleaf area and tended to have greater leaf area ratio. Thus,despite similar rates of starch accumulation on a leaf areabasis, high temperature plants accumulated greater amounts ofstarch on a per plant basis. Glycine max(L.)Merr., soybean reserve carbohydrates, remobilization, source-sink realtionships     

Light-Induced Changes in the Molecular Size of Starch in Colorless Chlorella Cells

Starch from colorless mutant cells of Chlorella vulgaris (#125), grown heterotrophically in the dark, was fractionatedby agarose gel chromatography. The molecular weight distributionof starch showed only one pronounced maximum at 2?10⁶ (L-starch).Exposure of cells to white light decreased significantly inthe amounts of the total starch and L-starch. This also wastrue under non-growth conditions, the same effect being foundto depend on blue light. The role of light on starch degradationis discussed. (Received November 29, 1984; Accepted February 25, 1985)     

Photosynthetic electron transport in Dunaliella tertiolecta (Chlorophyceae) measured by fast repetition rate fluorometry: relation to carbon assimilation

A comparison of photosynthesis-irradiance response curves (P–Eresponse curves) obtained through fast repetition rate (FRR)fluorometry and radiocarbon (¹⁴C) tracer method was made inthe chlorophyte, Dunaliella tertiolecta, grown under differentirradiance conditions. In FRR-based P–E response curveexperiments, actinic light provided by white light-emittingdiodes (LEDs) was increased gradually from 0 to 1500 µmolquanta m^–2 s^–1 and the rate of photosyntheticelectron transport was determined at each light level. Short-termexperiments (20 min) of ¹⁴C-based P–E response curvewere carried out with an improved photosynthetron, which containswhite LEDs as the light source. Irrespective of growth irradiance,the ratios of FRR to ¹⁴C-based initial slopes were almost uniform.The ratios of FRR- to ¹⁴C-based maximum rates were 25–36%higher than those of FRR- to ¹⁴C-based initial slopes. The relationshipbetween electron transport and carbon assimilation was non-linearwith increasing discrepancy towards high actinic light. Thisnon-linear relationship between FRR- and ¹⁴C-based estimatesis primarily due to the effect of physiological processes stimulatedat high levels of light, such as cyclic electron flow and theMehler reaction. The results of this study indicate that theFRR fluorometry can be used as a good indicator of photosyntheticrates from low to middle light levels, but becomes increasinglyquestionable as the maximum photosynthetic rate is approached.The degree to which this relationship is further affected bynutrient-status warrants investigation.     

Regulation of photosynthetic carbon metabolism in synchronously growing Chlorella pyrenoidosa

The physical properties and photosynthetic metabolism of synchronizedcells of Chlorella pyrenoidosa are described. Cells, synchronizedby successive periods of light and dark, photosynthesized understeady-state conditions for 30 min with ¹⁴CO₂. Pool sizes ofmetabolic intermediate compounds, and rates of flow of carbonthrough these pools, were determined. Cell properties and metabolismwere studied for cells just divided, at three periods duringthe growing stage, at the time of maximum DNA synthesis, justprior to division (after continuous light, and after 5 hr darkness),and following division after continuous light for 37 hr. Changes in pool sizes and flow rates are correlated with relativeshifts between amino acid and protein synthesis, which is greatestduring the growing period and DNA-synthesizing stage, and sucrosesynthesis, which is greatest in the divided cells (after darkness)and pre-division cells (after darkness). The effects of thestage of cell growth and of a prior period of darkness can beseparated to some extent by these studies, and in some respectsare additive. Specific sites of metabolic regulation discerned in these experimentsinclude the following: 1) Ribulose diphosphate carboxylase,2) fructose diphosphatase and sedoheptulose diphosphatase, 3)the synthesis of sucrose, probably at the reaction between fructose-6-phosphateand uridine diphosphoglucose to give sucrose phosphate and uridinediphosphate, 4) amino acid synthesis, at the level of nitratereduction, and 5) amino acid synthesis, at the level of carbonflow from the photosynthetic carbon reduction cycle to aminoacid carbon skeletons. (Received October 31, 1969; )     

ROLE OF NUCLEIC ACID AND PROTEIN METABOLISM IN THE INITIATION OF GROWTH AT GERMINATION

When dry decotyledonized embryos of Raphanus are supplied withwater, a brief period of water absorption (phase A) is followedby a period of no fresh weight increase (phase B) which lastsfor 8 hr at 30°. In this period, embryos become ready toadvance into the period of fresh weight increase (phase C). When embryos were exposed to various concentrations of thiouracilor actinomycin D solution from 0 hr of water supply, increasesin fresh weight and in RNA content measured at 13 hr were inhibitedin parallel with each other. Chloramphenicol and puromycin inhibitedthe fresh weight increase without affecting the RNA increase.When embryos were exposed to thiouracil or puromycin for 2,4 and 6 hr, beginning at 0 hr of water supply, the start ofphase C delayed 2, 4 and 6 hr, respectively. When these drugswere given after phase B had progressed at least for 2 hr, thedelay of the start of phase C was shorter than the period ofthe drug treatment. If given at the end of phase B, thiouraciland actinomycin D inhibited the incorporation of ¹⁴C-uracilbut not the fresh weight increase, while chloramphenicol andpuromycin inhibited the latter without inhibiting the former. During phase B, protein content per dry weight of embryo didnot increase, but the rate of ¹⁴C-leucine incorporation increasedremarkably to reach the level in phase C. Incorporation of labeledleucine was inhibited if embryos were subjected to thiouracilor actinomycin D action during phase B, but not if the drugswere given when phase B had been completed. Puromycin and chloramphenicolinhibited the incorporation whenever they were given. The increase in respiratory activity during phase B was inhibitedrelatively little by the above mentioned four drugs. In conclusion syntheses of RNA and protein seem to be essentialfor the progress of phases B and C, protein synthesis havinga more direct effect. (Received September 17, 1965; )     

Synthesis and Dissolution of Starch labelled with 14Carbon in Tobacco Leaf Tissue

Tobacco leaves depleted of starch, were detached and allowedto assimilate equal amounts of ¹⁴CO₂ and ¹²CO₂in succession,and vice versa. Distribution of radioactivity in starch, andsugars was determined after assimilation and after disks cutfrom the leaves had been kept in darkness for times up to 40hours. The amount and activity of the CO₂ was also determined.¹⁴C and ¹²C were incorporated in equal amounts into starch independentlyof the order in which they were supplied. In contrast sucrosehad high activity ¹⁴C was given last, and hexose a low one.The reverse was true when ¹²C was given last. Activity of respiratoryCO₂ was slightly higher when ¹⁴C was assimilated last as comparedwith ¹²C. In the dark only ¹⁴C or ¹²C was at first lost fromstarch, in accordance or removal of discrete layers. Analyticalresults show that starch is the main respiratory substrate andto account for the redistribution of radioactivity in passageto CO₂ it is concluded that sucrose occurs at two sites separatedinter-or intra-cellularly, one of which is in equilibrium withthe system intrconverting starch and CO₂ and at the other hexosesare produced by inversion. A starch-like polysaccharide is formedduring assimilation which persists in the dark and there isa significant contribution to respiration of carbon from non-carbohydratesources when leaf disks are kept on the dark.     

Studies on the Cell Wall of Chlorella IV. Incorporation of Glucose-Carbon into Cell Walls of Synchronously Growing Cells of Chlorella ellipsoidea

Uniformly ¹⁴C-labeIled glucose was fed to synchronously growingChlorella cells in the dark or in light. The rate of ¹⁴C-incorporationinto hemicellulose showed two maxima one in the growth phaseand one in the reproductive phase. Significant ¹⁴Cincorporationinto a "rigid wall" was found only in the reproductive phase. (Received April 14, 1983; Accepted June 15, 1983)