Cell Cycle Control in Arabidopsis

Although the basic mechanism of cell cycle control is conservedamong eukaryotes, its regulation differs in each type of organism.Plants have unique developmental features that distinguish themfrom other eukaryotes. These include the absence of cell migration,the formation of organs throughout the entire life-span fromspecialized regions called meristems, and the potency of non-dividingcells to re-enter the cell cycle. The study of plant cell cyclecontrol genes is expected to contribute to the understandingof these unique developmental phenomena. The principal regulatorsof the eukaryotic cell cycle, the cyclin-dependent kinases (CDKs)and cyclins, are conserved in plants. This review focuses oncell cycle regulation in the plant Arabidopsis thaliana . Whileexpression of one Arabidopsis CDK gene, Cdc2aAt, was positivelycorrelated with the competence of cells to divide, expressionof a mitotic-like cyclin, cyc1At, was almost exclusively confinedto dividing cells. The expression of the Arabidopsis -type cyclinsappears to be an early stage in the response of plant cellsto external and internal stimuli. Arabidopsis thaliana (L.) Heynh.; cell cycle; CDK; cyclin; plant development; plant hormone     

THE ENUMERATION OF FAECAL STREPTOCOCCI IN FOODS, USING PACKER'S CRYSTAL VIOLET SODIUM AZIDE BLOOD AGAR

SUMMARY: Packer's crystal violet sodium azide blood agar (Packer, 1943) used in poured plates at 36·1°, gave satisfactory recovery of pure cultures of Lancefield group D streptococci and completely inhibited the growth of 11 other species of aerobic and anaerobic food bacteria, including Strep. lactis (5 strains). Later, however, one group N streptococcus was obtained which did grow in Packer's agar at 36·1°. To eliminate this organism the incubation temperature had to be increased to 39·5°, using agar strips (Stirling et al. 1950) incubated in a water bath to secure strict temperature control. Under these conditions the recovery of typical group D streptococci was never consistently below 50% of the count in tryptone dextrose yeast extract agar at 31·1°.     

Factors affecting the Abscission of Reproductive Organs in Yellow Lupins (Lupinus luteus L.): I. THE EFFECT OF DIFFERENT PATTERNS OF FLOWER REMOVAL

1. The effect of various patterns of flower removal on pod settingwas investigated in Lupinus luteus L. Four-fifths, three-fifths,or two-fifths of the flowers of the main inflorescence wereremoved according to ten different patterns. 2. All flowers could produce pods but later ones were less efficientin doing so. Developing pods had an abscission-inducing effecton later flowers, which became increasingly effective towardsthe apical part of the inflorescence. More pods were retained when flowers on each consecutive whorlwere arranged in a spiral than when the same number was arrangedvertically. Pod setting was incomplete when the number of flowers per inflorescencewas reduced well below the total number of pods normally present. 3. The number of ovules in consecutive flowers gradually decreasedfrom an average of 5.7 at the base to 4.3 at the top of theinflorescence. The ratio of seeds to ovules fluctuated irregularlybetween 65 and 94 per cent, and did not indicate a general trendin embryo abortion. 4. The growth-rate of pods at the top of the inflorescence wasmuch slower than at the bottom. Vascular differentiation wasalmost absent at the top of the inflorescence when the flowerswere fertilized, and further vascular tissue was produced onlywhen flowers produced pods.