ALBERT

Notes: Broccoli is well recognized as a source of glucosinolates and their isothiocyanate breakdown products. Glucoraphanin is one of the most abundant glucosinolates present in broccoli and its cognate isothiocyanate is sulphoraphane, a potent inducer of mammalian detoxication (phase 2) enzyme activity and anti-cancer agent. This study was designed to measure: glucosinolate levels in broccoli florets from an array of genotypes grown in several environments; the elevation of a key phase 2 enzyme, quinone reductase, in mammalian cells exposed to floret extracts; and total broccoli head content. There were significant environmental and genotype-by-environment effects on levels of glucoraphanin and quinone reductase induction potential of broccoli heads; however, the effect of genotype was greater than that of environmental factors. The relative rankings among genotypes for glucoraphanin and quinone reductase induction potential changed, when expressed on a per head basis, rather than on a concentration basis. Correlations of trait means in one environment vs. means from a second were stronger for glucoraphanin and quinone reductase induction potential on a per head basis than on a fresh weight concentration basis. Results of this study indicate that development of a broccoli phenotype with a dense head and a high concentration of glucoraphanin to deliver maximum chemoprotective potential (high enzyme induction potential/glucoraphanin content) is a feasible goal.

Notes: Biological damage to plants is commonly found from the Devonian but occurs most commonly from the Cretaceous. Damage inflicted on plants whilst they were alive may trigger a pathological response involving the growth of abnormal tissues. Much of the damage is caused by arthropods, particularly insects. Whilst some damage is non-taxon specific, such as simple feeding traces, other damage, such as leaf mines, galls or bark boring, may reveal the co-evolution of host specific taxa and the timing of such interactions. Damaged plants, particularly from the Cretaceous and Tertiary are described and illustrated. The geological history of the evolution of insect-related plant damage is briefly reviewed. Increased variety in the pathological response of plants is seen from the Cretaceous with the evolution of the angiosperms and diversification of numerous insect groups.

Notes: The effect of aerobic mesophilic microfloral concentration on the isolation of Listeria monocytogenes LM82 was studied in 31 (18 cheeses and 7 noncheese) retail foods having standard plate counts of 101 to 108 colony forming units (CFU)/g. Foods were spiked with L. monocytogenes and enriched at 30°C for 24 h in a selective enrichment broth used in a U.S. Food and Drug Administration method. Inoculum levels for isolation on modified McBride agar ranged from 0.1 to 〉 5 × 103 with a geometric mean value of 5 inoculated CFU/g or 1.4 CFU/g. Pure Enterococcus (Streptococcus) faecalis (0 to 6 × 106 inoculated CFU/mL) in the absence of food matrix had no effect on the enrichment of L. monocytogenes. Ease of isolation of LM82 was independent of the food microflora concentration both generally and in the specific food type of 9 Brie cheeses. Competition, when it occurs, therefore, may be due to specific bacterial competitors rather than bacterial numbers.

Notes: The effects of mycorrhizal infection, soil P availability and fruit production on the male function of reproduction were examined in two cultivars of tomato (Lycopersicon esculentum Mill.). Tomato plants were grown in a greenhouse under three treatment combinations: non-mycorrhizal, low P (NMPO); non-mycorrhizal, high P (NMP3); and mycorrhizal, low P (MPO). In addition, all treatment combinations were grown both with and without fruit. Fruit production decreased final leaf biomass, flower production and in vitro pollen tube growth rates, often reducing the beneficial effects of increased P uptake. Thus, fruit production diverted resources from subsequent vegetative growth, flower production and pollen development. As the growing season progressed, mean pollen production per flower and in vitro germination and tube growth decreased. Mycorrhizal infection and high soil P conditions increased final leaf biomass, flower production, mean pollen production per flower (in one cultivar) and in vitro pollen tube growth rates. Thus, mycorrhizal infection and high soil P conditions increased pollen quantity and quality, thereby enhancing fitness through the male function. Similar trends in these treatments suggested that mycorrhizal effects on the male function were largely the result of improved P acquisition.

Notes: Classical Mendelian experiments were conducted to determine the genetics and inheritance of quinclorac and acetolactate synthase (ALS)-inhibitor resistance in a biotype of Galium spurium. Plants were screened with the formulated product of either quinclorac or the ALS-inhibitor, thifensulfuron, at the field dose of 125 or 6 g active ingredient (a.i.) ha−1 respectively. Segregation in the F2 generation indicated that quinclorac resistance was a single, recessive nuclear trait, based on a 1 : 3 segregation ratio [resistant : susceptible (R : S)]. Resistance to ALS inhibitors was due to a single, dominant nuclear trait, segregating in the F2 generation in a 3 : 1 ratio (R : S). The genetic models were confirmed by herbicide screens of F1 and backcrosses between the F1 and the S parent. F2 plants that survived quinclorac treatment set seed and the resulting F3 progeny were screened with either herbicide. Quinclorac-treated F3 plants segregated in a 1 : 0 ratio (R : S), hence F2 progenitors were homozygous for quinclorac resistance. In contrast, F3 progeny segregated into three ratios: 1 : 0, 3 : 1 and 0 : 1 (R : S) in response to ALS-inhibitor treatment. This segregation pattern indicates that their F2 parents were either homozygous or heterozygous for ALS-inhibitor resistance. Therefore, there were clearly two distinct resistance mechanisms encoded by two genes that were not tightly linked as demonstrated by segregation patterns of the F3.

Notes: The effect of five herbicide safeners on preventing maize (Zea mays L.) injury by acetochlor [N-(2-ethyl-6-methyl-phenyl)-N-(ethoxymethyl)-chloroacetamide], their influence on herbicide uptake and metabolism to a glutathione (GSH) conjugate as well as on GSH content and glutathione S-transferase activity (GST) in untreated and herbicide with/without safener-pre-treated 4-day-old seedlings were determined. The safeners studied were: AD-67 (N-di-chloroacetyl-1-oxa-4-azaspiro-4-5-decane), BAS-145138 [1-dichloroacetyl-hexahydro-3,3,8a-trimethyl-pyrrolo(l,2-a)pyrimidin-6(2H)-one], dichlormid (N, A,-diallyl-2,2-dichlo-roacetamide), DKA-24 (N, N2-diallyl-N2dichloroacetylglycineamide) and MG-191 (2-dichloromethyl-2-methyl-1,3-dioxolane). All safeners significantly increased [14C]acetochlor uptake and metabolism rate, maize GSH content and GST activity. Seedlings receiving BAS-145138 pre-treatment metabolized almost 70% of the absorbed [14C]acetochlor within 10 min.Safener-enhanced GST activity was always found to be higher when [14C]acetochlor was used as the substrate compared with CDNB (1-chloro-2,4-dinitrobenzene). Although DKA-24 had a significantly lower influence on both herbicide metabolism and GST activity, it was nearly as effective a safener as BAS-145138, while the others provided no or poor protection to maize from acetochlor injury when they were not incorporated in the soil. Effets d'antidotes sur la toxicité, la pénétration et le métabolisme de I'acétochlore chez le mats etsur l'activité glutathion S-transférase Cinq antidotes d'herbicides diminuaient la toxicité de 1'acétochlore [N-(2-éthyl-6-méthyl-phényl)-N-(éthoxyméthyl)-chloroacétamide] à I'égard du maïs (Zea mays L.). Lew effet sur l'absorption de l'herbicide et sur son métabolisme en un conjugué avec le glutathion (GSH), de même que leur effet sur la teneur en GSH et 1'activité glutathion 5-transférase (GST) ont étéétudiés sur des maïs âgés de 4 jours. Les antidotes étaient: l'AD-67 (N-dichloroacétyl-1-oxa-4-azaspiro-4,5-décane), le BAS-145138 [1 -dichloroacétyl-hexahydro-3,3,8a-triméthyl-pyrrolo(l,2-a) pyrimidine-6(2H)-one], le di-chlormide (N, N-diallyl-2,2-dichloracétamide), le DKA-24 (N, N2-diallyl-N2-dichloracétylgly-cineamide] et le MG-191 (2-dichlorométhyl-2-méthyl-l,3-dioxolane). Tous les antidotes augmentaient de manière significative 1'absorption et le métabolisme de I'acétochlore 14C, ainsi que la teneur du maïs en GSH et son activité GST. Les jeunes plantes prétraitées avec le BAS-145138 métabolisaient en 10 min près de 70% de I'acétochlore 14C absorbé. L'activité GST stimulée par 1'antidote était toujours plus élevée avec I'acétochlore 14C comme substrat qu'avec le CDNB (1-chloro-2,4-dinitrobenzène).Le DKA-24 avait un effet significativement plus faible que le BAS-145138 sur le métabolisme de l'herbicide et sur l'activité GSH, mais son action antidote était presque aussi importante. Les autres produits n'apportaient au maïs qu'une protection faible ou nulle contre l'acétochlore quand ils n'étaient pas incorporés au sol. Wirkung von Safenern auf die Phytotoxizität, Aufnahme und Metabolismus von Acetochlor und die Glutathion-S-Transferase-Aktivität in Mais Die Wirkung von 5 Safenern (AD-67, BAS-145138, Dichlormid, DKA-24 und MG-191; chemische Bezeichnungen s.o.) auf die Phytotoxizität von Acetochlor für Mais (Zea mays L.) und ihr Einfluß auf die Aufnahme des Herbizids und Metabolismus zu einem Glutathion-(GSH-) Konjugat und auf die Glutathion-S-Transferase-(GST-)Aktivität wurde an 4 Tage alten Keimpflanzen untersucht. Durch die Vorbehandlung mit den Safenern wurden die [14C]-Acetochlor-Aufnahme- und -Metabolierungsrate, der GSH-Gehalt und die GST-Ak-tivität signifikant erhöht. Mit BAS-145138 vorbehandelte Keimpflanzen metabolisierten fast 70% des absorbierten [14C]-Acetochlor innerhalb von 10 min. Die durch die Safener erhöhte GST-Aktivität bei [14C]-Acetochlor als Substrat war im Vergleich zu Chlordinitroben-zen immer höher. Obwohl DKA-24 einen signifikant geringeren Einfluß sowohl auf den Herbizidmetabolismus als auch auf die GST-Aktivität hatte, war es fast so wirkungsvoll wie BAS-145138, während die anderen ohne Einarbeitung in den Boden für den Mais keinen oder geringen Schutz gegen Schäden durch Acetochlor boten.

Notes: Spo0A~P is the essential response regulator and transcription factor for sporulation initiation in Bacillus subtilis. The phosphorylation level of Spo0A in the cell is determined by the sensor kinase activity of the phosphorelay, donating phosphoryl groups, and the antagonistic effects of dephosphorylation mediated by the Rap and Spo0E families of phosphatases. In this study, spo0A mutations were generated that encoded proteins less sensitive to the activity of Spo0E than the wild-type protein. The Spo0A substitutions N12K, P60S, L62P and F88L are surface exposed and localize to the same face of the molecule as the active site and in its close proximity on the β1–α1, β3–α3 and β4–α4 loops. The corresponding surface in the Spo0F response regulator was shown previously to be involved in the interaction with the RapB phosphatase, as well as the KinA histidine kinase and the Spo0B phosphotransferase. Thus, residues occupying the same position (N12:Q12, F88:Y84) and the same loops in Spo0A or Spo0F are involved in the interaction with the structurally unrelated Spo0E and RapB phosphatases, respectively, in addition to kinases and phosphotransferase. The specificity in phosphatase target recognition must be the result of side-chain variability within the response regulators and the interactions they promote. The residues involved in Spo0E interaction are identical in all Spo0A orthologues from spore-forming Bacilli encoding Spo0E phosphatases.