Peroxidase and polyphenol oxidase activity in malformed mango inflorescence caused byFusarium moniliforme var.subglutinans

Peroxidase and polyphenol oxidase activities in malformed mango inflorescences of ‘Himsagar’ and ‘Bombay green’ oultivars wore found to be increased considerably following infection byFusarium moniliforme var.subglutinans. Whether such increased activities were due to their synthesis by the pathogen or the host, or both, was not studied although it was found that the pathogen was incapable of producing the enzymesin vitro. The activities of both the enzymes in infected tissues were found to increase considerably during the experimental period. It was found that activities of polyphenol oxidase were inhibited in the presence of sodium diethyldithiocarbamate and phenylthiourea; the former acted as chelating agent of Cu of the enzymes and the latter as a competitive inhibitor. Similarly, peroxidase activity was found to be inhibited by cycloheximide which acted as inhibitor of enzyme protein synthesis. The fact that the ‘Himsagar’ cultivar showed greater enzyme activity than the ‘Bombay green’ cultivar possibly suggests its higher resistance to the pathogen.     

Constant rate allocation in nymphal development in species of Hemiptera

Abstract. This study investigated the existence of rate isomorphy (the constant allocation of relative times to different stages of development under different abiotic conditions) in Macrolophus pygmaeus (Hemiptera: Miridae; a phytophagous and predatory insect). Replicated data were used from a range of temperatures regarding (i) the developmental period of each nymphal stage in relation to the total duration of nymph development, when feeding on three host plants either with different prey species or without prey, and (ii) its egg, total nymphal and preoviposition period, on two host plants, with different prey species. The proportion of time required for the development of each nymphal stage of M. pygmaeus is not different among the temperatures or the kind of food available. These proportions ranged among the different host plants, temperatures and prey presence/absence from 17.3–21.8% in the first, 14.5–18.8% in the second, 14.2–18.3% in the third, 16.5–21.0% in the fourth and from 25.4–30.6% in the fifth nymphal stage. Thus, temperature does not significantly affect the proportion of time spent in each nymphal stage and rate isomorphy exists in nymphal development. This phenomenon was also investigated using data from the literature, and it also occurs in several other Hemiptera species. Therefore, there appears to be a constant time allocation in the nymphal development of the higher taxonomic groups of insects. However, for M. pygmaeus, rate isomorphy does not hold when considering egg‐to‐egg development and the relative duration of times to egg hatch, total nymphal development and preoviposition period. The ecophysiological implications of this rate isomorphy phenomenon are discussed in relation to endocrinological mechanisms. Apart from its theoretical interest, the existence of rate isomorphy simplifies studies on the rate of development and the estimation of thermal constants of an insect, which are essential for the prediction of insect population dynamics. It is also proposed that the term ‘rate isomorphy’ does not strictly describe the phenomenon, and it is suggested that ‘constant rate allocation’ would be a more suitable term.     

Degradation of 1,2-dichlorobenzene by a Pseudomonas sp

A Pseudomonas sp. that was capable of growth on 1,2-dichlorobenzene (o-DCB) or chlorobenzene as a sole source of carbon and energy was isolated by selective enrichment from activated sludge. The initial steps involved in the degradation of o-DCB were investigated by isolation of metabolites, respirometry, and assay of enzymes in cell extracts. Extracts of o-DCB-grown cells converted radiolabeled o-DCB to 3,4-dichloro-cis-1,2-dihydroxycyclohexa-3,5-diene (o-DCB dihydrodiol). 3,4-Dichlorocatechol and o-DCB dihydrodiol accumulated in culture fluids of cells exposed to o-DCB. The results suggest that o-DCB is initially converted by a dioxygenase to a dihydrodiol, which is converted to 3,4-dichlorocatechol by an NAD+-dependent dehydrogenase. Ring cleavage of 3,4-dichlorocatechol is by a catechol 1,2-oxygenase to form 2,3-dichloro-cis,cis-muconate. Preliminary results indicate that chloride is eliminated during subsequent lactonization of the 2,3-dichloro-cis,cis-muconate, followed by hydrolysis to form 5-chloromaleylacetic acid.     

Simultaneous biodegradation of chlorobenzene and toluene by a Pseudomonas strain

Pseudomonas sp. strain JS6 grows on a wide range of chloro- and methylaromatic substrates. The simultaneous degradation of these compounds is prevented in most previously studied isolates because the catabolic pathways are incompatible. The purpose of this study was to determine whether strain JS6 could degrade mixtures of chloro- and methyl-substituted aromatic compounds. Strain JS6 was maintained in a chemostat on a minimal medium with toluene or chlorobenzene as the sole carbon source, supplied via a syringe pump. Strain JS6 contained an active catechol 2,3-dioxygenase when grown in the presence of chloroaromatic compounds; however, in cell extracts, this enzyme was strongly inhibited by 3-chlorocatechol. When cells grown to steady state on toluene were exposed to 50% toluene-50% chlorobenzene, 3-chlorocatechol and 3-methylcatechol accumulated in the medium and the cell density decreased. After 3 h, the enzyme activities of the modified ortho ring fission pathway were induced, the metabolites disappeared, and the cell density returned to previous levels. In cell extracts, 3-methylcatechol was degraded by both catechol 1,2- and catechol 2,3-dioxygenase. Strain JS62, a catechol 2,3-dioxygenase mutant of JS6, grew on toluene, and ring cleavage of 3-methylcatechol was catalyzed by catechol 1,2-dioxygenase. The transient metabolite 2-methyllactone was identified in chlorobenzene-grown JS6 cultures exposed to toluene. These results indicate that strain JS6 can degrade mixtures of chloro- and methylaromatic compounds by means of a modified ortho ring fission pathway.