Catalase from larvae of the camel tick Hyalomma dromedarii

Catalase plays a major role in protecting cells against toxic reactive oxygen species. Here, Catalase was purified from larvae of the camel tick Hyalomma dromedarii and designated TLCAT. It was purified by ammonium sulfate precipitation and chromatography on DEAE-cellulose, Sephacryl S-300 and CM-cellulose columns. Gel filtration and SDS-PAGE of the purified TLCAT indicated that the protein has a native molecular weight of 120 kDa and is most likely a homodimer with a subunit of approximately 60 kDa. The Km value of TLCAT is 12 mM H₂O₂ and displayed its optimum activity at pH 7.2. CaCl₂, MgCl₂, MnCl₂ and NiCl₂ increased the activity of TLCAT, while FeCl_2, CoCl₂, CuCl₂ and ZnCl₂ inhibited the activity of TLCAT. Sodium azide inhibited TLCAT competitively with a Ki value of 0.28 mM. The presence of TLCAT in cells may play a role in protecting H. dromedarii ticks against oxidative damage. This finding will contribute to our understanding of the physiology of these ectoparasites and the development of untraditional methods to control them.     

Enzymatic hydrolysis of rice straw and corn stalks for monosugars production

Rice straw and corn stalks were used as fermentation substrate for the evaluation of cellulases activity secreted by different organisms. The substrates were pretreated with alkaline hydrogen peroxide (AHP) for 6 h at 30 and 60 °C. From the fermentation studies, rice straw and corn stalks substrates showed the highest cellulases activity after 96 h at 60 °C of pre-treatment.     

Effect of long-term cold storage of the predatory mite Neoseiulus californicus at high relative humidity on post-storage biological traits

The present study investigated whether long-term cold storage at high relative humidity (RH) affected the quality of the predatory mite Neoseiulus californicus (McGregor) (Acari: Phytoseiidae) in terms of its survival and reproduction. For this purpose, we examined biological traits at the end of storage and during the post-storage period. Mated females three?days after adult emergence were stored individually in 1.5-ml vials for 15, 30, 45, 60, or 75?days at 5.0?±?0.3°C and RH of 99?±?0.1% under continuous darkness. At the end of the storage period, 94–100% of females had survived when the storage period was ≤30?days, but percent survival decreased with longer storage. After storage, female survival and oviposition rates were equivalent to un-stored females at 24?±?1°C, RH of 93?±?2%, and a photoperiod of LD 16:8?h. The quality of progeny (hatchability, survival to adulthood, and sex ratio) of stored females was not affected by storage periods as long as 60?days. These results indicate that storage using the tested method can preserve N. californicus for at least 30?days without any degradation.     

Factor Xa (FXa) inhibitor from the nymphs of the camel tick Hyalomma dromedarii

An inhibitor of factor Xa (FXa) was isolated from the nymphs of the camel tick Hyalomma dromedarii by a combination of chromatography on DEAE-cellulose and Sephacryl S-300 columns. The isolated nymphal FXa inhibitor turned out to be a homogenous preparation of a single polypeptide chain (15 kDa) as judged by both the native and denatured SDS-PAGE. Its pI value ranged from 7.7 to 7.9. The inhibitor is a potent anticoagulant since it prolonged both the activated partial thromboplastin time (APTT) and the prothrombin time (PT) of the camel plasma in a concentration-dependent manner. Its activity was threefold lower toward thrombin than FXa, but it did not inhibit any of the proteases; trypsin, α-chymotrypsin, papain, pepsin and subtilisin. The inhibitor binds at two sites on FXa uncompetitively with an inhibition constant (K_i) value of 134 nM.     

Peroxidases of Solanum melongena leaves

Three major peroxidases, designated as A, B₂ and B₂ from Solanum melongena leaves have been reported. Peroxidases-A, -B₂ and -B₂ were considered to be true peroxidases on the basis of k₁:k₄ ratio. The pH optima for the three enzymes were found to be 7·0, 6·0 and 6.0 respectively. These peroxidases differ in their k₁:k₄ ratio, in the effect of pH on this ratio and in the uric acid/guaiacol and o-dianisidine/guaiacol activity ratio.     

Purification and characterization of two glutathione peroxidases from embryo of the camel tick <Emphasis Type="Italic">Hyalomma dromedarii</Emphasis>

Two glutathione peroxidase isoenzymes were purified from 24-day old embryos of the camel tick Hyalomma dromedarii and designated tick embryo glutathione peroxidase 1 and 2 (TEGPx1 and TEGPx2). The purification procedure involved ammonium sulfate precipitation, as well as ion exchange and gel filtration column chromatography. Glutathione peroxidase isoenzymes subunit molecular mass was determined by SDS-PAGE to be 36 ± 2 kDa and 59 ± 1.5 kDa for TEGPx1 and TEGPx2, respectively. TEGPx1 isoenzyme exhibited a dimeric structure with native molecular mass of 72 kDa while TEGPx2 was a monomeric protein. TEGPx1 and TEGPx2 displayed their pH optima at 7.6 and 8.2. Both isoenzymes cleaved preferentially H₂O₂ with K _m values of 24 and 49 μM. Iodoacetamide competitively inhibited TEGPx1 with K _i value of 0.45 mM and 1.10; phenanthroline competitively inhibited TEGPx2 with K _i value of 0.12 mM. These results indicate the presence of two different forms of glutathione peroxidase in the developing camel tick embryos. This finding enhances our knowledge and understanding of the physiology of these ectoparasites and will encourage the development of new and untraditional control methods.     

Dispersal of diapausing Tetranychus urticae and T. kanzawai

The spider mites Tetranychus urticae Koch and Tetranychus kanzawai Kishida (Acari: Tetranychidae) overwinter mostly as mated adult diapausing females. Their overwintering survival depends in part on their dispersal towards suitable habitats. We investigated the dispersal behaviour of diapausing females of T. urticae and T. kanzawai with respect to factors known to affect the dispersal of non‐diapausing mites: light, population density, gravity, and humidity. In general, diapausing females of T. urticae showed a stronger tendency to disperse than did those of T. kanzawai under all test conditions. High population density promoted the dispersal of diapausing T. urticae, but not of T. kanzawai. Dispersal of diapausing females of both species was not significantly affected by gravity, humidity, or whether feeding damage was caused by conspecifics or heterospecifics. On plants, more T. urticae than T. kanzawai moved downward. We propose that dispersal after the onset of diapause may be an important life‐history strategy in T. urticae, but not in T. kanzawai.     

Effect of photoperiod on immature development and diapause induction in the Kanzawa spider mite, <Emphasis Type="Italic">Tetranychus kanzawai</Emphasis> (Acari: Tetranychidae)

The diapause response of the Kanzawa spider mite (KSM), Tetranychus kanzawai, was examined. KSMs were reared in aluminum bottles at 18°C with different combinations of light and dark periods created by the light-control unit. The developmental periods for all immature stages tended to decrease as the light period increased. The photoperiodic response curve for diapause induction showed that the critical (=50% diapause) light period was around 13 h days⁻¹. No diapause induction was observed when the light period was longer than 13.5 h days⁻¹ or under continuous light. At 13-h days⁻¹ light period, the developmental period for deutonymphal stage as well as for the total immature stages was longer in diapaused females than in non-diapaused females. These results indicate that immature development as well as diapause induction are affected by photoperiod and further suggest that diapause-inducing stimuli prolong the developmental period especially for the deutonymphal stage of KSMs.     

Rapid cold hardening response in the predatory mite Neoseiulus californicus

We investigated the rapid cold hardening (RCH) response in the predatory mite Neoseiulus californicus (McGregor) (Acari: Phytoseiidae). On direct exposure, ≤2 % of adult females survived ?10 °C for 2 h. However, when acclimatized first at 5 °C for 1 h, 75 % of females survived. RCH could also be induced by acclimatization at 30 °C for 2 h or anoxia (oxygen-free nitrogen) for 1–2 h. All immature stages showed enhanced survival when acclimatized at 5 °C for 2 h before exposure to ?10 °C. Acclimatization at 30 °C induced RCH only in eggs and deutonymphs, and anoxia was effective for eggs, larvae, and deutonymphs. The variability among immature stages may be attributed to the cost associated with the acclimatization treatments. Our findings suggest that RCH may promote the survival of N. californicus during unexpected changes in temperatures, and can be an important feature particularly when this natural enemy is introduced to non-native environments.