RESUMEN
We explored picophytoplankton in the surface (0 m) and bottom (2.3-8.7 m) layers of a shallow (<10 m) eutrophic coastal system (Isahaya Bay, Japan). We found that picophytoplankton (principally Synechococcus) constituted the major phytoplankton in spring and summer. The chlorophyll a (chl.a) concentration in the 0.7-2.0-µm picophytoplankton fraction (hereinafter 'pico-sized chl. a') and picophytoplankton abundance in Isahaya Bay were higher than those in other eutrophic coastal waters. The pico-sized chl. a concentration and the picophytoplankton abundance counted with an epifluorescence microscope was up to 49.31 µg L-1 and 1.9 × 106 cells mL-1, respectively. Higher contributions of pico-sized chl. a to the total chl. a were evident in summer (up to 63.5%), relative to spring (up to 32.1%), at both depths. Picophytoplankton abundance and the pico-sized chl. a concentration was positively correlated with water temperature and dissolved inorganic phosphorus (DIP) concentrations. Thus, both temperature and DIP may be major controllers of picophytoplankton in Isahaya Bay. The pico-sized chl. a concentration and picophytoplankton cell number at the bottom layer were positively correlated with those in the surface layer, suggesting that picophytoplankton in bottom layers may have sunk from the surface layers. The results imply that the picophytoplankton affects the biogeochemical processes in the bottom of Isahaya Bay more than previously thought. This may be true not only for this estuary but also for other eutrophic coastal seas.
Asunto(s)
Fitoplancton , Agua , Biomasa , Clorofila A , Estaciones del Año , Clorofila/metabolismoRESUMEN
BACKGROUND/AIM: Human lung adenocarcinoma PC14 cells without mutations in the epidermal growth factor receptor (EGFR) are less sensitive to gefitinib than PC9 cells with EGFR mutations. We report the involvement of tetrandrine in autophagy flux as a mechanism that enhances the sensitivity of PC14 cells to gefitinib. MATERIALS AND METHODS: Sensitivity to gefitinib was determined by a growth inhibition assay, and quantitative real-time PCR, western blotting, and fluorescent immunostaining were used to detect autophagy. RESULTS: In PC14 cells, combined treatment with gefitinib and tetrandrine caused a significant increase in gefitinib sensitivity and autophagy-related mRNAs and proteins (LC3, etc.), and the LC3 protein accumulated in lysosomes. Furthermore, an autophagy flux assay revealed that tetrandrine inhibited lysosomes and that gefitinib promoted autophagy. Finally, the sensitivity of PC14 cells to gefitinib was enhanced with chloroquine. CONCLUSION: Tetrandrine possibly increases the susceptibility of PC14 cells to gefitinib by lysosomal inhibition.
Asunto(s)
Adenocarcinoma del Pulmón/metabolismo , Bencilisoquinolinas/farmacología , Gefitinib/farmacología , Neoplasias Pulmonares/metabolismo , Lisosomas/metabolismo , Proteínas Asociadas a Microtúbulos/metabolismo , Adenocarcinoma del Pulmón/tratamiento farmacológico , Adenocarcinoma del Pulmón/genética , Autofagia , Bencilisoquinolinas/química , Línea Celular Tumoral , Proliferación Celular/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Resistencia a Antineoplásicos/efectos de los fármacos , Sinergismo Farmacológico , Receptores ErbB/genética , Gefitinib/química , Regulación Neoplásica de la Expresión Génica/efectos de los fármacos , Humanos , Neoplasias Pulmonares/tratamiento farmacológico , Neoplasias Pulmonares/genética , Lisosomas/efectos de los fármacos , Proteínas Asociadas a Microtúbulos/genéticaRESUMEN
Fish are reported to exhibit chitinase activity in the stomach. Analyses of fish stomach chitinases have shown that these enzymes have the physiological function of degrading chitinous substances ingested as diets. Osteichthyes, a group that includes most of the fishes, have several chitinases in their stomachs. From a phylogenetic analysis of the chitinases of vertebrates, these particular molecules were classified into a fish-specific group and have different substrate specificities, suggesting that they can degrade ingested chitinous substances efficiently. On the other hand, it has been suggested that coelacanth (Sarcopterygii) and shark (Chondrichthyes) have a single chitinase enzyme in their stomachs, which shows multiple functions. This review focuses on recent research on the biochemistry of fish stomach chitinases.
Asunto(s)
Quitinasas/química , Quitinasas/metabolismo , Peces , Estómago/enzimología , Animales , Quitinasas/genética , Humanos , Transporte de ProteínasRESUMEN
Fish express two different chitinases, acidic fish chitinase-1 (AFCase-1) and acidic fish chitinase-2 (AFCase-2), in the stomach. AFCase-1 and AFCase-2 have different degradation patterns, as fish efficiently degrade chitin ingested as food. For a comparison with the enzymatic properties and the primary structures of chitinase isozymes obtained previously from the stomach of demersal fish, in this study, we purified chitinase isozymes from the stomach of Japanese sardine Sardinops melanostictus, a surface fish that feeds on plankton, characterized the properties of these isozymes, and cloned the cDNAs encoding chitinases. We also predicted 3D structure models using the primary structures of S. melanostictus stomach chitinases. Two chitinase isozymes, SmeChiA (45 kDa) and SmeChiB (56 kDa), were purified from the stomach of S. melanostictus. Moreover, two cDNAs, SmeChi-1 encoding SmeChiA, and SmeChi-2 encoding SmeChiB were cloned. The linker regions of the deduced amino acid sequences of SmeChi-1 and SmeChi-2 (SmeChi-1 and SmeChi-2) are the longest among the fish stomach chitinases. In the cleavage pattern groups toward short substrates and the phylogenetic tree analysis, SmeChi-1 and SmeChi-2 were classified into AFCase-1 and AFCase-2, respectively. SmeChi-1 and SmeChi-2 had catalytic domains that consisted of a TIM-barrel (ß/α)8-fold structure and a deep substrate-binding cleft. This is the first study showing the 3D structure models of fish stomach chitinases.
Asunto(s)
Quitinasas/metabolismo , Peces , Mucosa Gástrica/metabolismo , Isoenzimas/metabolismo , Animales , Quitinasas/química , Quitinasas/genética , Clonación Molecular , Isoenzimas/química , Isoenzimas/genética , Japón , Filogenia , Agua de MarRESUMEN
A 56 kDa chitinase isozyme (PaChiB) was purified from the stomach of the silver croaker Pennahia argentatus. The optimum pH and pH stability of PaChiB were observed in an acidic pH range. When N-acetylchitooligosaccharides ((GlcNAc)n, n=2 -6) were used as substrates, PaChiB degraded (GlcNAc)4 -6 and produced (GlcNAc)2,3. It degraded (GlcNAc)5 to produce (GlcNAc)2 (23.2%) and (GlcNAc)3 (76.8%). The ability to degrade p-nitrophenyl N-acetylchitooligosaccharides (pNp-(GlcNAc)n, n=2 -4) fell in the following order: pNp-(GlcNAc)3â« pNp-(GlcNAc)2 pNp-(GlcNAc)4. Based on these results, we concluded that PaChiB is an endo-type chitinolytic enzyme, and that it preferentially hydrolyzes the third glycosidic bond from the non-reducing end of (GlcNAc)n. Activity toward crystalline α- and ß-chitin was activated at 124%-185% in the presence of 0.5 M NaCl. PaChiB exhibited markedly high substrate specificity toward crab-shell α-chitin.
Asunto(s)
Quitina/metabolismo , Quitinasas/aislamiento & purificación , Perciformes/metabolismo , Estómago/química , Secuencia de Aminoácidos , Animales , Quitinasas/química , Cromatografía Líquida de Alta Presión , Concentración de Iones de Hidrógeno , Hidrólisis , Isoenzimas/química , Isoenzimas/aislamiento & purificación , Cinética , Datos de Secuencia Molecular , Peso Molecular , Nitrofenoles/química , Oligosacáridos/metabolismo , Alineación de Secuencia , Cloruro de Sodio/química , Estómago/enzimología , Especificidad por Sustrato , TemperaturaRESUMEN
A chitinase was purified from the stomach of a fish, the silver croaker Pennahia argentatus, by ammonium sulfate fractionation and column chromatography using Chitopearl Basic BL-03, CM-Toyopearl 650S, and Butyl-Toyopearl 650S. The molecular mass and isoelectric point were estimated at 42 kDa and 6.7, respectively. The N-terminal amino acid sequence showed a high level of homology with family 18 chitinases. The optimum pH of silver croaker chitinase toward p-nitrophenyl N-acetylchitobioside (pNp-(GlcNAc)2) and colloidal chitin were observed to be pH 2.5 and 4.0, respectively, while chitinase activity increased about 1.5- to 3-fold with the presence of NaCl. N-Acetylchitooligosaccharide ((GlcNAc)n, n = 2-6) hydrolysis products and their anomer formation ratios were analyzed by HPLC using a TSK-GEL Amide-80 column. Since the silver croaker chitinase hydrolyzed (GlcNAc)4-6 and produced (GlcNAc)2-4, it was judged to be an endo-type chitinase. Meanwhile, an increase in beta-anomers was recognized in the hydrolysis products, the same as with family 18 chitinases. This enzyme hydrolyzed (GlcNAc)5 to produce (GlcNAc)2 (79.2%) and (GlcNAc)3 (20.8%). Chitinase activity towards various substrates in the order pNp-(GlcNAc)n (n = 2-4) was pNp-(GlcNAc)2 >> pNp-(GlcNAc)4 > pNp-(GlcNAc)3. From these results, silver croaker chitinase was judged to be an enzyme that preferentially hydrolyzes the 2nd glycosidic link from the non-reducing end of (GlcNAc)n. The chitinase also showed wide substrate specificity for degrading alpha-chitin of shrimp and crab shell and beta-chitin of squid pen. This coincides well with the feeding habit of the silver croaker, which feeds mainly on these animals.