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1.
Glucose-6-phosphate dehydrogenase (G6PD) and glutathione reductase (GR) are metabolically quite important enzymes. Within this study, these two enzymes were purified for the first time from the gills of Lake Van fish. In the purifying process, ammonium sulfate precipitation and 2′,5′-ADP Sepharose 4B affinity column chromatography techniques for glucose-6-phosphate dehydrogenase, temperature degradation and 2′,5′-ADP Sepharose 4B affinity column chromatography for glutathione reductase enzyme were used. The control of the enzyme purity and determination of molecular weight were done with sodium dodecyl sulfate polyacrylamide gel electrophoresis. K M and V max values were determined with Lineweaver–Burk plot. Besides, the effects of some chalcone derivatives on the purified enzymes were analyzed. For the ones showing inhibition effect, % activity–[I] figures were drawn and IC50 values were determined. K i value was calculated by using Cheng–Prusoff equation.  相似文献   

2.
Collagen degradation is known to be involved in the post mortem tenderization of fish muscle. A serine proteinase that is assumed to be related to collagen degradation after fish death was purified from the sarcoplasmic fraction of red sea bream Pagrus major by ammonium sulfate fractionation and column chromatography on Sephacryl S-300, Q Sepharose and Phenyl Sepharose CL-4B. The enzyme hydrolyzed gelatin and was obtained as a protein band of approximately 38 kDa upon sodium dodecyl sulfate polyacrylamide gel electrophoresis under reducing conditions. The N-terminal amino acid sequence of the enzyme was determined for 32 residues. A protein that had the same N-terminal amino acid sequence as the enzyme for ten residues was purified from the serum of red sea bream and showed the same characteristics as the enzyme. Therefore, it is suggested that the serine proteinase migrates from the blood to muscle and degrades muscle proteins after the death of the fish.  相似文献   

3.
Cytosol from brook trout ovarian follicles (stages 1–3) was photoaffinity (PA) labelled using synthetic progestin 17,21-dimethyl-19-nor-pregn-4,9-diene-3,20-dione ([3H]R5020). The covalently bound cytosol protein had a relative mass of 501,000 Mr following Sephacryl S-300 column chromatography. The zona radiata membrane fraction from brook trout oocytes which had gone through the first phase of meiotic maturation (stages 6–7) was isolated by ultracentrifugation of the whole oocytes. The zona radiata solubilized protein presumably from the oocyte membrane was also PA labelled and found to give a peak at 355,000 Mr. The SDS PAGE of the cytosol and zona radiata PA labelled protein gave very similar subunits indicating that the membrane protein and the cytosol protein, both of which bind the maturation inducing steroid (MIS) 17,20-dihydroxy-4-pregnen-3-one (17,20-DHP), have similar subunit structures. The isolated zona radiata protein showed cooperativity of binding to [3H]17,20-DHP and PA labelling to [3H]R5020. The association constant (Ka) was 2.0×107M–1 and maximum binding capacity (Nmax) 427 fmoles/mg protein with MIS [3H]17,20-DHP.No evidence for nuclear binding of MIS [3H]17,20-DHP or PA labelling of [3H]R5020 to nuclei was observed. The nuclei were isolated from stages 1 and 3 fresh ovarian follicles of brook trout. The experimental evidence presented demonstrates the presence of MIS 17,20-DHP receptor-like protein from the zona radiata membranes by PA labelling in brook trout oocytes during final stages of maturation.  相似文献   

4.
The objectives of this study were to isolate and characterize vitellogenin from plasma of estradiol-treated protandrous black porgy,Acanthopagrus schlegeli. Vitellogenin concentrations in plasma measured by a validated enzyme-linked immunosorbent assay (ELISA) were also compared. Two-year-old black porgy (n=20) were fed with estradiol-17 (4 mg kg–1 of feed). Plasma was collected for purification of vitellogenin. Two forms of vitellogenin were found in plasma after chromatography on Sepharose CL-2B column and hydroxylapatite, and polyacrylamide gel electrophoresis. Black porgy vitellogenins are phospho-lipo-glycoproteins based on their chemical staining properties. The apparent molecular weights of the two forms of vitellogenin were 636 kDa and 321 kDa, respectively. The amino acid composition of purified vitellogenin was also analyzed after acid hydrolysis. The presence of immunoreactive vitellogenin was identified in the plasma and mucus extract from control and estradiol-induced females on the basis of Western blotting. Serial dilution of the plasma and mucus extract taken from estradiol-induced black porgy showed reactivity to an antiserum against lipovitellin in the ELISA, whereas mucus extract and plasma from male fish did not. Significantly higher concentrations of plasma vitellogenin were detected in estradiol-stimulated black porgy than in the control males.  相似文献   

5.
硫酸角质素具有丰富的携带大量负电荷的磺酸基团,参与生物矿化的成核过程。磺基转移酶催化磺酸基团的转移,对硫酸角质素的生物合成起决定性作用。本研究利用RACE技术克隆马氏珠母贝磺基转移酶PmCHST1a全长,并通过RNA干扰技术检测PmCHST1a对硫酸角质素合成及贝壳珍珠层形成的影响。结果显示,PmCHST1a基因全长1385 bp,编码366个氨基酸;含有磺基转移酶结构域,具有跨膜结构和信号肽,定位于高尔基体上。组织差异表达分析发现,PmCHST1a在中央膜显著高表达。注射PmCHST1a的RNAi探针后,PmCHST1a在中央膜的表达量显著下调,并且外套膜外液中硫酸角质素的浓度显著降低;SEM检测发现珍珠层结构紊乱。综上所述,PmCHST1a可能通过影响外套膜外液中硫酸角质素的合成,参与珍珠层的形成。本研究为进一步探讨磺基转移酶及其参与合成的糖胺聚糖硫酸角质素在马氏珠母贝生物矿化中的作用提供依据。  相似文献   

6.
We revisit the empirical equation of Gislason et al. (2010, Fish and Fisheries 11 :149–158) for predicting natural mortality (M, year?1) of marine fish. We show it to be equivalent to , where L∞ (cm) and K (year?1) are the von Bertalanffy growth equation (VBGE) parameters, and L (cm) is fish length along the growth trajectory within the species. We then interpret K in terms of the VBGE in mass , and show that the previous equation is itself equivalent to a ?? power function rule between M and the mass at first reproduction (Wα); this new ?? power function emerges directly from the life history that maximizes Darwinian fitness in non‐growing populations. We merge this M, Wα power function with other power functions to produce general across‐species scaling rules for yearly reproductive allocation, reproductive effort and age at first reproduction in fish. We then suggest a new way to classify habitats (or lifestyles) as to the life histories they should contain, and we contrast our scheme with the widely used Winemiller–Rose fish lifestyle classification.  相似文献   

7.
The rate of oxygen consumption of minced whole body was determined volumetrically, as an indication of metabolic rate in vitro (M in vitro ), at 20°C in porgy Pagrus major ranging from 0.0002 g (just after hatch) to 2.9 g (67 days old) in body mass. A triphasic relationship was found between M in vitro of individual fish (l.min–1) and wet body mass W (g). During the prolarval stage accompanied with the transitional period to the postlarval stage (0.00020–0.00023 g, 0–6 days old), the mass-specific metabolic rate in vitro (M in vitro /W in l.g–1.min–1) increased with age (D in days) as expressed by an equation M in vitro /W = 3.88 + 0.74/D. During the postlarval stage (0.00031–0.003 g, 8–22 days old), M in vitro /W remained almost constant, independent of body mass following an equation M in vitro /W = 5.24 W–0.085. During the juvenile and adolescent stages (0.0047–2.9 g, 30–67 days old), M in vitro /W decreased with increasing body mass following an equation M in vitro /W = 1.66 W–0.235. These results correspond with the triphasic relationship between metabolism in vivo and body mass observed in intact porgy of 0.0002–270 g (Oikawa et al. 1991). It is concluded, therefore, that the dependence of mass-specific metabolic rate on body size exists in vitro as well as in vivo, during the early stages in the porgy. Based on these results, factors controlling the metabolism-size relationship are discussed.  相似文献   

8.
Adriatic sturgeon (Acipenser naccarii) were maintained on a commercial diet enriched either in long chain polyunsaturated fatty acids of the 3 series (3 LCPUFA) or in saturated fatty acids (SFA). The effects of dietary fatty acid composition on spontaneous locomotor activity in normoxia and hypoxia (O2 tension = 10.5 ± 0.8 kPa), and on oxygen consumption (MO 2) in normoxia, in hypoxia (O2 tension = 6.6 ± 0.8 kPa) and during recovery were then investigated. The effects of adding supplementary vitamin E to the fat-enriched diets were also studied.Dietary fatty acid composition had effects on spontaneous locomotor activity and MO 2 in normoxia. Activity levels were higher in all sturgeon fed extra dietary fats (without vitamin E), when compared with control animals, but fish fed 3 LCPUFA had a significantly lower MO 2 than those fed SFA, with intermediate MO 2 in controls. In hypoxia, sturgeon 3 LCPUFA did not alter activity or MO 2 whereas those fed SFA reduced both and controls reduced MO 2. During recovery, both animals fed SFA and controls had a higher MO 2 than sturgeon fed 3 LCPUFA. The data indicate that fish fed 3 LCPUFA are more tolerant of hypoxia than controls or those fed SFA, as they did not reduce either activity or MO 2, and consumed less O2 during recovery.Vitamin E supplements modified the effects elicited by dietary fats. All sturgeon fed vitamin E had low activity levels in normoxia and hypoxia. Sturgeon fed vitamin E with 3 LCPUFA had a higher MO 2 in normoxia than those fed 3 LCPUFA alone; reduced MO 2 in hypoxia, and during recovery increased MO 2 to a rate higher than that of animals fed 3 LCPUFA alone. In normoxia, sturgeon fed vitamin E with SFA had a similar MO 2 to those fed SFA alone but did not change MO 2 in hypoxia or during recovery. Thus, the effects of vitamin E were dependent on fat composition of the diet. Vitamin E with 3 LCPUFA removed the beneficial effects on MO 2 and responses to hypoxia obtained with 3 LCPUFA alone, but vitamin E with SFA allowed sturgeon to maintain aerobic metabolism in hypoxia, a more effective response than that observed in fish fed SFA alone.  相似文献   

9.
The C20-22 polyunsaturated fatty acids (C20-22 PUFAs), mainly eicosapentaenoic acid (EPA, 20:5n-3) and docosahexaenoic acid (DHA, 22:6n-3), were concentrated from the refined liver oil of deep sea leafscale gulper shark, Centrophorus squamosus, by sequential processes of winterization, urea complexation, and argentation chromatography. Winterization at 4°C using acetonitrile as solvent showed significant reduction of the total saturated fatty acid content (12%) with a concomitant increase of polyunsaturated fatty acids (36.3%). The urea complexation process significantly enriched the total polyunsaturated fatty acids (49.5%), with a reduction in saturated fatty acids (83.9%). Silica gel based argentation chromatography further concentrated the esters of C20-22 PUFA (>99 percent purity). Nuclear Magnetic Resonance spectroscopy was used as a chemical fingerprinting tool to study the enrichment of C20-22 PUFAs at various stages of the purification process. An increase in the proton signal intensity at the olefinic region (at δ 4–6) and a decrease in the aliphatic signals (at δ 0.5–2) showed that the process successfully enriched the C20-22 PUFAs.

Abbreviations: PUFA, polyunsaturated fatty acid; EPA, eicosapentaenoic acid; DHA, docosahexaenoic acid; FAME, fatty acid methyl esters; SFA, saturated fatty acid; MUFA, monounsaturated fatty acid; NMR, nuclear magnetic resonance; GCMS, gas chromatography mass spectrometry; FFA, free fatty acid.  相似文献   


10.
Trypsin, with molecular weight of 28 kDa from the intestine of genetically improved Nile tilapia (Oreochromis niloticus), was purified by ammonium sulfate precipitation, gel filtration, and anion-exchange chromatography. Purified trypsin had maximal activity at pH 8.0 and 60°C for hydrolysis of N α-p-tosyl-L-arginine methyl ester. The enzyme was stable at temperatures up to 50°C and pH range of 6.0–11.0. Its activity was strongly inhibited by metal ions such as Pb2+ and Fe3+ and protease inhibitors including soybean trypsin inhibitor and phenylmethylsulfonyl fluoride. Also, the ion Ca2+ slightly inhibited this activity. The Michaelis-Menten constant (K m) and catalytic constant (K cat) of purified trypsin were 0.036 mM and 152 s?1, respectively. Furthermore, trypsin contained low amounts of hydrophobic and aromatic amino acids as well as β-sheet (20.2%) and β-turn (25.0%).  相似文献   

11.
  • 1. Annual rate of increase (r) was estimated for the Hooker's sea lion (Phocarctos hookeri) using demographic models that incorporated age-specific estimates of reproductive rate (mx) and survival (lx).
  • 2. In the absence of empirical estimates of natural mortality (nx), survival schedules were derived by combining a range of incidental mortality rates (hx) in commercial fisheries with estimates of nx for two species that exhibit similar life histories to Hooker's sea lions: northern fur seals (Callorhinus ursinus), model A, and Himalayan thar (Hemitragus jemlahicus), model B. Model A represented a population that would have a limited capacity for population increase; incidental mortality rates of mature females above about lo would result in a population decline. Model B represented a population that, even in the absence of incidental mortalities, would just remain stable.
  • 3. If either of these models accurately represents the population demography of Hooker's sea lions, then these animals have limited capacity for population increase. They are constrained by relatively delayed maturity, moderate reproductive rates and short life spans.
  • 4. While absolute estimates of r from our models must be interpreted with caution, it is the responses of r to incidental mortalities and to increased natural mortality of pups that are most informative. Both models show r decreasing by 0.007–0.008 with a 0.01 increase in incidental mortalities of mature females. Both models also indicate that an increase in the natural mortality of pups by 0.027 will reduce r by 0.0055 or more.
  • 5. Given the paucity of available empirical data, our results suggest that incidental mortalities of Hooker's sea lions in the trawl fishery for arrow squid (Nototodarus sloanii) should be minimized if a population decline is to be avoided.
  相似文献   

12.
Energy budget calculations, based on published values for changes in biochemical composition and oxygen consumption, have confirmed that metamorphosing bonefish (Albula sp.) larvae from the Gulf of California receive all of their metabolic energy requirements from the breakdown of endogenous reserves. The calculations showed that during metamorphosis, about 80% of the energy was supplied by lipid, and most of the remainder was provided by keratan sulfate glycosaminoglycan. These results support the suggestion that keratan sulfate can function as a storage polysaccharide, a novel function for glycosaminoglycans in vertebrates.  相似文献   

13.
The wake generated by a screen or a net is analysed by the linear free-wake equations in conjunction with an eddy viscosity formulation. The behaviour of the near and far-field wake is investigated, and a relationship between the drag coefficient and the wake velocity is derived. A method for calculating the current forces experienced by the net structure and the resulting deformation is derived and compared with model tests. The effects of the wake behaviour and the deformation of the net cages, on the design and operation of floating fish farms are discussed and some recommendations are given.Nomenclature A Area of a net panel - dA Area of a portion of a net panel - A N Area of the net panel normal to the flow direction - A P Area of the net panel parallel to the flow direction - CD,i Drag coefficient of thei th cylinder - CD() Drag coefficient as function of the angle between the normal to the net and flow direction - CL() Lift coefficient as function of the angle between the normal to the net and flow direction - D Diameter - D i Diameter of thei th cylinder - DO Dissolved oxygen concentration - F D Drag force - F L Lift force - H Heaviside function - L Width of net panel - l i Length of thei th cylinder - N Number of cylinders - N i Number of cylinders in y-direction - N j Number of cylinders in z-direction - N N Number of cages in direction normal to the flow - N C Number of cages in direction of the flow - r=u/U Velocity reduction factor - Rn=U*D/v Reynolds number - Sn Solidity ratio, defined as the ratio between the area covered by the threads and the total area of the net panel - t Time - U Current or free flow velocity - u 1=U–u Velocity defect - u=U–u 1 Wake velocity - x,y,z Cartesian coordinate system or field point for calculation of velocity - x i ,y i ,z i Source point on screen element - Angle between the flow direction and the normal vector to the net, in the direction of the flow - Eddy viscosity - Mesh size - Kinematic viscosity - Density of water - Error function - Partial differential operator - Infinity  相似文献   

14.
In this study, the molecular mobility of fish flesh was measured by low field nuclear magnetic resonance (LF-NMR) relaxation. Sardine, tuna and mackerel were frozen at ?40 °C and stored for 1 day (24 h); and then these samples were thawed at room temperature (20 °C). The relaxation of water protons in fish flesh was measured for fresh (i.e., before freezing) and multi-cycle freeze–thaw samples (i.e., up to 12 times). Three domains from different pools of protons (i.e., low-mobile, medium-mobile and high-mobile) were identified from the relaxation curve. The T 2b (low-mobile), T 21 (medium-mobile) and T 22 (high-mobile) indicated the proton populations in the protein molecules, strongly bound water molecules, and weakly bound water molecules, respectively. In all cases, the relaxation time (T 2b: sardine r = 0.736 and p < 0.01, tuna r = 0.857 and p < 0.001, mackerel r = 0.904 and p < 0.001; and T 22: sardine r = 0.956 and p < 0.0001, tuna r = 0.927 and p < 0.0001, mackerel r = 0.890 and p < 0.0001) increased with the freeze–thaw cycles and it reached a nearly constant value after 6 freeze–thaw cycles. The increased relaxation time (i.e., higher mobility) up to 6 freeze–thaw cycles could be due to the increase in proton mobility. However, relaxation time (T 21: sardine r = ?0.510 and p > 0.05, tuna r = 0.162 and p > 0.5, mackerel r = 0.513 and p > 0.01) showed insignificant change with the increase of freeze–thaw cycles, which indicated minimal change in the medium-mobile protons. The results in this study revealed that the changes in proton mobility in the fish flesh during freeze–thaw cycles could be identified using T 2b and T 22 relaxation of LF-NMR.  相似文献   

15.
Three pepsinogens (PG1, PG2, and PG3) were highly purified from the stomach of freshwater fish rice field eel (Monopterus albus Zuiew) by ammonium sulfate fractionation and chromatographies on DEAE-Sephacel, Sephacryl S-200 HR. The molecular masses of the three purified PGs were all estimated as 36 kDa using SDS–PAGE. Two-dimensional gel electrophoresis (2D-PAGE) showed that pI values of the three PGs were 5.1, 4.8, and 4.6, respectively. All the PGs converted into corresponding pepsins quickly at pH 2.0, and their activities could be specifically inhibited by aspartic proteinase inhibitor pepstatin A. Optimum pH and temperature of the enzymes for hydrolyzing hemoglobin were 3.0–3.5 and 40–45°C. The K m values of them were 1.2 × 10−4 M, 8.7 × 10−5 M, and 6.9 × 10−5 M, respectively. The turnover numbers (k cat) of them were 23.2, 24.0, and 42.6 s−1. Purified pepsins were effective in the degradation of fish muscular proteins, suggesting their digestive functions physiologically.  相似文献   

16.
During metamorphosis of leptocephalous larvae of the bonefish (Albula sp.), keratan sulfate, the principal glycosaminoglycan of the extracellular gelatinous body matrix, is degraded. Artificial substrates have been utilized to demonstrate the presence of β-N-acetylglucosaminidase, β-galactosidase and sulfatase activities in whole-body homogenates of early metamorphosing leptocephali. The concerted action of these enzymes has been shown to degrade the keratan sulfate polymer in other tissues. This paper describes the extraction, partial purification and some of the physical and kinetic properties of these enzymes. Additionally, starch gel electrophoresis was used to follow glycosidase activities in early, intermediate and advanced metamorphosing larvae. No differences were observed in electrophoretic migration or banding pattern of either β-N-acetylglucosaminidase or β-galactosidase during metamorphosis.  相似文献   

17.
Two forms of rhodanese were purified from the liver of Clarias gariepinus Burchell, designated catfish rhodanese I (cRHD I) and rhodanese II (cRHD II), by ion-exchange chromatography on a CM-Sepharose CL-6B column and gel filtration through a Sephadex G-75 column. The apparent molecular weight obtained for cRHD I and cRHD II was 34,500 ± 707 and 36,800 ± 283 Da, respectively. The subunit molecular weight determined by sodium dodecyl sulphate–polyacrylamide gel electrophoresis was 33,200 ± 283 and 35,100 ± 141 Da for cRHD I and cRHD II, respectively. Atomic absorption spectrophotometric analysis revealed that cRHD II contained a high level of iron (Fe), which presumably was responsible for the brownish colour of the preparation. In contrast, no Fe was identified in cRHD I, and its preparation was colourless. Further characterization of cRHD II gave true Michaelis–Menten constant (K m) values of 25.40 ± 1.70 and 18.60 ± 1.68 mM for KCN and Na2S2O3, respectively, an optimum pH of 6.5 and an optimum temperature of 40°C. The Arrhenius plot of the effects of temperature on the reaction rate consisted of two linear segments with a break occurring at 40°C. The apparent activation energy values from these slopes were 7.3 and 72.9 kcal/mol. Inhibition studies on the cRHD II enzyme showed that the activity of the enzyme was not affected by Mn2+, Co2+, Sn2+, Ni2+ and NH4 +, but Zn2+ inhibited the enzyme considerably.  相似文献   

18.
The incorporation, and the capacity for desaturation and elongation in vivo, of intraperitoneally-injected, 14C-labelled n–3 and n–6 C18 and C20 PUFAs were investigated in juvenile gilthead sea bream, Sparus aurata. The results indicate that juvenile gilthead sea bream have only limited ability to convert CH PUFAs to C20 and C22 HUFAs in vivo. The data are consistent with the results from nutritional studies on larvae, postlarvae and fingerlings that have shown that gilthead sea bream require the provision of preformed eicosapentaenoic and docosahexaenoic acids in the diet. The impairment in the desaturase/elongase pathway was quantitatively and qualitatively similar to that found in turbot, Scophthalmus maximus, being at the level of the 5-desaturase. The low activity of 5-desaturase combined with the consistent finding that arachidonic acid is selectively retained in membrane phosphatidylinositol suggests that, in addition to eicosapentaenoic and docosahexaenoic acids, gilthead sea bream may also have a requirement for preformed arachidonic acid in the diet.Abbreviations AA 5,8,11,14-eicosapenaenoic acid (arachidonic acid, 20:4n–6) - CPL diradyl (diacyl + alkenylacyl + alkylacyl) glycerophosphocholine - DHA 4,7,10,13,16,19-docosahexaenoic acid (22:6n–3) - EPA 5,8,11,14,17-eicosapentaenoic acid (20:5n–3) - EPL diradyl (diacyl, alkenylacyl + alkylacyl) glycerophosphoethanolamine - HUFA highly unsaturated fatty acids ( C20 and with 3 double bonds) - LA 9,12-octadecadienoic acid (linoleic acid, 18:2n–6) - LNA 9,12,15-octadecatrienoic acid (-linolenic acid, 18:3n–3) - PI phosphatidylinositol - PS phosphatidylserine - PUFA polyunsaturated fatty acid(s)  相似文献   

19.
The glutathione S-transferases of fish   总被引：1，自引：0，他引：1  
Substantial soluble glutathione S-transferase activity and millimolar reduced glutathione (GSH) are present in most tissues of both teleosts and elasmobranchs. The hepatic enzymes of fish conjugate a range of electrophilic substrates with GSH, although their specificities are less broad than those of the transferases in rodent liver. There is no good evidence that fish transferases have ligandin-like activity or a suicide function. All fish livers tested have several transferase isoenzymes. They are dimers of subunits whose Mrs are about 25 kDa and which may have different catalytic properties. In some species transferase activity is induced by agents such as phenols or 3-methylcholanthrene. Glutathione S-transferases are important detoxication enzymes in fish.  相似文献   

20.
A novel marine origin Bacillus subtilis strain H1 isolated from a shrimp culture pond effectively removed NH4+‐N, ‐N and ‐N, with a maximum ammonium, nitrite and nitrate removal rate of 2.35 mg NH4+‐N L?1 hr?1 per OD, 9.64 mg ‐N L?1 hr?1 per OD and 0.75 mg ‐N L?1 hr?1 respectively. The gas chromatography–isotope ratio mass spectrometry results indicated that N2O was emitted when 15NH4Cl, Na15NO2 or Na15NO3 was used. Additionally, N2 was also produced when Na15NO2 was used. Single‐factor experiments suggested that the optimal conditions for NH4+‐N and ‐N removal were glucose as a carbon source, C/N 15, initial pH 7.5, 30 g/L NaCl, 28°C and a shaking speed of 160 rpm. Orthogonal tests showed that the optimal conditions for NH4+‐N removal were C/N 15, pH 9, 10 g/L NaCl and shaking speed 160 rpm when ammonium chloride was used as the substrate. The optimal conditions for ‐N removal were C/N 10, pH 6, 10 g/L NaCl and a shaking speed of 160 rpm when sodium nitrite was used as the substrate. In summary, B. subtilis strain H1 had highly efficient aerobic nitrifying–denitrifying ability and high adaptability, suggesting that it is potentially valuable to marine aquaculture.  相似文献   

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