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1.
Prikl Biokhim Mikrobiol ; 45(1): 78-83, 2009.
Article in English | MEDLINE | ID: mdl-19235513

ABSTRACT

The distillery wastewater (spent wash) contains dark-brown colored recalcitrant organic compounds that are not amenable to conventional biological treatment. The characteristic recalcitrance to decolorization is due to the presence of brown melanoidin polymers. In the present study, feasibility of using Pseudomonas putida strain U for decolorization of spent wash was demonstrated. Batch cultures of P. putida decolourized spent wash by 24%, 2- fold higher decolorization was achieved following immobilization in calcium alginate beads. Glucose concentration was critical for decolourization and improved color removal efficiency was obtained by periodic replenishment of glucose. Decolourization was also observed with lactose or whey as alternative carbon sources. The results of our study suggest that P. putida could be used for biological decolorization of molasses spent washes and that supplementation with whey (a by-product from cheese industry) can offer economical viability to the process.


Subject(s)
Color , Molasses , Pseudomonas putida/metabolism , Waste Disposal, Fluid , Biodegradation, Environmental , Bioreactors , Glucose/metabolism , Lactose/metabolism , Polymers/chemistry , Water Purification/methods
2.
Exp Oncol ; 27(4): 279-85, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16404347

ABSTRACT

AIM: To develop a rationally designed new nitrogen mustard namely Fluorenhymustine (compound 2), where N,N'-bis(2chloro-ethyl)amino group, the established anticancer functionality, is attached to the 2-ethyl fluorenone hydantoin moiety. MATERIALS AND METHODS: Starting from fluorenone hydantoin, a 3-step synthetic procedure was followed to obtain the title compound. 4-(4-Nitrobenzyl)pyridine was used to assess its chemical alkylating activity. Murine tumors (Ehrlich ascites carcinoma (EAC) and Sarcoma-180 (S-180)) were used to assess its in vivo activity. Its cytotoxicity was determined in vitro in MCF-7 human breast tumor cell line, toxicity - in vivo in normal and EAC bearing mice. 3H-Thymidine and 3H-Uridine were employed to study its inhibitory effect on DNA and RNA synthesis respectively in S-180 tumor cells in vitro. RESULTS: Alkylating activity of fluorenmustine exceeded that of N-di(2-chloroethyl)amine used as a standard alkylating compound. It has displayed an excellent and reproducible antitumor activity in vivo against EAC and S-180 comparable to that of 5-fluorouracil judging by the increase in median survival times of treated animals. It also significantly increased the life span of mice bearing advanced tumors for 6 days before the drug challenge. However in vitro screening in MCF-7 did not reveal any significant cytotoxicity. The compound did not adversely affect hematopoiesis at its optimum dose. Drug-induced hepatotoxicity and nephrotoxicity were also not detected. It inhibited the synthesis of DNA and RNA in S-180 tumor cells at 8 microM concentration. CONCLUSION: Results indicated promising chemotherapeutic potential of Fluorenhymustine.


Subject(s)
Antineoplastic Agents, Alkylating/pharmacology , Neoplasms, Experimental/drug therapy , Nitrogen Mustard Compounds/pharmacology , Animals , Antineoplastic Agents, Alkylating/chemical synthesis , Cell Line, Tumor , Dose-Response Relationship, Drug , Drug Evaluation, Preclinical , Drug Screening Assays, Antitumor , Humans , Mice , Nitrogen Mustard Compounds/chemical synthesis
3.
Neuroscience ; 125(2): 449-59, 2004.
Article in English | MEDLINE | ID: mdl-15062987

ABSTRACT

A neurogenic component has been suggested to play a pivotal role in a range of inflammatory/immune diseases. Mustard oil (allyl-isothiocyanate) has been used in studies of inflammation to mediate neurogenic vasodilatation and oedema in rodent skin. The aim of the present study was to analyse mustard oil-induced oedema and neutrophil accumulation in the mouse ear focussing on the roles of neurokinin 1 (NK(1)) and vanilloid (TRPV1) receptors using normal (BALB/c, C57BL/6) as well as NK(1) and TRPV1 receptor knockout mice. A single or double treatment of 1% mustard oil on the BALB/c mouse ear induced ear oedema with responses diminished by 6 h. However a 25-30% increase in ear thickness was maintained by the hourly reapplication of mustard oil. Desensitisation of sensory nerves with capsaicin, or the NK(1) receptor antagonist SR140333, inhibited oedema but only in the first 3 h. Neutrophil accumulation in response to mustard oil was inhibited neither by SR140333 nor capsaicin pre-treatment. An activating dose of capsaicin (2.5%) induced a large oedema in C57BL/6 wild-type mice that was minimal in TRPV1 receptor knockout mice. By comparison, mustard oil generated ear swelling was inhibited by SR140333 in wild-type and TRPV1 knockout mice. Repeated administration of mustard oil maintained 35% oedema in TRPV1 knockout animals and the lack of TRPV1 receptors did not alter the leukocyte accumulation. In contrast repeated treatment caused about 20% ear oedema in Sv129+C57BL/6 wild-type mice but the absence of NK(1) receptors significantly decreased the response. Neutrophil accumulation showed similar values in both groups. This study has revealed that mustard oil can act via both neurogenic and non-neurogenic mechanisms to mediate inflammation in the mouse ear. Importantly, the activation of the sensory nerves was still observed in TRPV1 knockout mice indicating that the neurogenic inflammatory component occurs via a TRPV1 receptor independent process.


Subject(s)
Inflammation/classification , Plant Extracts/toxicity , Receptors, Drug/metabolism , Receptors, Neurokinin-1/metabolism , Animals , Capillary Permeability/drug effects , Capsaicin/pharmacology , Dose-Response Relationship, Drug , Ear/innervation , Edema/chemically induced , Inflammation/chemically induced , Mice , Mice, Inbred BALB C , Mice, Inbred C57BL , Mice, Knockout , Mustard Plant , Neurokinin-1 Receptor Antagonists , Piperidines/pharmacology , Plant Oils , Quinuclidines/pharmacology , Receptors, Drug/genetics , Receptors, Neurokinin-1/genetics , Staining and Labeling/methods , TRPV Cation Channels , Time Factors
4.
Lett Appl Microbiol ; 34(6): 398-401, 2002.
Article in English | MEDLINE | ID: mdl-12028418

ABSTRACT

AIMS: The present study describes the detection and quantification of the Sarocladium oryzae metabolites, helvolic acid and cerulenin in extracts of rice grains collected from plants infected with sheath rot. It also describes the phytotoxicity of these metabolites on rice seedlings. METHODS AND RESULTS: Helvolic acid and cerulenin in sheath rot-infected rice grains were detected using thin layer chromatography (TLC) and nuclear magnetic resonance (NMR) analyses. On the TLC plates helvolic acid and cerulenin moved as brownish yellow spots and showed R(F) values of 0.61 and 0.49, respectively. A standard assay curve was developed on the basis of selective toxicity of helvolic acid towards Calvibacter michiganensis ATCC 2140 and cerulenin towards Candida albicans 1150. The amounts of helvolic acid and cerulenin on the basis of standard assay curve were 2.2 and 1.75 microg g(-1) of infected seeds. Treatment of IR 36 rice seedlings with metabolites induced chlorosis and reduced shoot length by 20%, root length by 30% and root number by 7% relative to control. CONCLUSIONS: Helvolic acid and cerulenin were detected in infected rice grains and these metabolites induced chlorosis and reduced the seed viability and seedling health of rice. SIGNIFICANCE AND IMPACT OF THE STUDY: Antimicrobial and phytotoxic metabolites, helvolic acid and cerulenin are present in infected grains and reduce the seed viability and seedling health. These metabolites may increase the pathogenic potential and survival of S. oryzae in rice seed by competing with other seed-borne fungi.


Subject(s)
Cerulenin/analysis , Edible Grain/microbiology , Fusidic Acid/analogs & derivatives , Fusidic Acid/analysis , Oryza/microbiology , Chromatography, Thin Layer , Edible Grain/chemistry , Magnetic Resonance Spectroscopy , Oryza/chemistry , Plant Diseases/microbiology , Plant Extracts , Sesquiterpenes , Terpenes , Phytoalexins
5.
Biochem J ; 339 ( Pt 3): 667-73, 1999 May 01.
Article in English | MEDLINE | ID: mdl-10215606

ABSTRACT

The unique catalytic characteristics of adenosine kinase (Adk) and its stage-specific differential activity pattern have made this enzyme a prospective target for chemotherapeutic manipulation in the purine-auxotrophic parasitic protozoan Leishmania donovani. However, nothing is known about the structure of the parasite Adk. We report here the cloning of its gene and the characterization of the gene product. The encoded protein, consisting of 345 amino acid residues with a calculated molecular mass of 37173 Da, shares limited but significant similarity with sugar kinases and inosine-guanosine kinase of microbial origin, supporting the notion that these enzymes might have the same ancestral origin. The identity of the parasite enzyme with the corresponding enzyme from two other sources so far described was only 40%. Furthermore, 5' RNA mapping studies indicated that the Adk gene transcript is matured post-transcriptionally with the trans-splicing of the mini-exon (spliced leader) occurring at nt -160 from the predicted translation initiation site. The biochemical properties of the recombinant enzyme were similar to those of the enzyme isolated from leishmanial cells. The intrinsic tryptophan fluorescence of the enzyme was substrate-sensitive. On the basis of a multiple protein-alignment sequence comparison and ATP-induced fluorescence quenching in the presence or the absence of KI and acrylamide, the docking site for ATP has been provisionally identified and shown to have marked divergence from the consensus P-loop motif reported for ATP- or GTP-binding proteins from other sources.


Subject(s)
Adenosine Kinase/chemistry , Adenosine Kinase/metabolism , Adenosine Triphosphate/metabolism , Leishmania donovani/enzymology , Acrylamide/metabolism , Adenosine Kinase/genetics , Adenosine Kinase/isolation & purification , Amino Acid Sequence , Animals , Base Sequence , Binding Sites , Cloning, Molecular , Consensus Sequence/genetics , Escherichia coli/genetics , Fluorescence , Humans , Kinetics , Leishmania donovani/genetics , Molecular Sequence Data , Molecular Weight , Open Reading Frames/genetics , Potassium Iodide/metabolism , RNA, Messenger/analysis , RNA, Messenger/genetics , Recombinant Proteins/biosynthesis , Recombinant Proteins/chemistry , Recombinant Proteins/isolation & purification , Recombinant Proteins/metabolism , Sequence Homology, Amino Acid , Trans-Splicing/genetics , Tryptophan/metabolism
6.
Antimicrob Agents Chemother ; 40(11): 2610-7, 1996 Nov.
Article in English | MEDLINE | ID: mdl-8913474

ABSTRACT

Siderophores selectively bind ferric iron and are involved in receptor-specific iron transport into bacteria. Several types of siderophores were synthesized, and growth-promoting or inhibitory activities when they were conjugated to carbacephalosporin, erythromycylamine, or nalidixic acid were investigated. Overall, 11 types of siderophores and 21 drug conjugates were tested against seven different bacterial species: Escherichia coli, Bordetella bronchiseptica, Pasteurella multocida, Pasteurella haemolytica, Streptococcus suis, Staphylococcus aureus, and Staphylococcus epidermidis. In some species, the inhibitory activities of the drug conjugates were associated with the ability of the bacteria to use the siderophore portion of the molecules for growth promotion in disc diffusion tests (0.04 mumol of conjugate or siderophore per disc). E. coli used catechol-based siderophore portions as well as hydroxamate-based tri-delta-OH-N-OH-delta-N-acetyl-L-ornithine ferric iron ligands for growth under iron-restricted conditions achieved by supplemental ethylenediamine di (O-hydroxyphenylacetic acid) (100 micrograms/ml) and was sensitive to carbacephalosporin conjugated to these siderophore types (up to a 34-mm-diameter inhibition zone). B. bronchiseptica used desferrioxamine B and an isocyanurate-based or trihydroxamate in addition to catechol-based siderophore portions for promotion but was not inhibited by beta-lactam conjugates partly because of the presence of beta-lactamase. P. multocida and P. haemolytica did not use any of the synthetic siderophores for growth promotion, and the inhibitory activities of some conjugates seemed partly linked to their ability to withhold iron from these bacteria, since individual siderophore portions showed some antibacterial effects. Individual siderophores did not promote S. suis growth in restrictive conditions, but the type of ferric iron ligands attached to beta-lactams affected inhibitory activities. The antibacterial activities of the intracellular-acting agents erythromycylamine and nalidixic acid were reduced or lost, even against S. aureus and S. epidermidis, when the agents were conjugated to siderophores. Conjugate-resistant E. coli mutants showed the absence of some iron-regulated outer membrane proteins in gel electrophoresis profiles and in specific phage or colicin sensitivity tests, implying that the drugs used outer membrane receptors of ferric complexes to get into cells.


Subject(s)
Anti-Bacterial Agents/metabolism , Bacteria/metabolism , Iron/metabolism , Siderophores/metabolism , Swine Diseases/microbiology , Animals , Anti-Bacterial Agents/chemistry , Bacteria/genetics , Bacterial Outer Membrane Proteins/metabolism , Bordetella/genetics , Bordetella/growth & development , Bordetella/metabolism , Colicins/pharmacology , Drug Resistance, Microbial , Escherichia coli/drug effects , Escherichia coli/genetics , Hydroxamic Acids/pharmacology , Microbial Sensitivity Tests , Mutation , Pasteurella/genetics , Pasteurella/growth & development , Pasteurella/metabolism , Siderophores/chemistry , Streptococcus suis/genetics , Streptococcus suis/growth & development , Streptococcus suis/metabolism , Swine
7.
Indian J Pediatr ; 63(2): 189-98, 1996.
Article in English | MEDLINE | ID: mdl-10829988

ABSTRACT

Cystic fibrosis (CF) is a common inherited disorder in caucasians. The estimated incidence of CF in Asians varies from 1:10,000 to 1:12,000. Indian data is restricted to few case reports. The gene for CF is located on the long arm of chromosome 7 at position 7q13. There are more than 300 identified mutations in CF. The basic defect in CF is a mutational change in the gene for chloride conductance channel. Failure of chloride conductance by epithelial cells leads to dehydration of secretions that are too viscid and difficult to clear. The disease is characterized by abnormal secretions in the respiratory, gastrointestinal and reproductive tract and sweat glands. The common clinical manifestations include meconium ileus in neonatal period, recurrent lower respiratory tract infections (pseudomonas pneumonia, bronchiectasis), steatorrhoea, azoospermia, and in late stages hepatobiliary and endocrine pancreatic dysfunctions. The diagnosis of disease is established by clinical criteria and sweat chloride concentration more than 60 mEq/L. Facilities for DNA diagnosis of common CF mutations are now available in India. The treatment of CF includes early diagnosis, daily clearance of respiratory passages, appropriate antibiotic therapy, aerosolised recombinant human DNase and antibiotics, and nutritional supplementation. The latter include changes in diet composition, pancreatic enzyme supplementation and vitamins and trace mineral supplementation. Gene therapy for the pulmonary manifestations is being tried in a number of centres abroad. Other considerations include heart lung transplantation and ameloride inhalation therapy.


Subject(s)
Anti-Bacterial Agents/administration & dosage , Cystic Fibrosis/diagnosis , Cystic Fibrosis/therapy , Prenatal Diagnosis , Respiratory Therapy/methods , Adolescent , Child , Child Nutritional Physiological Phenomena , Child, Preschool , Combined Modality Therapy , Cystic Fibrosis/physiopathology , Female , Humans , India , Male , Pregnancy , Prognosis
8.
Cancer Lett ; 85(1): 65-72, 1994 Sep 30.
Article in English | MEDLINE | ID: mdl-7923104

ABSTRACT

The toxicity of cypenhymustine, a potential anticancer compound 1 (Cancer Letters, 70 (1993) 1-6), was assessed in normal as well as in Ehrlich ascites carcinoma (EAC), Sarcoma-180 (S-180) and Dalton's lymphoma (DL)-bearing Swiss male mice by measuring drug-induced changes in (1) hematological parameters and (2) femoral bone marrow cellularity on day 9 following drug treatment at the optimum dose of 3.0 mg/kg body weight from days 1 to 7. Detailed studies were also made by noting sequential changes in the above parameters in normal and EAC-bearing mice on days 12, 15, 18 and 21, respectively. The results indicate that the compound did not adversely affect hematopoiesis. From the sequential studies, it was observed that after a mild initial decrease in hematological counts, particularly in EAC-bearing treated mice, normalcy was reached within 11-14 days after termination of drug therapy. Drug induced hepatotoxicity and nephrotoxicity were also sequentially evaluated in normal and EAC-bearing mice on days 9, 12 and 15 but no such toxicities were detected. Also, body weight, skin and hair texture, and behavioural pattern (food and water intake and activity) did not reflect any toxic reaction in the host mice at this optimum dose.


Subject(s)
Antineoplastic Agents/toxicity , Hydantoins/toxicity , Nitrogen Mustard Compounds/toxicity , Alanine Transaminase/blood , Alkaline Phosphatase/blood , Animals , Aspartate Aminotransferases/blood , Blood Urea Nitrogen , Body Weight/drug effects , Bone Marrow/drug effects , Bone Marrow Cells , Chemical and Drug Induced Liver Injury , Drug Evaluation, Preclinical , Erythrocyte Count/drug effects , Femur , Hemoglobins/metabolism , Kidney Diseases/chemically induced , Kidney Diseases/enzymology , Leukocyte Count/drug effects , Liver Diseases/enzymology , Male , Mice , Platelet Count/drug effects , Thrombocytosis/chemically induced
9.
Indian Pediatr ; 30(3): 351-4, 1993 Mar.
Article in English | MEDLINE | ID: mdl-8365786

ABSTRACT

A study was conducted in selected blocks of West Bengal to assess the utilization of available maternal health services specially immunization, antenatal care and other services. Coverage with two doses of tetanus toxoid levels varied between 58.6 to 86.7% but it fell far short of Universal Immunization Programme target of 100%. Drop out rates were slightly higher in the rural areas. It was observed that in 5 out of 7 blocks more than 55% of the deliveries were conducted either at hospital or Primary Health Centre by health personnel. However, untrained dais predominated over the trained dais in conducting deliveries in most of the areas. This indicates the poor availability or utilization of the latter.


PIP: Between January and September 1990 in India, medical officers trained in the Universal Immunization Programme and paramedics interviewed 1458 women from 7 rural and urban blocks in northern and southern West Bengal to determine utilization of immunization and prenatal care services by pregnant women and to learn where they delivered and who attended the deliveries. The coverage of pregnant women with 2 doses of tetanus toxoid ranged from 58.6% in Hilli block to 86.7% in North Calcutta. Poor information, education, and communication activities in Hilli likely explained the low coverage. The block with the highest percentage of tetanus toxoid dropouts was Mogra block of Hooghly district (11.3%). The lowest percentage of dropouts occurred in Greater Calcutta (Dhakuria) (3.3%). Institutional deliveries were more common in Calcutta (88.1% in North Calcutta and 69.5% in Dhakuria) than the other blocks (e.g., 38.5% in Hilli). The women in the Calcutta blocks to closer to teaching and nonteaching hospitals and private nursing homes than those in the other blocks. Health personnel attended more than 55% of deliveries in all blocks except Hilli (38.5%) and Tamluk (5.9%). The percentage of health personnel deliveries was especially high in Dhakuria (88.5%) and North Calcutta (69.6%). Untrained traditional birth attendants (dais) were present at a higher percentage of deliveries than were trained dais in all blocks, suggesting poor availability or utilization of trained dais. Untrained dais or other untrained people were present at most deliveries (87.6%) in Tamluk. The study only examined utilization of prenatal care services in 4 blocks. The percent using these services was 81.1% in Mogra, 73.9% in Pandua, 61.4% in Balurghat, and 54.9% in Tamluk.


Subject(s)
Maternal Health Services/statistics & numerical data , Female , Humans , Immunization/statistics & numerical data , India , Pregnancy
10.
J Mol Biol ; 218(1): 21-2, 1991 Mar 05.
Article in English | MEDLINE | ID: mdl-2002505

ABSTRACT

Single crystals of the glycosylated inhibitor of cathepsin D and trypsin isolated from potato tubers were obtained using the hanging drop vapor diffusion method and ammonium nitrate as precipitant. The crystals exhibit strong F222 pseudo symmetry but belong to the orthorhombic space group C222 or C222(1), with cell parameters a = 73.8 A, b = 119.9 A and c = 133.2 A with two molecules per asymmetric unit. The crystals diffract to a resolution of 2.4 A.


Subject(s)
Cathepsin D/antagonists & inhibitors , Plant Proteins , Proteins/chemistry , Solanum tuberosum , Crystallization , Freeze Drying , Protein Conformation , Proteins/isolation & purification , X-Ray Diffraction
11.
J Pharmacol Exp Ther ; 240(1): 196-202, 1987 Jan.
Article in English | MEDLINE | ID: mdl-3468240

ABSTRACT

Development of a contingent tolerance to amphetamine (AMPH) anorexia has been reported with chronic s.c. injections in rats (Ghosh and Parvathy, 1973, 1976). Using this model, the present study examined the role of potential receptor sensitivity changes in the beta adrenergic and/or dopamine (DA) receptors in the perifornical hypothalamus (PFH) during chronic central and peripheral drug injections. Chronic injections of AMPH into the PFH, or l-dopa injected s.c., resulted in persistent anorexia in the daily first 2 hr of eating on all test days compared with the next 2 hr that showed a progressive increase in eating with subsequent injections, the net effect being an apparent tolerance to its 4 hr anorexic effect. The tolerance patterns obtained with these two treatments were essentially the same as that of s.c. AMPH, suggesting a role for PFH catecholamine synapses, particularly at the postsynaptic receptor level. Selective beta adrenoceptor-mediated anorexia, as obtained with chronic PFH-injected nor-adrenaline and isoprenaline, was dose-dependent and persistent on all days, suggesting that no change in the sensitivity of PFH beta adrenoceptors had occurred. This contrasted with the PFH-injected DA, which produced a rapid tolerance development due to a progressive loss of effect in the first 2 hr. Present findings suggest that although beta adrenergic and DA mechanisms act in concert in eliciting the acute anorexic effects of AMPH, DA, rather than beta adrenergic system, has a predominant influence in the development of tolerance to the anorexic effect of AMPH.


Subject(s)
Amphetamine/pharmacology , Anorexia/physiopathology , Feeding and Eating Disorders/physiopathology , Hypothalamus/metabolism , Receptors, Dopamine/metabolism , Animals , Anorexia/chemically induced , Benserazide/pharmacology , Dextroamphetamine/pharmacology , Drug Tolerance , Eating/drug effects , Isoproterenol/pharmacology , Levodopa , Male , Rats , Rats, Inbred Strains
12.
Life Sci ; 37(7): 635-43, 1985 Aug 19.
Article in English | MEDLINE | ID: mdl-3927095

ABSTRACT

Tolerance to the anorexic effect of d-amphetamine was studied in rats with selective dopamine lesions in the forebrain by means of 6-hydroxy dopamine, and measuring the food intake during two consecutive 2 h periods. Lesions placed in the perifornical hypothalamus (PFH) strongly antagonised the anorexic effect, whereas, lesions produced via intraventricular injections affected the anorexia only marginally. Amphetamine anorexia observed in the first 2 h in control and lesioned groups remained persistently, without any evidence of tolerance, up to 2 weeks of treatment. The second 2 h food intake exhibited a progressive increase which contributed to the apparent tolerance seen in total 4 h food intake in the control and lesioned animals. The onset and completion of this apparent tolerance was markedly delayed in the dopamine depleted group; lesions placed in the relatively medial areas delayed the tolerance development more effectively than that of PFH lesions. The stimulant effect of amphetamine on locomotion was abolished in lesioned animals. The results indicate that an apparent tolerance to amphetamine anorexia still developed in animals with forebrain dopamine loss. Although both the beta adrenergic and dopaminergic systems act together in mediating AMPH anorexia, the onset and the rate of completion of tolerance appear to be under the influence of hypothalamic dopaminergic system.


Subject(s)
Anorexia/chemically induced , Dextroamphetamine , Dopamine/physiology , Feeding and Eating Disorders/chemically induced , Hypothalamus/physiology , Animals , Body Weight , Drug Tolerance , Energy Intake , Humans , Hydroxydopamines/pharmacology , Male , Oxidopamine , Rats , Rats, Inbred Strains , Time Factors
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