Indian Journal of Biochemistry 
& Biophysics  

Total visitors: 2,340  since 09-12-05

 

ISSN : 0301-1208

CODEN : IJBBBQ  

VOLUME 42

NUMBER 6

DECEMBER 2005

 

 

CONTENTS

 

Papers

 

Overexpression and characterization of a novel chitinase gene from a marine bacterium Pseudomonas sp. BK1 

339

      Moon-Sun Jang, Young-Mi Lee, Young-Su Cho, Yong-Lark Choi, Cherol-Ho Kim and Young-Choon Lee*

 

 

 

Dietary restriction and triiodothyronine (T3) regulation of malate-aspartate shuttle enzymes in the liver and kidney of mice

345

      Danswrang Goyary and R Sharma*

 

 

 

Production of human single-chain variable fragment (scFv) antibody specific for digoxin by ribosome display

350

      Xiang-Hua Yan and Zi-Rong Xu*

 

 

 

Correlation of HER1/EGFR expression and degree of radiosensitizing effect of the HER1/EGFR-tyrosine kinase inhibitor erlotinib

358

      Jae-Chul Kim, M Aktar Ali, Animesh Nandi, Partha Mukhopadhyay,  Hak Choy, Carolyn Cao and Debabrata Saha*

 

 

 

Expression of DΉ-pyrroline-5-carboxylate synthetase gene during drought in rice

      (Oryza sativa L.)

366

      N L Choudhary, R K Sairam and A Tyagi*

 

 

 

Induction of resistance in host against the infection of leaf blight pathogen

      (Alternaria palandui) in onion (Allium cepa var aggregatum)

371

      M Karthikeyan*, V Jayakumar, K Radhika, R Bhaskaran, R Velazhahan and D Alice

 

 

 

Energy barriers and rates of tautomeric transitions in DNA bases: Ab initio quantum chemical study

378

      Soumalee Basu, Rabi Majumdar, Gourab K Das and Dhananjay Bhattacharyya*

 

 

 

Reaction of substituted pyrimidines with photochemically generated t-BuO• radicals

386

      L Charitha and M Adinarayana*

 

 

 

Notes

 

Determination of serum glucose using co-immobilized glucose oxidase and peroxidase on to arylamine glass beads affixed on a plastic strip

391

      Neelima Tank, Suman and C S Pundir*

 

Antibacterial activity of crude methanolic extract and its fractions of aerial parts of Anthemis tinctoria

395

      Cahit Akgul* and Gulsen Saglikoglu

 

 

 

Antibacterial activity of some unsymmetrical diorganyltellurium(IV) dichlorides

398

      Daya Soni, Prabhat K Gupta*, Yatindra Kumar and T G Chandrashekhar

 

 

 

Lead levels in some biological samples of auto-mechanics in Abeokuta, Nigeria

401

      O O Babalola*, L O Ojo and M O Aderemi

 

 

 

Annual Author Index

404

 

 

Annual Subject Index

406

 

 

List of Referees

420

 

 

Instructions to Authors

423

 

 

——————

*Author for correspondence

 

 


AUTHOR INDEX

 

Cho Young-Su

339

Choi Yong-Lark

339

Jang Moon-Sun

339

Kim Cherol-Ho

339

Lee Young-Mi

339

Lee Young-Choon

339

Goyary D

345

Sharma R

345

Xu Zi-Rong

350

Yan Xiang-Hua

350

Ali M A

358

Cao C

358

Choy H

358

Kim Jae-Chul

358

Mukhopadhyay P

358

Nandi A

358

Saha D

358

Choudhary N L

366

Sairam R K

366

Tyagi A

366

Alice D

371

Bhaskaran R

371

Jayakumar V

371

Karthikeyan M 

371

Radhika K

371

Velazhahan R

371

Basu S

378

Bhattacharyya D

378

Das G K

378

Majumdar R

378

Adinarayana M

386

Charitha L

386

Pundir C S

391

Suman

391

Tank N

391

Akgul C

395

Saglikoglu G

395

Chandrashekhar T G

398

Gupta P K

398

Kumar Y

398

Soni D

398

Aderemi M O

401

Babalola O O

401

Ojo L O

401


 

 

 

 

Papers

 

Indian Journal of Biochemistry & Biophysics

Vol. 42, December 2005, pp. 339-344

 

Overexpression and characterization of a novel chitinase gene from a marine bacterium Pseudomonas sp. BK1 

Moon-Sun Jang, Young-Mi Lee, Young-Su Cho, Yong-Lark Choi, Cherol-Ho Kim1 and Young-Choon Lee*

 

The chitinase A (ChiA)-coding gene of Pseudomonas sp. BK1, which was isolated from a marine red alga Porphyra dentata, was cloned and expressed in Escherichia coli. The structural gene consists of 1602 bp encoding a protein of 534 amino acids, with a predicted molecular weight of 55,370 Da. The deduced amino acid sequence of ChiA showed low identity (less than 32%) with other bacterial chitinases. The ChiA was composed of multiple domains, unlike the arrangement of domains in other bacterial chitinases. Recombinant ChiA overproduced as inclusion bodies was solubilized in the presence of 8 M urea, purified in a urea-denatured form and re-folded by removing urea. The purified enzyme showed maximum activity at pH 5.0 and 40°C. It exhibited high activity towards glycol chitosan and glycol chitin, and lower activity towards colloidal chitin. The enzyme hydrolyzed the oligosaccharides from (GlcNAc)4 to (GlcNAc)6, but not GlcNAc to (GlcNAc)3. The results suggest that the ChiA is a novel enzyme, with different domain structure and action mode from bacterial family 18 chitinases.

Keywords: Pseudomonas, chitinase, cloning, overexpression, refolding

 

IPC Code: C12N15/52; C12N9/28

          E -mail:  yclee@dau.ac.kr

 

 

Indian Journal of Biochemistry & Biophysics

Vol. 42, December 2005, pp. 345-349

 

Dietary restriction and triiodothyronine (T3) regulation of malate-aspartate shuttle enzymes in the liver and kidney of mice

Danswrang Goyary and R Sharma*

 

The activities of malate-aspartate shuttle enzymes viz., cytosolic and mitochondrial aspartate aminotransferase (c- and m-AsAT) and malate dehydrogenase (c- and m-MDH) were measured in liver and kidney of ad libitum (AL) and dietary- restricted (DR) mice and also on triiodothyronine (T3) treatment. The results show that the activity (U/mg protein) of c-AsAT is increased significantly in liver and the activities of c-MDH and m-AsAT are increased significantly in kidney during DR. On T3 treatment, the activities of both the isoenzymes (c- and m-) of MDH and AsAT are increased significantly in the liver of AL- and DR-fed mice. In the kidney, m-MDH showed no effect by T3 treatment, however, c-MDH increased significantly in both AL- and DR-fed mice. In contrast, m-AsAT is increased significantly in the kidney in AL-fed mice, but was not affected in DR-fed animals. In vitro reconstitution of malate-aspartate shuttle showed a higher activity in the liver and kidney of DR-fed mice, as compared to AL-fed ones and also in the T3-treated mice, compared to untreated ones. These findings suggest that malate-aspartate shuttle enzymes are differentially regulated during DR in mice, in order to adapt to the metabolic need of liver and kidney. T3 potentially regulates the shuttle enzymes, albeit to a varying degree in the liver and kidney of AL- and DR-fed mice.

Keywords: Malate-aspartate shuttle enzymes, dietary restriction, triiodothyronine (T3), liver, kidney, mice.

          E-Mail: rsharma@nehu.ac.in

 

 

 

Indian Journal of Biochemistry & Biophysics

Vol. 42, December 2005, pp. 350-357

 

Production of human single-chain variable fragment (scFv) antibody specific for digoxin by ribosome display

Xiang-Hua Yan and Zi-Rong Xu *

 

Ribosome display was applied in vitro to select single-chain variable fragment (scFv) antibody specific for digoxin from a human non-immune naive scFv library. A cell-free system was used to produce stable antibody-ribosome-mRNA (ARM) complexes to provide the linkage of genotype and phenotype, allowing simultaneous selection of a desired antibody together with its encoding mRNA. The mRNA was then recovered and amplified as DNA by reverse transcriptase-polymerase chain reaction (RT-PCR). Repeating the display cycle enriched the selected molecules, enabling rare species to be isolated. In this study, digoxin-binding segments were selected over four cycles of ARM display and the selected DNA was cloned and expressed as a single-chain variable fragment antibody (the best scFv, A3) in Escherichia coli. The affinity (equilibrium dissociation constant Kd) of digoxin was 8.3 Χ 10-8 M for A3, which validated construction of the naοve library and the power of ribosome display lending to the evolution of functional characteristics, such as potency of leading candidate antibodies to provide therapeutic antibodies. A3 was purified using affinity chromatography and determined by Western blot. The results indicate that ribosome display technnique can be efficiently used to isolate specific antibody fragments from a naive library.

Keywords: Single-chain Fv, ribosome display, non-immune libraries, digoxin

IPC Code: C07J19/00

          E-Mail: xhyan@zju.edu.cn; yanxiangh@sina.com

 

 

 

 

Indian Journal of Biochemistry & Biophysics

Vol. 42, December 2005, pp. 358-365

 

Correlation of HER1/EGFR expression and degree of radiosensitizing effect of the HER1/EGFR-tyrosine kinase inhibitor erlotinib

Jae-Chul Kim¨, M Aktar Ali, Animesh Nandi, Partha Mukhopadhyay, Hak Choy, Carolyn Cao and Debabrata Saha*

 

Epidermal growth factor receptor (HER1/EGFR)-mediated signal transduction pathways are important in cellular response to ionizing radiation. High HER1/EGFR expression on cancer cells may contribute to radioresistance. In this pre-clinical study, we evaluated the radiosensitizing effect of erlotinib, a small molecule HER1/EGFR inhibitor in three human cancer cell lines with different HER1/EGFR expression — A431 (very high expression), H157 (moderate expression) and H460 (low expression). Our results demonstrated that A431 was the most radioresistant, while H460 was the most radiosensitive. However, A431 cells were the most sensitive to erlotinib (IC50 = 300 nM) and H460 cells the most resistant (IC50 = 8 mM). H157 had intermediate sensitivity to radiation and erlotinib (IC50 = 3 mM). With 300 nM erlotinib, the radiation dose enhancement ratios (DER) were 1.40, 1.17 and 1.04 in A431, H157 and H460, respectively. Treatment with erlotinib for 24 hr at 300 nM increased G1 arrest by 18.6, 2.0 and 4.8% in A431, H157 and H460, respectively. Erlotinib-induced apoptosis was augmented by radiation in A431 cells only. In conclusion, high HER1/EGFR expression may result in a high degree of radiosensitization with erlotinib combined with radiation. The extent of erlotinib-induced radiosensitization was proportional to HER1/EGFR expression, as well as autophosphorylation of the human epidermal growth factor receptor (HER1/EGFR).

Keywords: Epidermal growth factor (EGF), erlotinib, HER1/EGFR inhibitor, HER1/EGFR expression, radiosensitization, autophosphorylation, lung cancer, cell lines A431, H157 and H460, flow cytometric analysis, cell cycle analysis, apoptosis, tyrosine kinase activity

IPC Code: C12N 15/52

         E-Mail:  debabrata.saha@utsouthwestern.edu

 

 

 

Indian Journal of Biochemistry & Biophysics

Vol. 42, December 2005, pp. 366-370

 

Expression of DΉ-pyrroline-5-carboxylate synthetase gene during drought in rice (Oryza sativa L.)

N L Choudhary1, R K Sairam2 and A Tyagi1*

 

The 45-days-old seedlings of drought resistant (N-22, CR143-2-2) and susceptible rice (Oryza sativa L.) genotypes (Panidhan, Pusa-169) were subjected to osmotic stress in PEG-6000 solution of -10 and -16 bar and the relative water content (RWC), proline content, and pyrroline-5-carboxylate synthetase (P5CS) activity and its P5CS expression were studied. A gradual decrease in RWC was observed in tolerant genotypes, whereas the decrease was drastic in susceptible ones. Proline content and P5CS activity increased both in susceptible and tolerant genotypes; the increase was higher in tolerant genotypes. Higher proline levels in tolerant genotypes were due to increased P5CS activity. The EcoRI, BamHI and XbaI restricted DNA of N-22 and Panidhan genotypes were hybridized with Arabidopsis P5CS sequence and a single band (approx 2.4 kb) was observed, however, P5CS expression was more in N-22, as compared to Panidhan.

Keywords: Rice, Oryza sativa L., osmotic stress, proline, pyrroline-5-carboxylate synthetase, P5CS expression,
relative water content

IPC Code: C12Q1/00, C12N15/52

          E-Mail: at_bio@iari.res.in

 

 

 

Indian Journal of Biochemistry & Biophysics

Vol. 42, December 2005, pp. 371-377

 

Induction of resistance in host against the infection of leaf blight pathogen (Alternaria palandui) in onion (Allium cepa var aggregatum)

M Karthikeyan*, V Jayakumar1, K Radhika2, R Bhaskaran3, R Velazhahan and D Alice

 

The Pseudomonas fluorescens isolate Pf1 was found to inhibit the growth of pathogen Alternaria palandui, in vitro. In the present study, foliar application of a talc-based formulation of Pf1 significantly reduced the incidence of leaf blight of onion, caused by A. palandui. Induction of defense-related proteins viz., chitinase, b-1,3 glucanase, peroxidase (PO) and polyphenol oxidase (PPO) by application of Pf1, was studied against A. palandui infection in resistant (IHR 56) and susceptible (MDU1) onion cultivars. Chitinase in both cultivars, with or without challenge-inoculation of A. palandui revealed changes in the isoform pattern. The Native-PAGE of PO showed induction of PO2 isoform in both the cultivars, in response to inoculation of pathogen. Isoform analysis of PPO also exhibited  induction in the Pf1-treated plants challenged with pathogen. Similarly, the activity of b-1,3-glucanase was greatly induced in Pf1-treated plants, challenged with pathogen as compared to controls. Thus, the P. fluorescens-treated plants showed significant increase in the levels of the defense enzymes, in comparison to the plants challenged with the pathogen.

Keywords:     Leaf blight, onion, Alternaria palandui, Pseudomonas fluorescens, induced systemic resistance, defense-related proteins, chitinase, b-1,3 glucanase, peroxidase, polyphenol oxidase

IPC Code:     C12R1/39, C12Q1/28

          E-Mail: karthipath@rediffmail.com

 

 

 

Indian Journal of Biochemistry & Biophysics

Vol. 42, December 2005, pp: 378-385

 

Energy barriers and rates of tautomeric transitions in DNA bases:
Ab initio quantum chemical study

 

Soumalee Basu1$, Rabi Majumdar1, Gourab K Das2 and Dhananjay Bhattacharyya3*

 

Tautomeric transitions of DNA bases are proton transfer reactions, which are important in biology. These reactions are involved in spontaneous point mutations of the genetic material. In the present study, intrinsic reaction coordinates (IRC) analyses through ab initio quantum chemical calculations have been carried out for the individual DNA bases A, T, G, C and also A:T and G:C base pairs to estimate the kinetic and thermodynamic barriers using MP2/6-31G** method for tautomeric transitions. Relatively higher values of kinetic barriers (about 50-60 kcal/mol) have been observed for the single bases, indicating that tautomeric alterations of isolated single bases are quite unlikely. On the other hand, relatively lower values of the kinetic barriers (about 20-25 kcal/mol) for the DNA base pairs A:T and G:C clearly suggest that the tautomeric shifts are much more favorable in DNA base pairs than in isolated single bases. The unusual base pairing A′:C, T′:G, C′:A or G′:T in the daughter DNA molecule, resulting from a parent DNA molecule with tautomeric shifts, is found to be stable enough to result in a mutation. The transition rate constants for the single DNA bases in addition to the base pairs are also calculated by computing the free energy differences between the transition states and the reactants.

Keywords: Tautomerism, DNA, spontaneous mutation, quantum chemistry, transition rate, unusual base pairing, intrinsic reaction coordinate analysis

IPC Code: C07H21/04

          E-Mail:  dhananjay.bhattacharyya@saha.ac.in

 

 

 

Indian Journal of Biochemistry & Biophysics

Vol. 42, December 2005, pp. 386-390

 

 

Reaction of substituted pyrimidines with photochemically generated
t-BuO• radicals

L Charitha and M Adinarayana*

Humans are exposed to various organic peroxides through chemical, pharmaceutical and cosmetic products. On photolysis, these peroxides produce alkoxyl radicals and hydroxyl radicals. The reaction of ·OH radicals with DNA and its constituents have been extensively studied, but very little is known about the reactions of alkoxyl radicals with DNA and its constituents. In view of this, the oxidation of pyrimidine bases viz., thymine, uracil, cytosine, 5-bromouracil, 6-methyluracil and 1, 3-dimethyluracil by t-BuO· radicals in aqueous solution at pH 7.5 has been carried out. The reaction between pyrimidine and t-BuO· is followed by measuring the absorbance of pyrimidine at the respective lmax. The rates of oxidation of pyrimidines are calculated from the plot of absorbance vs time. The rates of oxidation of pyrimidines have been found to increase with increase in [t-BuOOH], [pyrimidine] and light intensity. The quantum yields are calculated from the initial rates of oxidation of pyrimidine and the measured light intensity at 254 nm the wavelength at which t-BuOOH is activated to give radicals. The quantum yields are found to depend on [pyrimidine] as well as on [t-BuOOH] while they are independent of light intensity. The product analysis was carried out on HPLC with UV-visible detector. The corresponding 5,6-dihydroxypyrimidine and isobarbituric acid have been identified by comparing the retention times of the authentic samples. On the basis of experimental results and product analysis, it is suggested that t-BuOOH on photolysis gives t-BuO· radical, which initiates the reaction by adding to C (5) or C (6) position of pyrimidine base, leading to the formation of pyrimidine base radical via hydrolysis. The pyrimidine radical further reacts with t-BuO· radical to give the final product. This study predicts the probable transient pyrimidine radicals.

Keywords: tert-butyl hydroperoxide, t-BuO· radical, pyrimidine bases, oxidation of pyrimidines by t-BuO

·

IPC Code: C07D 239/00, C07H 1906

         E-Mail:  mundra_adinarayana@hotmail.com

 

 

 

Notes

Indian Journal of Biochemistry & Biophysics

Vol. 42, December 2005, pp. 391-394

 

Determination of serum glucose using co-immobilized glucose oxidase and peroxidase onto arylamine glass beads affixed on a plastic strip

Neelima Tank, Suman and C S Pundir*

 

Glucose oxidase (GOD) from Aspergillus niger and horseradish peroxidase (POD) were co-immobilized onto arylamine glass beads affixed on a plastic strip with a conjugation yield of 28.2 mg/g and 43% retention of their initial specific activity. The co-immobilized enzymes showed maximum activity at pH 7.5 when incubated at 37°C for 15 min. A simple, specific and sensitive method for discrete analysis of the serum glucose was developed employing this strip. The minimum detection limit of the method was 5 mg/dl. Within and between assay coefficient of variations for the serum were <5.6% and <10.6% (n = 6) respondely. A good correlation (r = 0.943) was found between the glucose values obtained by the enzyme colorimetric method employing free GOD and POD and the present method. The strip lost 50% of its initial activity after its 150 regular uses for a period of one month, when stored in reaction buffer at 4°C. The method is cost-effective than the enzymic colorimetric method, as the enzyme strip is reusable

          Keywords: Glucose determination, glucose oxidase, peroxidase, arylamine glass, co-immobilization, serum, plastic strip.

IPC Code: C12N 11/00

          E-Mail: pundircs@rediffmail.com

 

 

 

 

Indian Journal of Biochemistry & Biophysics

Vol. 42, December 2005, pp. 395-397

 

Antibacterial activity of crude methanolic extract and its fractions of aerial parts of Anthemis tinctoria

Cahit Akgul* and Gulsen Saglikoglu

 

The antibacterial activity of the methanolic extract and its fractions of aerial parts of Anthemis tinctoria (Asteraceae) was investigated against representative gram-positive Staphylococcus aureus (ATCC 25923) and Enterococcus faecalis (ATCC 29212) and gram-negative strains Escherichia coli (ATCC 25922) and Pseudomonas aeruginosa (ATCC 27853). The activity was concentrated mainly in the dichloromethane (DCM) and hexane fractions of crude methanolic extract. The 5 mg of DCM extract per disk produced 15-16 mm of inhibition zone against S. aureus and P. aeruginosa, however, no activity was found against E. faecalis and E. coli. The hexane fraction showed activity against S. aureus, P. aeruginosa and E. faecalis. As DCM fraction showed the highest antibacterial activity in the disk diffusion assay, the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) values of only this fraction was determined against S. aureus and P. aeruginosa. These values were found to be in the range of 1.25 to 10 mg/ml.

          Keywords: Anthemis tinctoria, antibacterial activity, Pseudo-monas aeruginosa, Staphylococcus aureus, MIC, MBC

IPC Code: A61P31/04

          E-Mail: cahitakgul@comu.edu.tr; cahitakgul@yahoo.com

 

 

 

 

 

Indian Journal of Biochemistry & Biophysics

Vol. 42, December 2005, pp. 398-400

 

Antibacterial activity of some unsymmetrical diorganyltellurium(IV) dichlorides

Daya Soni, Prabhat K Gupta*, Yatindra Kumar# andT G Chandrashekhar#

 

Six unsymmetrical diorganyltellurium(IV) dichlorides RR'TeCl2 (where R= phenacyl-, 1-naphthacyl-, and styrylacyl- and R' = p-methoxyphenyl, p-hydroxyphenyl-, and 3-methyl-4-hydoxyphenyl-) were tested for their antibacterial activity against gram-positive (Bacillus subtilis ATCC 6633 and Staphylococcus aureus ATCC 25923) and gram-negative (Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853 and Salmonella sp.) bacteria. Antibacterial activity was measured by disk diffusion method. Inhibition zones demonstrated that all the compounds showed good activity against gram-negative strains. Phenacyl (3-methyl-4-hydroxyphenyl) tellurium(IV) dichloride and naphthacyl (3-methyl-4-hydroxyphenyl) tellurium(IV) dichloride showed significant activity against both gram-positive and gram-negative strains. Among the tested compounds, the former exhibited maximum activity against gram-positive bacteria, while the latter against all the bacteria under study and styrylacyl (p-methoxyphenyl) tellurium(IV) dichloride against all the three gram-negative bacteria.

        Keywords: Unsymmetrical diorganyltellurium(IV) dichlorides, antibacterial activity, Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Salmonella sp.

IPC Code: C12Q1/18

         E-Mail:  prabhat@mail.nplindia.ernet.in; dsoni@mail.nplindia.ernet.in

 

 

 

 

Indian Journal of Biochemistry & Biophysics

Vol. 42, December 2005, pp. 401-403

 

Lead levels in some biological samples of auto-mechanics in Abeokuta, Nigeria

O O Babalola*, L O Ojo and M O Aderemi

 

Lead levels were determined in the blood, scalp hair and fingernails of 38, all male auto-mechanics (aged 18-45 years) from Abeokuta, South-western Nigeria. The subjects were classified into four sub-groups based on the period of exposure namely: 1-5, 6-10, 11–15, and >16 years. Thirty-two occupationally unexposed subjects (mainly office workers) served as the control. The weight, height and body mass indexes of all subjects were noted, in addition to other information obtained through structured questionnaire. The mean values of blood lead (BPb), hair lead (HPb) and fingernail lead (NPb) of the occupationally exposed subjects (n=38) were 48.50 ± 9.08 mg/dL, 17.75 ± 5.16 mg/g, and 5.92 ± 3.30 mg/g respectively, while the corresponding mean values for these parameters in the control subjects (n = 32) were 33.65 ± 10.09 mg/dL, 14.30 ± 5.90 mg/g and 5.31 ± 2.77 mg/g respectively. The differences in BPb and HPb levels of the two groups were statistically significant (P <0.05 and P <0.01 respectively), while that of NPb was not significant. The levels of lead in the biological samples appeared to have no relationship with the number of years on the job. From these results, it was obvious that the higher levels of lead in the biological samples of test subjects, compared with those of the controls were from environmental sources.

          Keywords:   Lead, auto-mechanics, occupationally exposed subject, blood, fingernail, hair

IPC Code:      G01N33/00

          E-Mail: segunbablo@yahoo.ca

 

 

      

 


Annual Author Index

 

Abraham P

59

Aderemi M O

401

Adinarayana M

386

Aggarwal L M

127

Aggarwal S

113

Ahlawat S P S

173

Akgul C

395

Ali M A

358

Alice D

371

Anand A

122

Aslan S

190

Babalola O O

401

Balasaraswathi R

228

Basu S

378

Behere D V

7

Behl R

173

Bhadauria M

321

Bhaskaran R

371

Bhatia S

152

Bhattacharyya D

378

Bhide S V

156

Biswas S

145

Cao C

358

Chakrabarti J

238

Chakrabartty P K

287

Chakrabarty R

243

Chakraborti S

19

Chakraborti T

19

Chakraborty S

106

Chandrashekhar T G

398

Charitha L

386

Chatterjee A

205

Chen J

100

Cheng X

166

Chimni S S

233

Cho Young-Su

339

Choi Yong-Lark

339

Choudhary N L

366

Choudhury R

19

Choy H

358

Dahot M U

326

Darbari R

127

Das G K

378

Das K P

287

Das S

238

De M

287

Demir N

182

Demir Y

182

Dhingra J B

173

Dubey R K

301

Dubey R

73

Forouzandeh M

113

Gagandeep

216

Gao Z Q

41

Ge H

222

Ge S

166

Geraldine P

258

Ghasemi S

326

Ghosh B

19

Ghosh Z

238

Gφnenη A

190

Gopal G

81, 271

Goyary D

345

Gupta A K

161, 315

Gupta Anil K

295

Gupta P K

398

Gupta R

233

Hutchinson T E

92

Indra C

13

Irshad M

73

Jabeen T

279

Jadon A

321

Jain P

315

Jang Moon-Sun

339

Jawed A

233

Jayakumar V

371

Jethi R K

113

Josephrajkumar A

243

Joshi D K

122

Kale R K

216

Kamal J K A

7

Kamboj S S

34

Kanwar S S

233

Karthikeyan M

371

Kashkedikar S G

315

Katyare S S

48

Kaur A

34

Kaur H

295

Kaur M

34

Kaur N

161, 295

Kaur P

161, 279

Kaushal R K

233

Kestwal R M

156

Kim Cherol-Ho

339

Kim Jae-Chul

358

Kiran R

113

Kong X

222

Kumar Y

398

Lee Young-Choon

339

Lee Young-Mi

339

Li M

222

Liu J

308

Liu Q

100

Liu W

100

Liu X

100

Liu Z

222

Lodha M L

152

Majumdar R

378

Mallick B

238

Mandal A

19

Manivasagam T

87

Mehta A

54, 254

Mitra C K

141

Moulik S P

205

Mukhopadhyay P

358

Nagarajan S

122

Nandi A

358

Ojo L O

401

Pandya J D

48

Pathak P C

122

Patil N D

250

Pavan Y S

141

Pereira Ben M J

92

Prakash P

118

Prasad S K

173

Pundir C S

186, 391

Qin S

308

Radhika K

371

Rai D V

127

Rajalekshmy R

271

Rajesh M

13

Rajkumar T

81, 271

Ramakrishnan S 

13

Rao A R

216

Rastogi A

92

Reshamwala S M S

250

Roy K

106

Saboury A A

326

Saglikoglu G

395

Saha D

358

Sairam R K

366

Saxena A K

34

Selvaluxmi G

271

Selvaraju K

228

Sengupta C

106

Shanju S

258

Shanmugasundaram P

228

Sharma A

145

Sharma Anjana

178

Sharma R

345

Sharma S

279

Shukla S

321

Shyamala Devi C S

246

Singh J

34

Singh Jagmohan

34

Singh R K

279

Singh T P

279

Singla S K

113

Sinha S

228

Soni D

398

Soni L K

315

Sood S K

34

Srinivasan A

279

Srinivasan V

13

Sritharan M

28

Srivastava N

54, 254

Subramanian P

87

Suchalatha S

246

Sulochana K N

13

Suman

186, 391

Sundaram C A S S

28

Suthakar G

87

 

 

Tandon C

113

Tank N

391

Thomas G

243

Tiwari R

178

Tokgφz D

190

Torun M

190

Tripathi D N

301

Tripathi O

118

Tseng C K

41

Tyagi A

366

Velazhahan R

371

Verma A P S

122

Verma N K

173

Verma R S

54, 254

Wang G C

41

Xu X

100

Xu Zi-Rong

350

Xue Z

166

Yan Xiang-Hua

350

Yang L

166

Yeruva V C

28

Yildirim S

182

Zheng W

222

Zheng X

166

 

Annual Subject Index

 


A

abdominal gases, cardamom in reduction of 245

abiotic stress   295

abscisic acid (ABA)        295
inhibitory effect of               297

N-Acetylchitooligosaccharides, enzymatic
   hydrolysis of                  341

acetylcholine esterase      145
chlorpyrifos-induced alterations in rat brain       54–57
inhibition of 254

acromegaly      76

actin dynamics in monocytes, changes in     13

action potential 118

Acutolysin A, from Agkistrodon acutus, effects
   of metal ions and EDTA on fluorescence and
   caseinolytic activity of    100

adenocarcinoma           271, 324

Adenosine triphosphatase (ATPase)
activity, assay of                 251
activity in pulmonary artery smooth muscle
   microsomes, stimulation by t-butylhydroperoxide                19
chlorpyrifos-induced alterations in rat brain       54–57
cleaving and release by PLC-Bc                92

Aeromonas spp., chitinases from                  343

affinity chromatography, concanavalin A
   CL seralose                  156

Age-related changes in elemental constituents
   and molecular behaviour of bone   
127–129

Aging               77

Agkistrodon acutus, acutolysin A from    100–104

agonists, in inducing hydrolysis of
   phosphatidylinositol-4,5-diphosphate 173

AIDS patients
fatal opportunistic pathogens in 315
immunocomprised                320

alanine, in modulating IRTK and PI3K activities
   and on changes in actin dynamics in monocytes
   (MC), exposed to high glucose concentration 13–18

Alfa feto protein (AFP)           73

alga, Porphyra yezoensis, improved method for
   isolation of photosystem II from             41

alkaline phosphatase
assay of       94
from Elephas trogontherii (Steppe elephant)
   bone, characterization and purification of       
182–185

alkoxyl radicals 386

alkylamine glass, immobilization of enzyme on to 187

allele-specific oligonucleotide (ASO) 308, 313

Allium cepa var aggregatum, induction of resistance
   against Alternaria palandui infection 371–377

Alternaria palandui infection in onion,
   induction of resistance against           371–377

Alzheimer’s disease                    73

amino acids
antiglycating effect of       13
differential regulation of IRTK and PI3K
   activities in human monocytes 13–18
modulation of enzyme activities in insulin-
   mediated signal transduction pathway  13–18

7-aminoactinomycine-D            358

4-aminoantipyrine                  186

β-Aminobutyric acid (BABA)-mediated enhance-
   ment of resistance in tobacco against TMV
   and capability in wounded tobacco plants           166–171

cAMP, membrane permeable analog of        118–121

 

amplified ribosomal DNA restriction
   analysis (ARDRA)    178

Amplimers   84–85

Amplitron       310

Amylase, from Serratia spp.           178–179

amylase activity in cowpea cotyledons  295
embryo is not required for initiation of  161–165

a-Amylase 161, 295
from Bacillus amyloliquefaciens NCIM 2829,
   purification and characterization of       287–293
extraction, determination and purification of       162, 164
gene expression                 163
magnesium ion binding to, thermodynamic
   study of   326–329

amyloglucosidase                  296

amyloid precursor protein (APP) 73
gene             76

amyloidosis     78
cutaneous      77

anaphase promoting complex (APC)                 271
members of family         276

Anaphylaxis, acute                  350

angoumois grain moth, see Silotraga cereallela

Aniline, for degradation of RNA           153

Anthemis cotula, flowers of, antimicrobial
   activity of 395

Anthemis tinctoria, aerial parts of, antibacterial
   activity of 395–397

Antibacterial activity
methanolic extract and its fractions of aerial
   parts of Anthemis tinctoria     395–397
of some unsymmetrical diorganyltellurium
   (IV) dichlorides  398–400

Antibody library construction 355

antibody-ribosome-mRNA (ARM) complexes   350

antiinflammatory effect, Terminalia chebula fruit 246

antimalarial drug                  145

Antioxidant activity of ethanolic extract of
   Terminalia chebula fruit against iso-
   proterenol-induced oxidative stress in rats 246–248

antioxidant enzymes, specific activities of               216

Antioxidants      19

antiproliferative effect, of Arisaema intermedium
   tubers        34

antitumor activity                  364

Antiviral proteins (AVPs)
from Bougainvillea xbuttiana cv Mahara leaves 
   DNase activity of       152–153
   purification of                 152
MAP   152, 154–155
PAP   152, 155
RNase activity of                 153
on viral RNAs           153, 155

apatite            113

Apis mellifera, propolis from 321

Apolipoproteins
and medical conditions
   acquired disorders 75–78
   inherited disorders      75
physiological changes in levels                   75
role in different clinical conditions 73–78
structural characteristics
   Apo AI, AII, AIV        73, 74
   Apo(a)      75
   Apo B-100 and Apo B-48     74
   Apo C-I, C-II, C-III            74
   Apo E       74
   Apo H 74–75
   Apo J         75

Apolipoproteins and acquired disorders
cancer      75
cardiovascular diseases 75–76
central nervous system (CNS)               75
endocrinological disorder          76–77

Apoptosis 193, 276, 358, 360
induction in PC12 cells exposed to ESA          222–226
measurement of           360–361

aprotinin        243

Arabidopsis spp.
protection against                 171
sugar signaling mutants in   299

Arabidopsis thaliana
osmotic stress                 369
P5CS
of      369

arachidonic acid                  222

Archaeal tRNA genes          238

arginine, in modulating IRTK and PI3K activities
   and on changes in actin dynamics in monocytes
   (MC), exposed to high glucose concentration 13–18

Arisaema intermedium, N-acetyl-D-lactosamine
   specific lectins from tubers of               34–40

Arisaema wallichianum, N-acetyl-D-lactosamine
   specific lectins from tubers of               34–40

ascorbic acid, inhibition of iron-induced lipid
   peroxidation                  247

Asialofetuin       34

aspartate aminotransferase                  345

Aspergillus fumigatus, chitinases from                  343

atherosclerosis 190
risk factor for 77

ATPase, see Adenosine triphosphatase

Austin model-1 316

autoantibodies  77

Autoimmune diseases   77–78

auto-mechanics, lead levels in biological
   samples from           401–403

autophagy by lysosomes   324

Autophosphorylation                  358                  361

AUTOREG, for calculation of E-state index   106

Auxins, in promotion of gibberellin biosynthesis 161

avidin-biotin peroxidase complex      273

 

B

BABA, see β-aminobutyric acid

Bacillus amyloliquefaciens-amylase (BAA)                  326

Bacillus amyloliquefaciens NCIM 2829, a-amylase
   from, purification and characterization of        287–293

Bacillus cereus, PLC-Bc from 92

Bacillus circulans, chitinases of 341

Bacillus coagulans, lipase from  233, 235

Bacillus spp., from effluents of gelatin factory                  179

Bacillus subtilis
strains YY 88 and NRRL B 3411, molecular
   mass of
a-amylase from 292
unsymmetrical diorganyltellurium(IV)
   dichlorides against        398

Bacillus thuringiensis, PLC-Bt from 92

Bacteria
chitinolytic  339
oil-degrading property of  180

bacterial strains, methods for identification of                  178

‘ball and stick’ models, heme binding location
   in human MHA              8

barley, see Hordeum vulgare

base pairing, unusual       378

Base pairs, non-Watson-Crick, stability of   384–385

basis set superposition error (BSSE) 378
correction by Morokuma method       380

Bcl2, indicator of poor prognosis in cervical cancer                  271

Becton Dickinson cell quest FACStation 273

bee glue, see Propolis

benzamidazole, antibacterial activity of    398

benzene, 1-chloro-2,4-dinitro-, (CDNB)      216

benzidine, tetramethyl    28

Benzo(a)pyrene 216

benzoic acid, 5,5'-dithiobis-2-nitro-, (DTNB)      216

benzothiadiazole-7-carbothioic acid S-methyl
   ester (BTH)                  166

benzoyl-arg-p-nitroanilide  243

Bigdye terminator                    83

Biocontrol agent, Pseudomonas fluorescens
   strain Pf1 372

biocontrol and biodegrading agents, Serratia spp.            178

Biopolymers, see Surfactant-biopolymer interaction

biosensors, for determination of lactate, in
   muscles and liver            186

Blast, in rice, Pseudomonas fluorescens
   strain Pf1 against        372

BLASTn search 83–84, 272

Blastocysts      173

Bone
age-related changes in elemental constituents
   and molecular behaviour   
127–129
Steppe elephant, characterization and
   purification of alkaline phosphatase from   
182–185

bone marrow, protection of 315

Bougainvillea xbuttiana, AVPs from leaves of,
   RNase and DNase activities of               152

Box-counting principle      142

brachytherapy 272

brain injury      76

breast cancer   76
   oxidative stress in relation to lipid profiles
   in different stages of 190–193

8-Bromo-cAMP, membrane permeable analog
   of cAMP  118
8-Bromo-cGMP, membrane permeable analog
   of cGMP  118

N-bromosuccinimide                 156

5-bromouracil (5BrU)        388

brown planthopper (BPH), see Nilaparvata lugens

BSSE, see Basis set superposition error

Bulge-Helix-Bulge (BHB)        239

Bulked segregant analysis       231

butylatedhydroxytoluene (BHT) 190                  191

t-BuO• radicals, photochemically generated,
   reaction of substituted pyrimidines with           386–389

t-butylhydroperoxide, stimulation of MMP-2
   and Ca2+-ATPase activity in bovine pulmonary
   artery smooth muscle microsomes by              
19–26

 

C

C33A, cervical cancer cell line                  271

c-erbB2, indicator of poor prognosis in
   cervical cancer                  271

c-myc over-expression, indicator of poor
   prognosis in cervical cancer                  271

Ca2+ channel activity in embryonic myocardium 118–121

Ca2+ uptake in microsomes of bovine pulmonary
   artery smooth muscle
, role of MMP-2 in
   oxidant-mediated regulation of  19–26

Ca2+-ATPase activity in bovine pulmonary artery
   smooth muscle microsomes, stimulation by
   t-butylhydroperoxide treatment  19–26

calcium binding loop     283–284
calcium oxalate monohydrate (COM)
   crystal growth                  113
calculi            113

callose deposition                  166

calphostin-C, PKC inhibitor      150

cAMP, see AMP

camphorin, convertion of supercoiled plasmid
   DNA into linear form  155

Canavalia gladiata (Jack bean), concanavalin A
   from seeds of                  157

cancer             75
breast           76
cervix           81
prostate        76
radiation and chemotherapy of, implications in                216

canonical introns                  238

Capsicum annum, pythium disease of,
  
Pseudomonas fluorescens strain Pf1 against  372

carboxymethyl cellulose      343

carcinogen metabolizing enzymes      216

carcinoma, see specific types

Cardamom, see Elettaria cardamomum

cardiomyocytes 247

Cardiomyopathy                  345

cardioprotective effect of Terminalia chebula
   fruit extract 246

cardiovascular diseases  75–76
prevention by Terminalia chebula fruit extract         248

carob, see Ceratonia siliqua

Carotenoids, in formation of vitellin in
   freshwater prawns        258

Carr-Purcell-Meiboom-Gill (CPMG) method,
   to measure T2 of water protons                  123

caseinolytic activity of acutolysin A from
   Agkistrodon acutus
         101

catalase-peroxidases in mycobacteria, iron
   concentration on expression and activity of               28–32

catechins        248

catechol         248

CD, see Circular dichroism

CDC27
homologue in Schizosaccharomyces pombe 274
protein, involvement in radiation response in
   squamous cell cervix carcinoma           271–277

cDNA, see DNA

cell cycle
analysis 358, 360, 362–363
arrest          276

Cell irradiation  81–82, 273

cell lines
A431, H157 and H460         358
cervical cancer, SiHa and C33A                 271
cervical carcinoma derived, expression of
   mrps28 variant in response to radiation 81–86
human cancer 34

cell membrane thermostability, wheat leaves           122–125

central nervous system (CNS)                75

Ceratonia siliqua seedlings, water-deficit stress in
   cotyledons of                  298

cerebral malaria                  145

cerebro spinal fluid (CSF)          73
Apo E concentration in                    76

ceruloplasmin activity, inhibition of iron induced
   lipid peroxidation 247

cervical cancer, indicators of poor prognosis in                  271

cervical carcinoma derived cell line SiHa             81

cervical tumour cells, down-regulation of CDC27 in    277

cervix cancer    81

cetuximab      363

cetyl diethanolyl methyl ammonium bromides
   (CDMAB), interaction with calf thymus DNA   205–214

cetyl ethanolyl dimethyl ammonium bromides
   (CEDAB), interaction with calf thymus DNA   205–214

cetyl pyridinium chloride (CPC), interaction
   with calf thymus DNA           205–214

cetyl trimethyl ammonium bromides (CTAB),
   interaction with calf thymus DNA   205–214

cetyl triphenyl phosphonium bromides (CTPB),
   interaction with calf thymus DNA   205–214

cGMP, see GMP

chaotropic agent                    287

Chelators        100

chemiluminescence                  358

ChiA
cloning of    340, 341–342
expression in E. coli    340, 342
ORF of      341
recombinant
   characterization of       342–343
   refolding and purification of           340–341

Chinese five-pace snake, Agkistrodon acutus,
   acutolysin A from    100–104

Chitin      339, 371

chitinase (s)   371
assay of 373, 375
bacterial 339, 342
from Serratia spp.     178, 179

Chitinase-A (ChiA)-coding gene of Pseudomonas
   sp. BK1, from Porphyra dentate, over-
   expression and characterization of        339–343

chitinolysis     179

Chitinolytic bacteria                  339

chlorocholine chloride (CCC)                  161

p-chloromercuribenzoate (PCMB), inhibitor of
   phospholipase-C                  92