|
VOLUME 43 ISSN:
0301-1208 |
NUMBER 6 |
DECEMBER 2006 CODEN: IJBBBQ
|
CONTENTS
|
Minireview |
|
|
Non-enzymatic glycation of proteins: A cause for complications in
diabetes |
337 |
|
|
|
|
|
|
|
Papers |
|
|
Overexpression of a recombinant g-glutamyltranspeptidase from Escherichia coli Novablue |
345 |
|
|
|
|
|
|
|
Mechanism of inhibition of Ca2+-transport activity of sarcoplasmic
reticulum Ca2+-ATPase by anisodamine |
351 |
|
Yuhong Pang, Xiaozhu Li, Sanbo
Qin,
Hongjie Zhang* and Jianwen Chen* |
|
|
|
|
|
3D-QSAR of histone deacetylase inhibitors as anticancer agents by
genetic function approximation |
360 |
|
Nilesh K
Wagh, Hemantkumar S Deokar,
Dhanshri C Juvale, Shivajirao S Kadam, and Vithal M Kulkarni* |
|
|
|
|
|
A new fragmentation rearrangement of the N-terminal protected amino
acids using ESI-MS/MS |
372 |
|
Zhen-Tai Zhu, Yan-Mei Li*,
Yan-Ting Guo,
Ming Sun, Yu-Fen Zhao |
|
|
|
|
|
Biosynthesis of protease from Lactobacillus
paracasei: Kinetic analysis of
fermentation parameters |
377 |
|
|
|
|
|
|
|
Facultative alkalophilic bacteria from mangrove soil with varying
buffering capacity and H+ conductance |
382 |
|
|
|
|
|
|
|
Notes |
|
|
Acute effects of a partially purified fraction from garlic on plasma
glucose and cholesterol levels in rats: Putative involvement of nitric oxide |
386 |
|
Mokni
Mehrzia, Limam Ferid, Amri Mohamed and Aouani Ezzedine* |
|
|
|
|
|
Purification of l-asparaginase
from a bacteria Erwinia carotovora and
effect of a dihydropyrimidine derivative on some of its kinetic parameters |
391 |
|
V P
Kamble, R Srinivasa Rao, Prita S Borkar, C N Khobragade* and B S Dawane |
|
|
|
|
|
395 |
|
|
|
|
|
397 |
|
|
|
|
|
399 |
|
|
|
|
|
409 |
|
|
|
|
|
413 |
|
|
|
|
——————
*Author
for correspondence
AUTHOR INDEX
|
Bhise S B |
337 |
|
Borkar P S |
391 |
|
Chen J |
351 |
|
Dawane B S |
391 |
|
Deokar H S |
360 |
|
Ezzedine A |
386 |
|
Ferid L |
386 |
|
Guo Y-T |
372 |
|
Haq I |
377 |
|
Hu H-Y |
345 |
|
Ignacimuthu S |
382 |
|
Juvale D C |
360 |
|
Kadam S S |
360 |
|
Kamble V P |
391 |
|
Kannan P |
382 |
|
Khobragade C N |
391 |
|
Kulkarni V M |
360 |
|
Li X |
351 |
|
Li Y-M |
372 |
|
Lin L-L |
345 |
|
Mehrzia M |
386 |
|
Mohamed A |
386 |
|
Mourya V K |
337 |
|
Mukhtar H |
377 |
|
Nawale R B |
337 |
|
Pang Y |
351 |
|
Paulraj M G |
382 |
|
Qin S |
351 |
|
Rao R S |
391 |
|
Sun M |
372 |
|
Wagh N K |
360 |
|
Weng Y-M |
345 |
|
Yao Y-F |
345 |
|
Zhang H |
351 |
|
Zhao Y-F |
372 |
|
Zhu Z-T |
372 |
Minireview
Indian Journal of Biochemistry & Biophysics
Vol.
43, December 2006, pp. 337-344
Non-enzymatic glycation of proteins: A cause for complications in diabetes
R B Nawale, V K Mourya# and S B Bhise*
Govt. College of Pharmacy, Osmanpura, Aurangabad 431 005, India
*Govt. College of Pharmacy, Vidyanagar, Karad, Satara 415 124, India
Received 29 May 2006; revised 20 November 2006
Diabetes mellitus is one of the most common non-communicable diseases, and is the fifth leading cause of death in most of the developed countries. It can affect nearly every organ and system in the body and may result in blindness, end stage renal disease, lower extremity amputation and increase risk of stroke, ischaemic heart diseases and peripheral vascular disease. Hyperglycemia in diabetes causes non-enzymatic glycation of free amino groups of proteins (of lysine residues) and leads to their structural and functional changes, resulting in complications of the diabetes. Glycation of proteins starts with formation of Shiff’s base, followed by intermolecular rearrangement and conversion into Amadori products. When large amounts of Amadori products are formed, they undergo cross linkage to form a heterogeneous group of protein-bound moieties, termed as advanced glycated end products (AGEs). Rate of these reactions are quite slow and only proteins with large amounts of lysine residues undergo glycation with significant amounts of AGEs. The formation of AGEs is a irreversible process, causing structural and functional changes in protein leading to various complications in diabetes like nephropathy, retinopathy, neuropathy and angiopathy. The present review discusses about role of glycation in various complications of diabetes.
Keywords: Diabetes, Glycated protein,
Advanced glycated end products, Diabetic retinopathy, Diabetic neuropathy,
Diabetic nephropathy, Diabetic angiopathy
# E-mail: vkmourya_pharmacy@yahoo.com
Papers
Indian Journal of Biochemistry & Biophysics
Vol.
43, December 2006, pp. 345-350
Overexpression of a recombinant g-glutamyltranspeptidase from
Escherichia coli Novablue
Ya-Feng Yao1, Yih-Ming Weng1, Hui-Yu Hu 2 and Long-Liu Lin3,*
1Graduate Institute of Food Science, National Chiayi University, 300 University Road, 60083 Chiayi, Taiwan
2Department of Food and Nutrition, Hungkuang University, Taichung 433, Taiwan
3Department of Applied Chemistry, National Chiayi University, 300 University Road, 60083 Chiayi, Taiwan
Received 23 May 2006; revised 03 October 2006
A truncated Escherichia coli Novablue g-glutamyltranspeptidase (EcGGT) gene, lacking the first 48-bp coding sequence for part of the signal sequence, was amplified by polymerase chain reaction (PCR) and cloned into expression vector pQE-30 to generate pQE-EcGGT. The maximum production of His6-tagged enzyme by E. coli M15 (pQE-EcGGT) was achieved with 0.1 mM IPTG induction for 12 h at 20°C. The overexpressed enzyme was purified to homogeneity by nickel-chelate chromatography to a specific transpeptidase activity of 4.25 U/mg protein and a final yield of 83%. The molecular masses of the subunits of the purified enzyme were determined to be 41 and 21 kDa respectively by SDS-PAGE, indicating the precursor EcGGT still undergoes the post-translational processing even in the truncation of signal sequence. His6-tagged EcGGT migrated relative to the molecular mass of approximately 120 kDa and its heterodimeric structure was confirmed by a native-PAGE gel.
Keywords: Escherichia coli, g-Glutamyltranspeptidase, Signal sequence, Overexpression, Nickel-chelate chromatography
*E-mail: llin@mail.ncyu.edu.tw
Indian
Journal of Biochemistry & BiophysicsVol.
43, December 2006, pp. 351-359
Mechanism of inhibition of Ca2+-transport
activity of sarcoplasmic reticulum
Ca2+-ATPase by anisodamine
Yuhong Pang, Xiaozhu Li, Sanbo Qin, Hongjie Zhang* and Jianwen Chen*
Institute of Biophysics, Academy Sinica, 15 Datun Road, Chaoyang District, Beijing 100101, China
Received 09 June 2006; revised 13 November 2006
The mechanism of inhibition of Ca2+-transport activity of rabbit sarcoplasmic reticulum Ca2+-ATPase (SERCA) by anisodamine (a drug isolated from a medicinal herb Hyoscyamus niger L) was investigated by using ANS (1-anilino-8-naphthalenesulfonate) fluorescence probe, intrinsic fluorescence quenching and Ca2+-transport activity assays. The number of ANS binding sites for apo Ca2+-ATPase was determined as 8, using a multiple-identical binding site model. Both anisodamine and Ca2+ at millimolar level enhanced the ANS binding fluorescence intensities. Only anisodamine increased the number of ANS molecules bound by SERCA from 8 to 14. The dissociation constants of ANS to the enzyme without any ligand, with 30 mM anisodamine and with 15 mM Ca2+ were found to be 53.0 mM, 85.0 mM and 50.1 mM, respectively. Both anisodamine and Ca2+ enhanced the ANS binding fluorescenc with apparent dissociation constants of 7.6 mM and 2.3 mM, respectively, at a constant concentration of the enzyme. Binding of anisodamine significantly decreased the binding capacity of Ca2+ with the dissociation constant of 9.5 mM, but binding of Ca2+ had no obvious effect on binding of anisodamine. Intrinsic fluorescence quenching and Ca2+-transport activity assays gave the dissociation constants of anisodamine to SERCA as 9.7 and 5.4 mM, respectively, which were consistent with those obtained from ANS-binding fluorescence changes during titration of SERCA with anisodamine and anisodamine + 15 mM Ca2+, respectively. The results suggest that anisodamine regulates Ca2+-transport activity of the enzyme, by stabilizing the trans-membrane domain in an expanded, inactive conformation, at least at its annular ring region.
Keywords: Anisodamine, Sarcoplasmic reticulum, Ca2+-ATPase, Ca2+-transport activity, ANS binding fluorescence, Conformational change
E.mail: hjzhang@sun5.ibp.ac.cn
Indian Journal of Biochemistry & Biophysics
Vol.
43, December 2006, pp. 360-371
3D-QSAR of histone deacetylase inhibitors as anticancer agents by genetic function approximation
Nilesh K Wagh, Hemantkumar S Deokar, Dhanshri C Juvale, Shivajirao S Kadam and Vithal M Kulkarni*
Department of Pharmaceutical Chemistry, Poona
College of Pharmacy, Bharati Vidyapeeth Deemed University,
Erandwane, Pune 411 038, India
Received 08 June 2006; revised 31 August 2006
Histone deacetylases (HDACs) play a critical role in gene transcription and are implicated in cancer therapy and other diseases. Inhibitors of HDACs induce cell differentiation and suppress cell proliferation in the tumor cells. Although many such inhibitors have been designed and synthesized, but selective inhibitors for HDAC isoforms are lacking. Various hydroxamic acid analogues have been reported as HDAC inhibitors. Here, we report a three-dimensional quantitative structure-activity relationship (3D-QSAR) study performed using genetic function approximation (GFA) for this class of molecules. QSAR models were generated using a training set of 39 molecules and the predictive ability of final model was assessed using a test set of 17 molecules. The internal consistency of the final QSAR model was 0.712 and showed good external predictivity of 0.585. The results of the present QSAR study indicated that molecular shape analysis (MSA), thermodynamic and structural descriptors are important for inhibition of HDACs.
Keywords: 3D-QSAR; Genetic function approximation, Anticancer agents, Histone deacetylases, Hydroxamic acid analogues, Physico-chemical descriptors
*E-mail: vivivips5@gmail.com
Indian Journal of Biochemistry & Biophysics
Vol.
43, December 2006, pp. 372-376
A new fragmentation rearrangement of the N-terminal protected
amino acids using ESI-MS/MS
Zhen-Tai Zhu, Yan-Mei Li*, Yan-Ting Guo, Ming Sun and Yu-Fen
Zhao
The Key Laboratory of Bioorganic Phosphorus
Chemistry & Chemical Biology (Ministry of Education),
Department of Chemistry, Tsinghua University, Beijing 100084, P. R. China
Received 23 February 2006; revised
12 November 2006
A novel
fragmentation rearrangement reaction with a carboxyl oxygen negative charge
migration was observed in the N-terminal protected amino acids including
Fmoc-protected phosphoserine, phosphothroenine, and phosphotyrosine and their
analogues using the electrospray ionization tandem mass spectrometry
(ESI-MS/MS). The possible mechanism of a five-membered ring transition state
was proposed and supported by the further experiments. It was found that the tendency
of the rearrangement was determined by the blocking status of its C-terminal
and the reaction was proved to be independent of the N-terminal and
side-chain protecting groups of the amino acids.
Keywords: Terminal-protected amino acids, ESI-MS/MS, Electronic migration, Rearrangement
*E mail: liym@mail.tsinghua.edu.cn
Indian Journal of Biochemistry & Biophysics
Vol.
43, December 2006, pp. 377-381
Biosynthesis of protease from Lactobacillus paracasei: Kinetic analysis of fermentation parameters
Ikram-ul-Haq and Hamid Mukhtar*
Institute of Industrial Biotechnology, G.C. University, Lahore 54000, Pakistan
Received 31 May 2006; revised 21 November 2006
Fifteen strains of Lactobacillus species, isolated from different samples of curd were screened for their ability to produce more extracellular protease. The proteolytic activities of these strains based on casein hydrolysis showed a variation of 1.26-5.80 U ml-1, with Lactobacillus IH8 showing the maximum activity and was identified as L. paracasei. Different cultural conditions for enhanced production of protease by L. paracasei were optimized. The optimal conditions for production of the enzyme were an incubation temperature of 35°C and a medium pH of 6.0. The maximum proteolytic activity of L. paracasei (7.28 Uml-1) was achieved after 48 h of cultivation. The kinetic parameters such as product yield (Yp/x), growth yield (Yx/s), specific product yield (qp) and specific growth yield (qs) coefficients also revealed that the values of experimental results were kinetically significant.
Keywords: Protease, Lactobacillus, Kinetics, Medium pH, Incubation temperature
*E-mail: hamidwaseer@yahoo.com
Indian Journal of Biochemistry & Biophysics
Vol.
43, December 2006, pp. 382-385
Facultative alkalophilic bacteria from mangrove soil with varying buffering capacity and H+ conductance
P Kannan, S Ignacimuthu* and M Gabriel Paulraj
Entomology Research Institute, Loyola College, Chennai 600 034, India
Received 19 May 2006; revised 20 September 2006
Facultative alkalophilic bacteria Planococcus sp. (EMGA-26), Bacillus sp. (EMGA-29) and Corynebacterium spp. (EMGA-33 and 130) were isolated from mangrove soil samples. Neutrophiles were predominant than alkalophiles. Buffering capacity and membrane H+ conductance were investigated for the strains grown in PPYG medium at pH 10.5 using acid pulse technique. Bacillus sp. showed higher buffering capacity than Planococcus sp. and Corynebacterium spp. Buffering capacity was two-fold higher in Corynebacterium sp. EMGA-33 than in EMGA-130. The membrane H+ conductance was high in Bacillus sp. and was directly proportional to the buffering capacity values. The Bacillus sp. (EMGA-29) had higher cell membrane adaptability in high pH environment than the Planococcus sp. and Corynebacterium spp.
Keywords: Facultative alkalophile, Buffering capacity, H+
conductance, Planococcus, Bacillus, Corynebacterium
*E-mail: eri_lc@hotmail.com
Notes
Indian Journal of Biochemistry & Biophysics
Vol.
43, December 2006, pp 386-390
Acute effects of a partially purified fraction from garlic on plasma
glucose and cholesterol levels in rats: Putative involvement of
nitric oxide
Mokni Mehrzia1, Limam Ferid2, Amri Mohamed1 and Aouani Ezzedine1*
1Laboratoire de Physiologie de la Nutrition, Faculté des Sciences de Tunis, Campus Universitaire El Manar II, 2092 Tunis, Tunisia
2Laboratoire Interactions Légumineuses-Microorganismes, Centre de Biotechnologie, Technopole Bordj Cédria, Tunisia
Received 03 August 2006; revised 15 November 2006
Garlic has been
extensively used as a medicinal plant. Most of its numerous beneficial effects
such as antioxidant, antibacterial, antitumoral involve sulfur-derived amino
acids. In the present work, we reevaluated the acute effects of aqueous extract
of garlic on plasma glucose and cholesterol levels in normal rats. Control
(vehicle H2O) or garlic extract-treated group at 100-120 mg
protein/kg body wt were intraperitoneally injected (IP) and glucose,
cholesterol, insulin and nitric oxide metabolites levels were determined after
a short-term duration of 6 h. We confirmed that garlic contained an active
fraction, exerting both glucose and cholesterol-lowering activity. The
glucose-lowering effect was triggered by an increase in insulinemia.
Preliminary study indicated that the active agent was different from
S-allyl-cysteine-sulfoxide, the active principle implicated in hypoglycaemic
and hypolipidemic effects of garlic or arginine. The mechanism of action seemed
to involve nitric oxide (NO), which increased time and dose-dependently. The
garlic effects were abolished by diphenyleneiodonium chloride (DPI = 1 mg/kg
body wt), a specific inhibitor of NO production, suggesting the involvement of
constitutive nitric oxide synthase.
Keywords: Garlic, Rat, Glucose, Cholesterol, Insulinemia, Nitric oxide.
*E-mail: ezzedine_aouani@yahoo.fr
Indian Journal of Biochemistry & Biophysics
Vol.
43, December 2006, pp. 391-394
Purification of l-asparaginase
from a bacteria Erwinia carotovora and
effect of a dihydropyrimidine derivative on some of its kinetic parameters
V P Kamble1, R Srinivasa Rao1, Prita S
Borkar1,
C N Khobragade1* and B S Dawane2
1School of
Life Sciences, Biotechnology Research Laboratory, Swami Ramanand Teerth
Marathwada University,
Nanded (MS) 431 606
2Department
of Chemistry, Yeshwant Mahavidyalaya,
Nanded (MS) 431 606
Received 19 August 2006; revised 17
November 2006
l-Asparaginase shows antileukemic activity and is generally administered in the body in combination with other anticancer drugs like pyrimidine derivatives. In the present study, L-asparaginase was purified from a bacteria Erwinia carotovora and the effect of a dihydropyrimidine derivative (1-amino-6-methyl-4-phenyl-2-thioxo, 1,2,3,4-tetrahydropyrimidine-5-carboxylic acid methyl ester) was studied on the kinetic parameters Km and Vmax of the enzyme using l-asparagine as substrate. The enzyme had optimum activity at pH 8.6 and temperature 35°C, both in the absence and presence of pyrimidine derivative and substrate saturation concentration at 6 mg/ml. For the enzymatic reaction in the absence and presence (1 to 3 mg/ml) of dihydropyrimidine derivative, Km values were 7.14, 5.26, 4.0, and 5.22 M, and Vmax values were 0.05, 0.035, 0.027 and 0.021 mg/ml/min, respectively. The kinetic values suggested that activity of enzyme was enhanced in the presence of dihydropyrimidine derivative.
Keywords: Erwinia carotovora, l-Asparaginase activity, Dihydropyrimidine derivative
*Email: cnkhobragade@rediffmail.com
Indian Journal of Biochemistry & Biophysics
Vol.
43, December 2006, pp. 395-396
TRendys
Meeting Report 2006
The thirteenth meeting of TRendys in Biochemistry, a
forum to discuss frontier areas and emerging concepts in biochemistry, was held
at National Institute of Nutrition (NIN), Hyderabad during August 18-19, 2006.
Dr. M Raghunath, Deputy Director, NIN, convener of the meeting, welcomed the
gathering comprising eminent scientists, research scholars and students.
Prof. Kalluri Subba Rao, National Convener, TRendys in Biochemistry briefed the
genesis of TRendys and gave the highlights of the TRendys past meetings. Prof.
T Ramasarma, who originally conceived this type of meetings, traced the growth
of the TRendys over the years and mentioned how scientists in the country are
bogged down with lots of administrative responsibilities, travel, membership in
various committees, etc. and how that is equated with the growth of the
scientist!
Padmasri Dr. Seyed E Hasnain, Vice
Chancellor, University of Hyderabad, Hyderabad, in his oration talk “Tracing Human Ancestry Using Viruses and
Other Commensals ” traced the origin and migration of human ancestors using
virus and other commensals. He outlined the problems of human origins and
migrations and the difficulties associated with such studies, and listed
various tools such as archaeological, linguistic and genetic markers to trace
human ancestry. He also briefed about the utility of mutations, micro-satellites
and haplotype analysis for individual population, forensic and archaeological
applications, based on the length of the micro-satellites. In the second part
of this talk, dealt upon the construction of phylogenetic trees, their uses and
various algorithms used for computations. Citing suitable examples, he
emphasized that viruses and commensals co-existing across the time scale can be
used conveniently to trace the human migration. In recognition of his
thought-provoking oration lecture, Dr. Hasnain was felicitated and presented
with a silver plaque by Dr. B Sesikeran the Director, NIN, the host
Institution,.
Prof. T Ramasarma (Center for DNA
Finger-printing and Diagnostics, Hyderabad), in his talk “Give an Enzyme a Name: You will not Know its True Functions” shared
some of his experiences with superoxide dismutase (SOD), an enzyme that
catalyzes dismutation of superoxide radicals (O2·-
+ O2·- + 2H+ O2 + H2O2).
Based on his experiences, he observed that SOD could catalyze the reverse
reaction leading to production of superoxide radical in the presence of
vanadate and other metal ions. He shared the difficulties encountered in
convincing the reviewers of various journals about the reverse reaction of SOD.
He emphasized, “because we already settled to a name for a given protein, which
in itself describes certain specific function, this leads to a biased approach”.
He pointed out that it is being increasingly recognized that many proteins are
multi-functional, and their function depends on the cellular demand and
conditions at the given period.
Dr. Raghu Kalluri, Harvard Medical School,
USA, spoke on “From an Experiment to a
Drug” as a part of the “Spikes and Flashes” session introduced at this
meeting. He emphasized the importance of thinking towards a clinical problem
while doing basic research. He shared that basic research is exciting and
rewarding in terms of publications, yet one should constantly focus on the
clinical utility of the work. Therefore, he urged the group to work on existing
health problems leading to development of drugs.
Dr. M N V Prasad, University of Hyderabad,
spoke (Spikes and Flashes) on “Healing
Plants that Accumulate and Hyper accumulate Toxic Trace Elements: Risk or
Remedies for Traditional Systems of Medicine”. He presented data on heavy
metal content of various plants, herbs that are commonly used as food and
medicine. He expressed his concern on the high concentrations of toxic metal
ions in many commonly used plants have, particularly when cultivated in
industrial areas. He cautioned that green leafy vegetables like spinach and
amaranth are being grown in unhygienic and polluted areas, which have high
concentrations of toxic metals, and hence pose potential health risks.
Prof. V Sitaramam, University of Pune, in his
talk on “Plant Yield: What to Measure” highlighted the lack
of early markers for measuring the yield of a plant, despite its routine use in
selecting seed varieties. He added that plant growth patterns, branching
patterns etc. are not of much use in measuring the yield. He concluded that
measuring oxygen consumption of an early seedling would correlate with its
growth and possible productivity.
Prof. J Shobhanaditya, Osmania University
Hyderabad, in his talk (Spikes and Flashes) on “Cellular Functions of Ubiquitin” explained the ubiquitin-mediated
protein degradation mechanisms. He provided a diagrammatic representation of
various proteins and enzymes involved in protein degradation, and role of
proteasomes in protein processing.
Dr. Amitabh Chattopadhyay, Centre for
Cellular and Molecular Biology, Hyderabad spoke about the “ Bloch Hypothesis and the Evolution of
Cholesterol: How Essential is Cholesterol”. He dealt upon about the weird
nature of cholesterol and its importance in metabolism and focused on
biosynthesis of cholesterol and elucidated the Bloch and Kandutsch pathways. He
also highlighted the clinical manifestations of defective cholesterol
biosynthesis (Smith-Lemlie Syndrome), where there is a increased formation of 7-dehydrocholesterol,
rather than cholesterol, due to an apparent block in 7-delta reductase. The
possible replacement of cholesterol with desmosterol in in vitro models was also discussed.
Dr. Bhanuprakash Reddy, National Institute of
Nutrition, Hyderabad speaking on “Nutrition
Research in the Era of Omics and Beyond” stressed the importance of
understanding the molecular mechanisms and network of alterations rather than
single molecules, either due to supplementation or deficiency of nutrients,
particularly micronutrients. He outlined the various frontier areas of
nutrition research being carried out at NIN, Hyderabad. He stressed that
research should continue on maternal under-nutrition and its consequences, role
of dietary factors on degenerative diseases, bio-availability screening
methods, diabetes and obesity research as these complications are directly
linked to the nutrition.
Prof. Sohan Modak (IGIB, Delhi) on his talk
on “Multiparametric Consensus Molecular
Phylogenetic Trees in 3-D” explained various ways of constructing the
phylogenetic trees, based on phenotypic and genotypic markers. Some of the
problems associated with statistical methodologies being used for constructing
phylogenetic trees were highlighted. Examples were presented to demonstrate
that same data would give different results, depending on the algorithms used.
Finally, he presented his recent work on constructing 3-D models with and
without roots. He emphasized that this kind of visualization increases the
clarity of the data and is easy to understand and interpret.
Prof. Kalluri Subba Rao, University of
Hyderabad, in his talk (Spikes and Flashes) on “Unusual Paths to Discovery: The Story of Lamin A” discussed about
‘Hutchinson-Gilford Progeria Syndrome’ (HGPS), a genetic disorder characterized
by rapid aging and death during second decade. He explained the story of an
American doctor couple, with a son afflicted with this genetic disorder, their
unprecedented struggle to wake up the scientific community of that country, and
finally succeeding in identifying that a large deletion in the lamin A gene as
possible locus. He emphasized that a special kind of scientific culture and
scientific temper are needed for achieving such successes.
Dr. K P Mohankumar, IICB, Kolkata speaking
on “The Aging Mitochondria” explained
that mitochondrial genes are not inherited by the same mechanism as nuclear
genes. At fertilization of an egg by a sperm, the egg nucleus and sperm nucleus
each contribute equally to the genetic make-up of the zygote nucleus. In
contrast, the mitochondria, and therefore the mitochondrial DNA, usually comes
from the egg only. He presented evidences to indicate that sperm's mitochondria
enters the egg, but are destroyed and do not contribute their genes to the
embryo.
M Raghunath*, B Sridhar and
P Raghu
National Institute of
Nutrition
Hyderabad 500007
*E-mail:manchalar@yahoo.com
ANNOUNCEMENT
33rd Indian
Immunology Society Conference
(28th–31st January 2007, AIIMS, New Delhi)
The Indian Immunology Society proudly announces its “33rd Indian Immunology Society Conference” on “Molecular and Clinical Immunology in Health and Disease” being organized by the Department of Biochemistry, All India Institute of Medical Sciences (AIIMS), New Delhi, during 28—31 January 2007 at Jawaharlal Nehru Auditorium, AIIMS, New Delhi. The conference coincides with the Golden Jubilee celebrations of AIIMS. The CME program on current trends in immunology, scheduled for the evening of inaugural day would provide an excellent opportunity to students to directly interact with distinguished scientists and experts in the field.
The conference would have six symposia encompassing a variety of topics viz. current concepts in immunology and approaches to immunological research, and tools and techniques used in research and clinical immunology laboratories. Invited talks include the following topics:
Congress Secretariat:
Prof. D N Rao
Organizing Secretary
Department of Biochemistry
All India Institute of Medical Sciences, Ansari Nagar
New Delhi-110029, India
Tel: 91-11-26593545 (O); 26195609 (R); Fax: 26588641, 9868592706 (M)
Email: immunocon33@rediffmail.com
Website: http://wwwaiims.ac.in; http://www.indianimmunology.org
|
Adhya M |
94 |
|
Advani
S H |
7 |
|
Ahmad
R |
217 |
|
Al-Ayed
M S |
186 |
|
Ali
I A F |
312 |
|
Angayarkanni
N |
275 |
|
Antony
B |
182 |
|
Archunan
G |
319 |
|
Banavali
S D |
7 |
|
Bandyopadhyay
S |
7 |
|
Bhatia
V S |
41 |
|
Bhise
S B |
337 |
|
Borkar
P S |
391 |
|
Chainy
G B N |
37 |
|
Chandra
A |
244 |
|
Chatterjee B P |
94 |
|
Chatterjee
Mary |
299 |
|
Chatterjee
Mitali |
7 |
|
Chatterjee
N |
233 |
|
Chen
J |
351 |
|
Chi
Z |
143,
289 |
|
Chiou S-Y |
52 |
|
Dalai
M K |
105 |
|
Das
S K |
306 |
|
Dasgupta D |
148 |
|
Datta S |
254 |
|
Dawane
B S |
391 |
|
Daxiang S |
88 |
|
Deokar
H S |
360 |
|
Dikshit
M |
69 |
|
Dixit R |
15 |
|
Dixit S |
15 |
|
Emerole
G O |
20 |
|
Ensari
Y |
123 |
|
Ezzedine
A |
386 |
|
Farombi
E O |
20 |
|
Fatima
R A |
312 |
|
Ferid
L |
386 |
|
Gakhar S |
15 |
|
Gao
L |
289 |
|
Garg A |
82 |
|
Garg
P |
98 |
|
Ghirardi
M L |
201 |
|
Ghosh P K |
25 |
|
Girigowda
K |
295 |
|
Guo
Y-T |
372 |
|
Gupta
A K |
32 |
|
Gupta S |
254 |
|
Gupta
Y K |
69 |
|
Guruprasad
K N |
41 |
|
Haq
I |
377 |
|
Hasnain
A |
217 |
|
He S |
143 |
|
Hoque
M |
167 |
|
Hu
H-Y |
345 |
|
Husain
E |
312 |
|
Ignacimuthu
S |
382 |
|
Joshi
N |
323 |
|
Joshi
P |
323 |
|
Juvale
D C |
360 |
|
Kadam
S S |
360 |
|
Kamble
V P |
391 |
|
Kannan
P |
382 |
|
Kaskhedikar
S G |
32 |
|
Katoch
S S |
160 |
|
Kaur
K |
267 |
|
Khobragade
C N |
391 |
|
Kulkarni
V M |
360 |
|
Kumar
N |
226 |
|
Kumar
S |
226 |
|
Lai G-W |
52 |
|
Lakshmi
S |
275 |
|
Leonard
J T |
105 |
|
Li
X |
351 |
|
Li
Y-M |
372 |
|
Liang
L |
289 |
|
Lin G |
52 |
|
Lin
L-L |
345 |
|
Lin L-Y |
52 |
|
Ma L |
289 |
|
Mahmood
A |
267 |
|
Mahmood
S |
267 |
|
Mandal
C |
7 |
|
Mehrzia
M |
386 |
|
Meng C X |
284 |
|
Mishra S |
25 |
|
Misra
N |
173 |
|
Mitra
C K |
137 |
|
Mohamed
A |
386 |
|
Mohanty B P |
247 |
|
Mohanty
P |
37 |
|
Moulik S P |
254 |
|
Mourya
V K |
337 |
|
Mukhtar
H |
377 |
|
Mulimani
V H |
295 |
|
Nagarajan
S |
233 |
|
Nair
C N |
7 |
|
Naseem
I |
312 |
|
Nawale
R B |
337 |
|
OmPraba
G |
154 |
|
Onyema
O O |
20 |
|
Onyeze
G O |
20 |
|
Oommen
O V |
119 |
|
Pal
S |
7 |
|
Palaniswami
M S |
182 |
|
Pang
Y |
351 |
|
Patel A |
25 |
|
Patel
S |
69 |
|
Paulraj
M G |
382 |
|
Ponmanickam
P |
319 |
|
Prasad
O |
173 |
|
Pundir
C S |
98 |
|
Qin S |
284, 351 |
|
Ramakrishnan
S |
275 |
|
Rani
K |
98 |
|
Rao
R S |
391 |
|
Rekha
T S |
137 |
|
Roy
K |
105 |
|
Sanyal S K |
254 |
|
Saxena
A K |
32 |
|
Saxena
M |
32 |
|
Selvanayagam
S |
211 |
|
Selvi
R |
275 |
|
Sharma
S |
82, 160 |
|
Sharma
U |
323 |
|
Sil
P C |
299 |
|
Singh
M P |
69 |
|
Singh
P |
167,
226 |
|
Singha B |
94 |
|
Sinha
L |
173 |
|
Soni
L K |
32 |
|
Sreejith
P |
119 |
|
Su Z-L |
284 |
|
Subudhi U |
37 |
|
Sulochana
K N |
275 |
|
Sumathi S |
148 |
|
Sun
M |
372 |
|
Sundal
S |
160 |
|
Thippeswamy
S |
295 |
|
Tolan
V |
123 |
|
Tyagi
A |
244 |
|
Ukoha
A I |
20 |
|
Vasudevan
D M |
306 |
|
Velmurugan
D |
154, 211 |
|
Wagh
N K |
360 |
|
Wakode
S R |
32 |
|
Wei W |
284 |
|
Weng
Y-M |
345 |
|
Wenhua
R |
88 |
|
Yadav
M |
48 |
|
Yadav
S |
41 |
|
Yamane
T |
211 |
|
Yang
G |
88 |
|
Yao
S |
143 |
|
Yao
Y-F |
345 |
|
YashRoy
R C |
167 |
|
Zhang
H |
351 |
|
Zhang
S |
88 |
|
Zhao
Y-F |
372 |
|
Zhou K |
88 |
|
Zhu
Z-T |
372 |
|
A |
|
|
Achatinin-H |
|
|
for
binding of 9-OAcSAa2-6GalNAc |
7–14 |
|
ACORN |
|
|
iterative,
high throughput tool in structural genomics |
211–216 |
|
Acute lymphoblastic
leukemia (ALL) |
|
|
in
childhood |
|
|
l-asparaginase for
management of |
391 |
|
9-OAcSA-specific antibody levels as index for diagnosis and
longitudinal |
7–14 |
|
b-Adrenoceptor (bAR) agonists |
|
|
clenbuterol-induced
skeletal muscle hypertrophy,
role of metabolic and physiologic
characteristics of fibres in determination
of response to |
160–166 |
|
isoproterenol,
role in attenuating muscle atrophy
under stress, study on rat |
82–87 |
|
Advanced glycated end
products (AGEs) |
337–344 |
|
Agglutinin |
|
|
FCA,
biotinylated, for recognition of bacteria |
94–97 |
|
Air-breathing organ (ABO) |
|
|
in
teleosts, myofibrillar contractility and m-ATPase
of |
217–225 |
|
Alcoholic liver disease
(ALD) |
|
|
silymarin
from Silybium marianum as |
306–311 |
|
Algae, green |
|
|
Haematococcus pluvialis, carotenoid hydroxylase gene promoter in, characterization of |
284–288 |
|
photosynthetic,
hydrogen production by |
201–210 |
|
Alkylamine glass beads |
|
|
immobilization
of 3a-HSD
and diaphorase onto, for
determination of bile acid in serum
and bile |
98–104 |
|
ALL. See Acute lymphoblastic leukemia |
|
|
Allium sativum. See Garlic |
|
|
Amino acid(s) |
|
|
extraction
and carrier-facilitated transport through
bulk liquid membrane, use of synthetic
noncyclic receptors in |
323–326 |
|
homocysteine,
in health and diseases, biochemistry
of |
275–283 |
|
N-terminal
protected, new fragmentation rearrangement
using ESI-MS/MS |
372–376 |
|
Amlodipine besylate |
|
|
CEase
inhibition (in vitro) by, kinetics
and mechanism of |
52–55 |
|
a-Amylase |
|
|
activity,
growth and plasmids amplification in Bacillus subtilis, effect of
endosulfan on |
123–126 |
|
producing
Bacillus spp. from dhal industry waste, isolation and identification
of |
295–298 |
|
Anabas testudineus |
|
|
antioxidant
enzyme activities and lipid peroxiation
in, regulatory effect of tri- iodothyronine
on |
119–122 |
|
Anisodamine |
|
|
from
Hyoscyamus niger, inhibition of Ca2+- transport activity of SERCA by, mechanism of |
351–359 |
|
Anopheles stephens |
|
|
c-type
lysozyme from, identification and characterization
of |
15–19 |
|
1-Anilino-8-naphthalenesulfonate.
See ANS fluorescence probe ANS
fluorescence probe |
|
|
to
study conformational change of SERCA |
352 |
|
Antibacterial peptide |
|
|
scolopendrin
I from venom of Scolopendra subspinipes mutilans,
induction, purification and
characterization of |
88–93 |
|
Antibodies |
|
|
against
9-OAcSA in childhood ALL, markers for initial diagnosis and
longitudinal monitoring of |
7–14 |
|
Anticancer agents |
|
|
HDAC
inhibirtors as, 3D QSAR study using GFA |
360–371 |
|
Antileukemic activity |
|
|
of l-asparaginase from Erwinia carotovora |
391–394 |
|
Antimicrobial activity |
|
|
of
crude venom from Scolopendra
subspinipes mutilans
against Gram +/- bacteria |
90 |
|
Antioxidant(s) |
|
|
C-phycocyanin
from Lyngbya, Phormidium and Spirulina spp. |
25–31 |
|
enzyme
activities in Anabas testudineus, regulatory effect of
tri-iodothyronine on |
119–122 |
|
vitamin
E |
|
|
compared
to Phyllanthus niruri aqueous extract |
299–305 |
|
effect
on MSG-induced hepatotoxicity and oxidative
stress |
20–24 |
|
Aquatic pollution |
|
|
p53-like
protein from Lamellidens corrianus as biological indicator |
247–250 |
|
l-Asparaginase |
|
|
from
Erwinia carotovora, purification,
and effect of
dihydropyrimidine derivative on some
kinetic parameters of |
391–394 |
|
Aspergillus terreus |
|
|
ligninperoxidases
from, enzymatic characteristics
of |
48–51 |
|
Astaxanthin |
|
|
biosynthesis
in Haematococcus pluvialis, role of carotenoid hydroxylase in: characterization of respective gene
promoter from |
284–288 |
|
|
|
|
B |
|
|
Bacillus spp. |
|
|
from
mangrove soil, buffering capacity and H+ conductance of |
382–385 |
|
a-amylase producing, from dhal industry waste, isolation and identification of |
295–298 |
|
Bacillus subtilis |
|
|
endosulfan
on growth, a-amylase activity and plasmids
amplification in |
123–126 |
|
Bacteria |
|
|
facultative
alkalophilic, from mangrove soil with
varying buffering capacity and H+ conductance |
382–385 |
|
Gram-positive/Gram-negative,
biotinylated FCA for
recognition of |
94–97 |
|
Bakers' yeast |
|
|
chromosome
of, FFT study of long range correlations
in |
137–142 |
|
Begomoviruses |
182 |
|
Bemisia tabaci. See Whitefly |
|
|
Benzodiazepine receptor
(BzR) |
|
|
PBR
vs. CBR binding affinity,
selectivity requirements for:
QSAR modeling of 2- phenylimidazo[1,2-a]pyridine
acetamides |
105–118 |
|
Benzodiazepines |
|
|
chlordiazepoxide
and diazepam, CEase inhibition
by, kinetics and mechanism of |
52–55 |
|
Bile acid |
|
|
in
serum and bile, determination using 3a- HSD
and diaphorase |
98–104 |
|
Bile-salt
activated lipase. See Cholesterol
esterase |
|
|
Biliary tract diseases |
|
|
silymarin
from Silybium marianum as |
306–311 |
|
Biochemical characterization |
|
|
of
selected air-breathing teleosts |
217–225 |
|
Boc-protected amino acids
(BPAAs) |
|
|
fragment
ions observed in |
373 |
|
Bone-matrix formation |
|
|
and
osteogenesis under magnetic field stimulation
in vivo: XRD, TEM and SEM investigations |
167–172 |
|
BOOK REVIEW |
|
|
"Photosystem II. The Light-Driven Water: Plastoquinone Oxidoreductase,"
2005 (Eds: Wydrzynski &
Satoh) Vol. 22, Advances in
Photosynthesis and Respiration
(AIPH), (Ser Ed: Govindjee) |
56–58 |
|
Brij-30/Brij-92. See Surfactants |
|
|
Brushite |
226 |
|
Butoxamine |
|
|
level
for reversal of isoproterenol's ameliorative
effect on work stress- induced
skeletal muscle degeneration |
82–87 |
|
|
|
|
C |
|
|
Caediolipin |
|
|
hexagonal
phase, induced by anisodamine |
351 |
|
Calcium oxalate monohydrate
(COM) crystals |
|
|
casuative
factor of urolithiasis, XRD, EDX and
SEM investigations of |
226–232 |
|
Calculus. See Urolith |
|
|
Cardiovascular disease
(CVD) |
|
|
and
homocysteine |
278 |
|
Cardiovascular drugs |
|
|
CEase
inhibition (in vitro) by, kinetics
and mechanisms of |
52–55 |
|
Carotenoid hydroxylase |
|
|
gene
promoter in Haematococcus pluvialis,
characterization of |
284–288 |
|
Cassava |
|
|
pathogenesis-related
proteins in, induced by Bemisia tabaci feeding |
182–185 |
|
Cassava mosaic disease
(CMD) |
182 |
|
Catalase (PDB-ID:1gwe) |
|
|
interative
ACORN with ARP/wARP and REFMAC
of |
211–216 |
|
Catla catla |
|
|
biochemical
properties and adaptive diversity of
skeletal muscle myofibrils and myosin of,
correlation between |
217–225 |
|
Ca2+-transport |
|
|
activity
of SERCA, inhibition by anisodamine, mechanism
of |
351–359 |
|
CEase. See Cholesterol esterase |
|
|
Cell line |
|
|
K562
erythroleukemia cells, role of nitric oxide
during erythroid differentiation in |
251–253 |
|
Centipedes |
|
|
Scolopendra subspinipes
mutilans, scolopendrin I from venom of:
induction, purification and
characterization of |
88–93 |
|
Central benzodiazepine
receptor (CBR) |
|
|
vs. PBR, binding affinity of,
selectivity requirements for:
QSAR modeling of 2- phenylimidazo[1,2-a]pyridine
acetamides |
105–118 |
|
Channa punctata |
|
|
biochemical
properties and adaptive diversity of
skeletal muscle myofibrils and myosin
of, correlation between |
217–225 |
|
Childhood |
|
|
ALL
in l-asparaginase for
management of |
391 |
|
9-OAcSA-specific antibody levels as index for diagnosis and
longitudinal |
7–14 |
|
Chitinase |
|
|
in
cassava, induced by Bemisia tabaci
feeding |
182–185 |
|
Chlordiazepoxide |
|
|
CEase
inhibition (in vitro) by, kinetics
and mechanism of |
52–55 |
|
Cholesterol |
|
|
acute
effects of partially purified fraction from garlic
on |
386–390 |
|
level
in skeletal muscles and heart under stress,
effect of isoproterenol on |
82–87 |
|
Cholesterol esterase
(CEase) |
|
|
inhibition,
in vitro, by cardiovascular drugs, kinetics and mechanisms of |
52–55 |
|
Chromatography. See also RP-HPLC |
|
|
nickel-chelate,
for purification of overexpressed
g-glutamyltranspeptidase
from E. coli |
345–350 |
|
Circular dichroism (CD) |
|
|
far
and near-UV, to study effect of denaturants
on structure and activity of 3-HBA-6-hydroxylase |
148–153 |
|
Clarias batrachus |
|
|
biochemical
properties and adaptive diversity of
skeletal muscle myofibrils and myosin
of, correlation between |
217–225 |
|
Clenbuterol |
|
|
-induced
skeletal muscle hypertrophy, role of metabolic
and physiologic characteristics
of fibres in determination of
response to |
160–166 |
|
Clostridium spp |
|
|
diaphorase
from, use in determination of bile acid
in serum and bile |
98–104 |
|
Compactin |
|
|
HMG-CoA
reductase inhibitor, use in pharmacotherapy
for hyperlipidemia |
32 |
|
Congerin II (PDB-ID:1is3) |
|
|
eel
galectin, interative ACORN with ARP/wARP
and REFMAC of |
211–216 |
|
Corynebacterium spp. |
|
|
from
mangrove soil, buffering capacity and H+ conductance of |
382–385 |
|
Crystal structures |
|
|
congerin
II and catalase |
|
|
interative
ACORN with ARP/wARP and REFMAC
of |
211–216 |
|
Cyanobacteria |
|
|
C-phycocyanin
from Lyngbya, Phormidium and Spirulina spp., antioxidant |
25–31 |
|
l-Cysteine (l-cys) |
|
|
Cyt
c(III) reduction by, kinetics and mechanism
of |
37–40 |
|
Cyt c(III). See Ferricytochrome c |
|
|
|
|
|
D |
|
|
Denaturants |
|
|
effect
on structure and activity of 3-HBA-6- hydroxylase |
148–153 |
|
Diabetes |
|
|
complications
due to non-enzymatic glycation of
proteins |
337–344 |
|
type
I, and homocysteine |
278 |
|
Diabetic |
|
|
angiopathy |
342–343 |
|
nephropathy |
341–342 |
|
neuropathy |
340–341 |
|
retinopathy |
339–340 |
|
Diaphorase |
|
|
from
Clostridium spp, use in determination
of bile acid in serum and
bile |
98–104 |
|
Diazepam |
|
|
CEase
inhibition (in vitro) by, kinetics
and mechanism of |
52–55 |
|
Dielectrics |
|
|
and
phase transition, for study of bovine albumin-liposomes
interaction |
186–189 |
|
Diethylene glycol |
|
|
and
its derivative receptors, use in extraction and
carrier-facilitated transport of amino
acids through bulk liquid membrane |
323–326 |
|
Differential display (DD) |
|
|
use
in isolation of stress responsive Psb
A gene from drought-tolerant Oryza sativa
genotype N22 |
244–246 |
|
Dioleoylphosphatidylcholine
liposomes |
|
|
hexagonal
phase, induced by anisodamine |
351 |
|
Dipalmitoylphosphatidyl
acid (DPPA) |
|
|
phase
separation by anisodamine |
351 |
|
DNA |
|
|
polymorphism,
exhibited by stress responsive Psb A gene from drought-tolerant Oryza
sativa genotype N22 |
244–246 |
|
sequence,
spectral representation, |
137 |
|
DsDNA viruses |
|
|
genome
sequences of |
137–142 |
|
Drought tolerance |
|
|
in
wheat varieties HDR 77 and HD 2009 |
233–238 |
|
Drug delivery |
|
|
plant
oil derived micro-emulsion vehicles for |
254–257 |
|
Drugs |
|
|
cardiovascular,
in vitro CEase inhibition by, kinetics and mechanisms of |
52–55 |
|
and
toxicants, relevant genes/proteins/pathways
affected by |
70 |
|
|
|
|
E |
|
|
EcGGT
gene |
|
|
overexpression
of |
345–350 |
|
Ectopia lentis |
|
|
as
clinical symptom of homocystinuria type I |
276–277 |
|
Eel galectin. See Congerin II |
|
|
Electron microscopy |
|
|
scanning
(SEM) |
|
|
and transmission (TEM), in vivo
investigation of bone-matrix
formation and osteogenesis under in vivo magnetic field stimulation |
167–172 |
|
ultrastructure
investigations of urinary calculi |
226–232 |
|
Electrospray
ionization tandem mass spectrometry
(ESI-MS/MS) |
|
|
use
in fragmentation rearrangement of N- terminal
protected amino acids |
372–376 |
|
ELISA.
See Enzyme-linked immunosorbent
assay |
|
|
Endosulfan |
|
|
effect
on growth, a-amylase activity and plasmids
amplification in Bacillus subtilis |
123–126 |
|
Energy dispersive X-ray
(EDX) spectroscopy |
|
|
for
investigations of urinary calculi in urolithiasis |
226–232 |
|
Enkephalins |
|
|
Leu5
and Met5, vibrational dynamics of morphine
in relation to |
173–181 |
|
Enzyme kinetics |
|
|
CEase
inhibition (in vitro) by
cardiovascular drugs,
kinetics and mechanisms of |
52–55 |
|
Enzyme-linked
immunosorbent assay (ELISA) |
|
|
using
biotinylated FCA and antibiotin-HRP for
study of lectin-bacteria interaction |
94–97 |
|
BSM-ELISA,
for monitoring clinical status of ALL
patients |
7–14 |
|
Enzyme markers |
|
|
of
hepatocellular injury |
21 |
|
Erwinia carotovora |
|
|
l-asparaginase from,
purification, and effect of
dihydropyrimidine derivative on kinetic parameters
of |
391–394 |
|
Erythroid differentiation |
|
|
in
K562 erythroleukemia cells, nitric oxide levels
during |
251–253 |
|
Erythroleukemia cell line |
|
|
K562,
nitric oxide levels during erythroid differentiation
in |
251–253 |
|
Escherichia coli |
|
|
recombinant
g-glutamyltranspeptidase
from overexpression of |
345–350 |
|
ESI-MS/MS.
See Electrospray ionization tandem mass spectrometry |
|
|
|
|
|
F |
|
|
Facultative alkalophilic
bacteria |
|
|
from
mangrove soil with varying buffering capacity
and H+ conductance |
382–385 |
|
Fast-Fourier Transformation
(FFT) |
|
|
study
of 1/f correlations in viral
genomes |
137–142 |
|
FCA. See Ficus cunia
agglutinin |
|
|
Ferricytochrome c [Cyt c(III)] |
|
|
reduction
by GSH and L-cysteine, kinetics and mechanism of |
37–40 |
|
FFT. See Fast-Fourier Transformation |
|
|
Ficus cunia agglutinin (FCA) |
|
|
biotinylated,
for recognition of bacteria |
94–97 |
|
Flow cytometric analysis |
|
|
detection
of cell surface 9-OAcSGs by, application in diagnosis of
childhood ALL |
7–14 |
|
Fluorescence |
|
|
ANS
binding fluorescence probe to study conformational
change of SERCA |
351–359 |
|
Fluorescence spectroscopy |
|
|
intrinsic,
to study effect of denaturants on structure
and activity of 3-HBA-6- hydroxylase |
148–153 |
|
Fmoc-protected amino acids
(FPAAs) |
|
|
fragment
ions observed in |
373 |
|
Food flavours |
|
|
MSG,
hepatotoxicity and oxidative stress, induced
by, effect of vitamin E on |
20–24 |
|
Fusarium oxysporum |
|
|
ligninperoxidases
from, enzymatic characteristics
of |
48–51 |
|
|
|
|
G |
|
|
Galectin, Eel. See Congerin II |
|
|
Gallstone |
|
|
patient
with, bile acid determination in serum and
bile using 3a-HSD and diaphorase |
98–104 |
|
Garlic |
|
|
partially
purified fraction from, acute effects on
plasma glucose and cholesterol levels
in rats: involvement of NO |
386–390 |
|
Gene expression |
|
|
recombinant
g-glutamyltranspeptidase
from E. coli,
overexpression of |
345–350 |
|
regulation
of lactase expression and mechanism of adult-type
hypolactasia, as cause of lactose
intolerance |
267–274 |
|
MAL1 in Schizosaccharomyces pombe |
143–147 |
|
Genetic function approximation (GFA) |
|
|
use
in 3D QSAR study of HDAC inhibitors |
360–371 |
|
Genomics |
|
|
and
proteomics, contribution in understanding role
of modifying factors in Parkinson's disease |
69–81 |
|
a-2m Globulin |
|
|
in
rat preputial gland, identification by MALDI-TOF
analysis |
319–322 |
|
b-1,3-Glucanase |
|
|
in
cassava, induced by Bemisia tabaci
feeding |
182–185 |
|
Glucose |
|
|
plasma
level, acute effects of garlic extract on |
386–390 |
|
g-Glutamyltranspeptidase |
|
|
recombinant,
from E. coli, overexpression of |
345–350 |
|
Glutaraldehyde coupling |
|
|
immobilization
of 3a-HSD
and diaphorase on alkylamine
glass beads through |
101 |
|
Glutathione (GSH) |
|
|
Cyt
c(III) reduction by, kinetics and mechanism
of |
37–40 |
|
Glycation |
|
|
non-enzymatic,of
proteins: cause for complications
in diabetes |
337–344 |
|
Glycol |
|
|
di/tri/tetra-ethylene,
and its derivative receptors,
use in extraction and carrier- facilitated
transport of amino acids through bulk
liquid membrane |
323–326 |
|
Green algae |
|
|
Haematococcus pluvialis, carotenoid hydroxylase gene promoter in, characterization of |
284–288 |
|
photosynthetic,
hydrogen production by |
201–210 |
|
Guanidinium hydrochloride (Gu.HCl) |
|
|
effect
on structure and activity of 3-HBA-6- hydroxylase |
148–153 |
|
|
|
|
H |
|
|
Haematococcus pluvialis |
|
|
carotenoid
hydroxylase gene promoter in, characterization
of |
284–288 |
|
H+ conductance |
|
|
and
buffering capacityof facultative alkalophilic
bacteria from mangrove soil |
382–385 |
|
HDACs. See Histone deacetylases |
|
|
HDR 77/HD 2009 |
|
|
wheat
varieties, relative binding of seed water and
seed coat membrane stability in |
233–238 |
|
Heart |
|
|
and
skeletal muscles in rats under work stress, cholesterol
and triglyceride levels in, isoproterenol's
ameliorative effect on |
82–87 |
|
Hemin |
|
|
K562
erythroleukemia cells induced by, nitric oxide
levels during erythroid differentiation
in |
251–253 |
|
Hepatocellular injury |
|
|
enzyme
markers of |
21 |
|
Hepatotoxicity |
|
|
and
oxidative stress, MSG-induced, effect of vitamin
E on |
20–24 |
|
High throughput techniques |
|
|
ACORN
with ARP/wARP and REFMAC for high
throughput structural genomics |
211–216 |
|
Histone deacetylases
(HDACs) |
|
|
hydroxamic
acid analogues as inhibitors of 3D QSAR
study using GFA |
360–371 |
|
HMG-CoA.
See Hydroxymethyl glutaryl coenzyme A |
|
|
Homocysteine (Hcy) |
|
|
and
cardiovascular disease |
278 |
|
and
diabetes type I |
278 |
|
in
health and diseases, biochemistry of |
275–283 |
|
and
Marfan syndrome |
279 |
|
molecular
mechanisms of |
|
|
oxidative stress |
279 |
|
protein homocysteinylation |
279–281 |
|
protein thiolation |
279 |
|
and
ocular complications |
278–279 |
|
and
smoking |
279 |
|
and
thrombotic diseases |
278 |
|
Homocysteinemia |
|
|
possible
treatment for |
281 |
|
Homocystinuria type I |
|
|
clinical
symptoms and manifestations |
276–277 |
|
cystathionine-b-synthase deficiency complictions |
275–283 |
|
HSD.
See Hydroxysteroid dehydrogenase |
|
|
Human
group V secretory phospholipase A2 (hVPLA2) |
|
|
QSAR
analysis of indole analogues for inhibition
of |
154–159 |
|
hVPLA2.
See Human group V secretory phospholipase A2 |
|
|
Hydrogen (H2)
production |
|
|
by
photosynthetic green algae |
201–210 |
|
Hydroxamic acid analogues |
|
|
as
inhibitors of HDACs 3D QSAR study using GFA |
360–371 |
|
Hydroxyapatite
(HAP) |
226 |
|
3-Hydroxybenzoate-6-hydroxylase |
|
|
denaturants
on structure and activity of |
148–153 |
|
Hydroxymethyl
glutaryl coenzyme A (HMG- CoA)
reductase |
|
|
inhibitors,
condensed pyridine and pyrimidine analogs
as, pharmacophoric model of |
32–36 |
|
3a-Hydroxysteroid
dehydrogenase (3a-HSD) |
|
|
from
Pseudomonas testosteronei, use in determination of bile acid in serum
|