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1.
Br J Biomed Sci ; 65(3): 148-52, 2008.
Article in English | MEDLINE | ID: mdl-18986104

ABSTRACT

This study aims to clarify the molecular characteristics of the urease gene operon from urease-positive thermophilic campylobacters (UPTC) obtained from different sources and in various countries. Sequence heterogeneity was observed for the promoter structures at the -35-like region among the 12 isolates examined. The most probable TTG start codon was suggested for the ureB and ureH genes, and for the ureA, E, F and G genes, ATG was suggested among all the isolates examined. Overlap was detected between ureA and ureB and between ureB and ureE among all the isolates examined. UPTC is the first example of an overlap between the two structural genes ureA and ureB. When the completely sequenced open reading frames (ORFs) for ureE, ureF, ureG and ureH were identified, non-coding regions between ureE and ureF, ureF and ureG, and ureG and ureH were also demonstrated. All six start codons of the six urease genes were demonstrated to be preceded by Shine-Dalgarno sequences among all the isolates examined. The Cys-His sequence corresponding to urease active sites were aligned perfectly and fully conserved among the three UPTC isolates examined. A putative and intrinsic p-independent transcriptional terminator was identified to be identical among all the isolates examined. A partial and putative ORF of about 200 bp in length showing high sequence similarity to GTP cyclohydrolase I was observed downstream of ureH.


Subject(s)
Campylobacter lari/enzymology , Campylobacter lari/genetics , Urease/genetics , Amino Acid Sequence , Animals , Base Sequence , Humans , Molecular Sequence Data , Operon , Sequence Alignment , Terminator Regions, Genetic
2.
Br J Biomed Sci ; 65(4): 195-9, 2008.
Article in English | MEDLINE | ID: mdl-19181038

ABSTRACT

Polymerase chain reaction (PCR) amplicons (approximately 2.5 kbp) encoding a cdt gene operon and two partial and putative open reading frames (ORFs) were identified in six urease-negative (UN) Campylobacter lari isolates using a new PCR primer pair constructed in silico. Three closely spaced and putative ORFs for cdtA, cdtB and cdtC, two putative promoters and a hypothetically intrinsic p-independent transcription terminator were found in the operon. Each ORF commenced with an ATG start codon and terminated with a TGA stop codon for cdtA and cdtB and a TAA for cdtC. Interestingly, an overlap of four nucleotides was detected between cdtA and cdtB and the non-coding region of six base pairs occurring between cdtB and cdtC. The start codons for the three cdt genes were preceded by Shine-Dalgarno sequences. Although nucleotide sequence differences were identified at seven loci in the cdtA gene, six in cdtB and two in cdtC among the seven isolates (including C. lari RM2100), no polymorphic sites occurred in the putative promoters, hypothetically intrinsic transcription terminator and the three ribosome binding sites among the seven isolates. All nine amino acid residues specific for both Escherichia coli cdtB and mammalian DNase I were completely conserved in the cdtB gene locus in the 26 C. lari isolates, as well as in C. jejuni and C. coli. No PCR amplicons were generated with urease-positive thermophilic campylobacters (UPTC; n=10) using the primer pair.


Subject(s)
Bacterial Toxins/genetics , Campylobacter lari/genetics , Escherichia coli Proteins/genetics , Amino Acid Sequence , Animals , Bacterial Toxins/classification , Campylobacter lari/isolation & purification , Charadriiformes , Cloning, Molecular , Humans , Open Reading Frames , Operon/genetics , Polymerase Chain Reaction/methods , Polymorphism, Genetic , Sequence Alignment , Sequence Analysis/methods
3.
J Appl Microbiol ; 103(1): 252-60, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17584472

ABSTRACT

AIMS: To clone, sequence and characterize the genetic organization of urease genes within urease-positive thermophilic Campylobacter (UPTC). METHODS AND RESULTS: An approx. 5.1-kbp region encoding a urease gene operon was identified, when recombinant plasmid DNAs from a genomic DNA library of a Japanese isolate (CF89-12) of UPTC were analysed. CONCLUSIONS: Six closely spaced and putative open reading frames (ORFs) for ureA, ureB, ureE, ureF, ureG and ureH were detected. ATG codons initiated each ORF of the UPTC urease operon except for ureB and ureH, which commenced with the most probable TTG codon. Overlaps were detected between ureA and ureB and also between ureB and ureE. Probable ribosome-binding sites and a putative rho-independent transcriptional termination region were identified. Two putative promoter structures, consisting of consensus sequences at the -35 like and -10 regions were also identified. SIGNIFICANCE AND IMPACT OF THE STUDY: Construction of a neighbour-joining tree based on the nucleotide sequence data of urease genes indicated that UPTC formed a cluster with some Helicobacter organisms separate from the other urease-producing bacteria, suggesting a commonly shared ancestry between UPTC and Helicobacter urease genes.


Subject(s)
Campylobacter/genetics , Urease/genetics , Amino Acid Sequence , Base Sequence , Campylobacter/enzymology , Cloning, Molecular , DNA, Bacterial/genetics , Gene Library , Genes, Bacterial , Helicobacter/enzymology , Helicobacter/genetics , Molecular Sequence Data , Open Reading Frames , Phylogeny
5.
Parasitol Int ; 50(4): 273-8, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11719114

ABSTRACT

Using N2 cavitation, we established a protocol to prepare the active mitochondria from Plasmodium falciparum showing a higher succinate dehydrogenase activity than previously reported and a dihydroorotate-dependent respiration. The fact that fumarate partially inhibited the dihydroorotate dependent respiration suggests that complex II (succinate-ubiquinone reductase/quinol-fumarate reductase) in the erythrocytic stage cells of P. falciparum functions as a quinol-fumarate reductase.


Subject(s)
Mitochondria/metabolism , Orotic Acid/analogs & derivatives , Orotic Acid/metabolism , Plasmodium falciparum/metabolism , Succinate Dehydrogenase/metabolism , Animals , Blotting, Western , Fumarates/metabolism , Mitochondria/enzymology , Oxygen/metabolism , Oxygen Consumption , Plasmodium falciparum/enzymology , Succinate Dehydrogenase/analysis
6.
Seishin Shinkeigaku Zasshi ; 102(5): 459-80, 2000.
Article in Japanese | MEDLINE | ID: mdl-10897678

ABSTRACT

UNLABELLED: We conducted surveys to study the magnitude and nature of psychological consequences of school children affected by the Great Hanshin Awaji Earthquake, which occurred in Kobe on January 17th, 1995. It measured 7.2 in magnitude, killed more than 6000 people and destroyed at least 170,000 buildings and houses. The investigations were carried out 4 months following of the disaster. SUBJECTS: About 9000 school children in the 3rd grade, the 5th grade, the 8th grade living in the disaster areas. About 2000 children living in distant areas were also surveyed as control subjects. METHOD: The questionnaire was in a self-descriptive format and consisted of 10 items regarding situation and behavior when the earthquake occurred and 22 items about mental health condition. The responses were rated from 1 to 4 depending on the frequency of the symptoms, and statistically analyzed. RESULT: By factor analysis, three factors were elicited. Factor 1 was interpreted as being related to fear and anxiety, factor 2 as related to depression and physical symptoms, and factor 3 as related to pro-social tendencies. The highest mean score of factor 1 was associated with the most heavily damaged areas. Less severe damage was associated with a lower mean score, and the control areas showed the lowest score. These results show that the children in the damaged areas were strongly affected. Factor 2 shows a different pattern from factor 1. The score of heavily damaged areas is conspicuously high. However, the differences between the other areas were not significant, the control areas had scores almost the same as these of the slightly damaged areas. These results may mean that in less damaged areas than in more heavily damaged areas, there was a more remarkable "heroic phase" after the disaster, which hid depressive moods and lasted longer than in the more severely damaged areas, where people had to face stern reality in the early stages. Factor 3 shows the reverse pattern of factor 2. The slightly damaged areas had the highest score. This result also shows the influence of the "heroic stage". As for the mean scores of factors 1 and 2, younger children showed higher scores. There were no differences in the scores of factor 3 between students in the 3rd grade and 5th grade. The score of the students in the 8th grade was the lowest among all. It can be seen that adolescents generally lessen their consideration for society as a developmental stage in their growth. All of the mean scores of factors 1, 2 and 3 of females are higher than those of males. In the heavily damaged areas, factor 1 is associated with an experience of being rescued and injuries of the children themselves. Factor 2 is associated with injuries of the children themselves. In the moderately damaged areas, factors 1 and 2 are associated with injuries of the children themselves and taking in victims in the children's homes. In the slightly damaged areas, factor 1 is associated with injuries within families. Factor 2 is associated with injuries within families and taking in victims in the childrens' homes. CONCLUSIONS: School-aged children exposed to a high-magnitude natural disaster had 3 categories of emotions: "fear and anxiety," "depressive mood and physical symptoms" and "pro-social tendency." The severity of disaster, younger age, and female gender were high risk factors for distress. In the heavily damaged areas, an experience of being rescued and injuries of the children themselves had a great influence on the mental health of children. In lesser damaged areas, taking in victims in the childrens' homes and injuries within families had an influence.


Subject(s)
Disasters , Mental Health , Psychology, Adolescent , Psychology, Child , Stress Disorders, Post-Traumatic/epidemiology , Adolescent , Age Factors , Child , Female , Humans , Japan/epidemiology , Male , Risk Factors , Schools , Sex Factors , Stress Disorders, Post-Traumatic/psychology , Surveys and Questionnaires
7.
Mol Biochem Parasitol ; 106(1): 63-76, 2000 Feb 25.
Article in English | MEDLINE | ID: mdl-10743611

ABSTRACT

Complex II of adult Ascaris suum muscle exhibits high fumarate reductase (FRD) activity and plays a key role in anaerobic electron-transport during adaptation to their microaerobic habitat. In contrast, larval (L2) complex II shows a much lower FRD activity than the adult enzyme, and functions as succinate dehydrogenase (SDH) in aerobic respiration. We have reported the stage-specific isoforms of complex II in A. suum mitochondria, and showed that at least the flavoprotein subunit (Fp) and the small subunit of cytochrome b (cybS) of the larval complex II differ from those of adult. In the present study, complete cDNAs for the iron-sulfur subunit (Ip) of complex II, which with Fp forms the catalytic portion of complex II, have been cloned and sequenced from anaerobic adult A. suum, and the free-living nematode, Caenorhabditis elegans. The amino acid sequences of the Ip subunits of these two nematodes are similar, particularly around the three cysteine-rich regions that are thought to comprise the iron-sulfur clusters of the enzyme. The Ip from A. suum larvae was also characterized because Northern hybridization showed that the adult Ip is also expressed in L2. The Ip of larval complex II was recognized by the antibody against adult Ip, and was indistinguishable from the adult Ip by peptide mapping. The N-terminal 42 amino acid sequence of Ip in the larval complex II purified by DEAE-cellulofine column chromatography was identical to that of the mature form of the adult Ip. Furthermore, the amino acid composition of larval Ip determined by micro-analysis on a PVDF membrane is almost the same as that of adult Ip. These results, together with the fact, that homology probing by RT-PCR, using degenerated primers, failed to find a larval-specific Ip, suggest that the two different stage-specific forms of the A. suum complex II share a common Ip subunit, even though the adult enzyme functions as a FRD, while larval enzyme acts as an SDH.


Subject(s)
Ascaris suum/genetics , Iron-Sulfur Proteins/chemistry , Multienzyme Complexes/chemistry , Oxidoreductases/chemistry , Succinate Dehydrogenase/chemistry , Amino Acid Sequence , Animals , Ascaris suum/enzymology , Base Sequence , Blotting, Northern , Blotting, Western , Caenorhabditis elegans/genetics , Chromatography, Ion Exchange , Cloning, Molecular , DNA, Complementary/chemistry , DNA, Complementary/genetics , Electron Transport Complex II , Isoenzymes/chemistry , Larva , Molecular Sequence Data , Multienzyme Complexes/metabolism , Oxidoreductases/metabolism , RNA, Helminth/analysis , Sequence Alignment , Sequence Homology, Amino Acid , Succinate Dehydrogenase/metabolism
8.
Arch Biochem Biophys ; 371(2): 284-9, 1999 Nov 15.
Article in English | MEDLINE | ID: mdl-10545216

ABSTRACT

The respiratory chain of Caenorhabditis elegans was characterized in mitochondria isolated from aerobically grown nematodes. Nematode mitochondria contain ubiquinone-9 as a major component and rhodoquinone-9 as a minor component. The ratio of ubiquinone-9/rhodoquinone-9 is higher in C. elegans mitochondria than in mitochondria from second-stage larvae of Ascaris suum, the free-living stage of porcine gut-dwelling nematode. The individual oxidoreductase activities comprising succinate oxidase and the amount of substrate-reducible cytochromes are comparable to those of mitochondria from second-stage larvae of A. suum. The specific activity of fumarate reductase is lower in C. elegans mitochondria than in mitochondria from second-stage larvae of A. suum, but still higher than in mammalian mitochondria. These results indicate that the free-living nematode C. elegans is capable of synthesizing rhodoquinone, as distinguished from aerobic mammalian species, although its mitochondria appear more aerobic than A. suum larval mitochondria.


Subject(s)
Caenorhabditis elegans/physiology , Mitochondria/metabolism , Succinate Dehydrogenase/metabolism , Ubiquinone/analogs & derivatives , Aerobiosis , Animals , Electron Transport , Spectrophotometry , Ubiquinone/metabolism
9.
Article in English | MEDLINE | ID: mdl-10622429

ABSTRACT

Trypanosome alternative oxidase (TAO) is the terminal oxidase of the respiratory chain of long slender bloodstream forms (LS forms) of African trypanosoma, which causes sleeping sickness in human and nagana in cattle. TAO is a cytochrome-independent, cyanide-insensitive quinol oxidase and these properties are quite different from those of the bacterial quinol oxidase which belongs to the heme-copper terminal oxidase superfamily. Only little information concerning the molecular structure and enzymatic features of TAO have been available, whereas the bacterial enzyme has been well characterized. In this study, a cDNA encoding TAO from Trypanosoma brucei brucei was cloned into the expression vector pET15b (pTAO) and recombinant TAO was expressed in Escherichia coli. The growth of the transformant carrying pTAO was cyanide-resistant. A peptide with a molecular mass of 37 kDa was found in the cytoplasmic membrane of E. coli, and was recognized by antibodies against plant-type alternative oxidases from Sauromatum guttatum and Hansenula anomala. Both the ubiquinol oxidase and succinate oxidase activities found in the membrane of the transformant were insensitive to cyanide, while those of the control strain, which contained vector alone, were inhibited. This cyanide-insensitive growth of the E. coli carrying pTAO was inhibited by the addition of ascofuranone, a potent and specific inhibitor of TAO ubiquinol oxidase. The ubiquinol oxidase activity of the membrane from the transformant was sensitive to ascofuranone. These results clearly show the functional expression of TAO in E. coli and indicate that ubiquinol-8 in the E. coli membrane is able to serve as an electron donor to the recombinant enzyme and confer cyanide-resistant and ascofuranone-sensitive growth to E. coli. This system will facilitate the biochemical characterization of the novel terminal oxidase, TAO, and the understanding on the mechanism of the trypanocidal effect of ascofuranone.


Subject(s)
Cytoplasm/enzymology , Escherichia coli/enzymology , Oxidoreductases/metabolism , Sesquiterpenes/pharmacology , Trypanosoma brucei brucei/enzymology , Animals , Base Sequence , Cattle , Cell Membrane/enzymology , DNA Primers , Humans , Mitochondrial Proteins , Plant Proteins , Recombinant Proteins/metabolism
10.
Jpn J Clin Oncol ; 28(2): 134-41, 1998 Feb.
Article in English | MEDLINE | ID: mdl-9544830

ABSTRACT

The main purpose of the study was to evaluate quality of life (QOL) among cancer patients using the WHOQOL-100 instrument and to see if any significant differences were seen in cancer stages, treatment status and prognosis. This study consisted of two parts; qualitative and quantitative. For the qualitative study, two focus groups were conducted by medical professionals to establish the applicability of the WHOQOL instrument in evaluating the QOL of cancer patients, but most participants were negative about using a generic instrument such as WHOQOL. For the quantitative study, 197 cancer patients (average age 55.86) from eight medical centers using the WHOQOL instrument, in addition to each patient's information sheet filled in by their own physicians, were analyzed. The average overall QOL score was 3.39. There was high reliability (Cronbach's alpha = 0.9685) and a high correlation between the psychological and the environmental domains (r = 0.7021), the physical domain and the level of independence (r = 0.6031) and social relations and the environment (r = 0.6856) and between health conditions perceived by patients and QOL scores. In addition, differences by gender, treatments and cancer sites were also found to be significantly different at the 5% significance level. The results indicated that the WHOQOL core instrument was sensitive enough to evaluate the QOL of cancer patients.


Subject(s)
Focus Groups , Neoplasms/psychology , Psychometrics/methods , Quality of Life , Adult , Aged , Female , Humans , Male , Middle Aged , Self-Assessment , Surveys and Questionnaires , World Health Organization
11.
Arch Intern Med ; 158(3): 274-8, 1998 Feb 09.
Article in English | MEDLINE | ID: mdl-9472208

ABSTRACT

OBJECTIVE: To examine the effects of the Kobe, Japan, earthquake, a life-threatening event, on stress and glycemic control in diabetic patients. PATIENTS AND METHODS: Hemoglobin A1c levels before and after the earthquake were evaluated in diabetic patients in Kobe (N = 157; magnitude, 7.2) and in Osaka, Japan, as a control (N = 277; magnitude, 4.2), where little damage to houses and traffic facilities occurred. Glycosylated hemoglobin levels were also compared with those of 2 years before and 1 year after the earthquake. The General Health Questionnaire (GHQ) and a self-administered questionnaire regarding damage to houses and relatives killed or injured were used to assess psychological and mental stresses on earthquake survivors. RESULTS: Glycemic control was aggravated in diabetic patients after the earthquake in Kobe but not in Osaka. THe GHQ scores were significantly higher in the patients in Kobe than those in Osaka. Increased hemoglobin A1c concentrations and high scores on the GHQ were especially evident in diabetic patients with severe damage to houses and/or with relatives killed or injured. CONCLUSION: These results suggest an association between chronic, life-threatening stress and the worsening of metabolic control in patients with diabetes mellitus.


Subject(s)
Blood Glucose/metabolism , Diabetes Mellitus/blood , Diabetes Mellitus/psychology , Disasters , Stress, Psychological , Adult , Aged , Female , Glycated Hemoglobin/metabolism , Humans , Japan , Male , Middle Aged , Surveys and Questionnaires
12.
Int J Parasitol ; 27(6): 617-30, 1997 Jun.
Article in English | MEDLINE | ID: mdl-9229245

ABSTRACT

Parasitic helminths exhibit greater diversity in energy metabolism than do the host animals and many have exploited unique respiratory chains as adaptations to their natural habitats. Cytochromes are involved, not only in intracellular aerobic respiration found in free-living stages, but also in the reduction of relatively oxidized compounds such as fumarate during the adult stages of parasitic helminths. In addition, most helminths retain a significant capacity to produce energy via aerobic pathways and have a mammalian type respiratory chain in their mitochondria during their development in the host. In this review, we focus on recent advances in the study of cytochromes in the respiratory chain of parasitic helminths. These include the identification of unique features of anaerobic respiration in adult parasites, the elucidation of molecular structures of the components involved and an understanding of the developmental changes that occur during the life-cycle of these parasites.


Subject(s)
Cytochromes/metabolism , Helminths/metabolism , Mitochondria/metabolism , Amino Acid Sequence , Animals , Ascaris suum/growth & development , Ascaris suum/metabolism , Caenorhabditis elegans/metabolism , Cytochrome b Group/genetics , Cytochrome b Group/metabolism , Electron Transport , Electron Transport Complex IV/genetics , Electron Transport Complex IV/metabolism , Humans , Molecular Sequence Data , Sequence Alignment
17.
Biochim Biophys Acta ; 1350(2): 119-22, 1997 Feb 07.
Article in English | MEDLINE | ID: mdl-9048878

ABSTRACT

Mitochondrial tRNA(Arg) from a nematode, Ascaris suum, was purified and sequenced at the RNA level. An unmodified adenosine was found to exist at the anticodon first position, suggesting that, contrary to the conventional wobble rule, the anticodon ACG of the tRNA can translate all the CGN codons.


Subject(s)
Anticodon/genetics , Ascaris suum/genetics , RNA, Helminth/genetics , RNA, Transfer, Arg/genetics , RNA/genetics , Animals , Base Sequence , Molecular Sequence Data , Nucleic Acid Conformation , Protein Biosynthesis , RNA/chemistry , RNA, Helminth/chemistry , RNA, Mitochondrial , RNA, Transfer, Arg/chemistry
18.
Biochim Biophys Acta ; 1276(1): 1-5, 1996 Aug 07.
Article in English | MEDLINE | ID: mdl-8764887

ABSTRACT

Complex II in the mitochondria of the adult parasitic nematode, Ascaris suum, exhibits high fumarate reductase activity in addition to succinate dehydrogenase activity and plays a key role in the anaerobic energy metabolism of the worm. In this study, the amino acid sequence of the small subunit of cytochrome b558 (cybS) in adult complex II was deduced from the cDNA isolated by immunoscreening an A. suum muscle cDNA library. Histidine residues, which are possible heme axial ligands in cytochrome b558, were found in the second transmembrane segment of the subunit. This is the first report of the primary structure of the small subunit in the two-subunit cytochrome b in mitochondrial complex II from a multicellular eukaryote.


Subject(s)
Ascaris/genetics , Cytochrome b Group/genetics , NADPH Oxidases , Succinate Dehydrogenase/genetics , Amino Acid Sequence , Animals , Ascaris/chemistry , Base Sequence , Biophysical Phenomena , Biophysics , Cloning, Molecular , Cytochrome b Group/chemistry , DNA, Complementary/genetics , DNA, Helminth/genetics , Mitochondria/chemistry , Mitochondria/enzymology , Molecular Sequence Data , Sequence Homology, Amino Acid , Succinate Dehydrogenase/chemistry
19.
Mol Biochem Parasitol ; 79(1): 61-70, 1996 Jul.
Article in English | MEDLINE | ID: mdl-8844672

ABSTRACT

Mitochondrial cytochrome c was isolated at high purity from adult Ascaris suum muscle and its molecular properties were investigated. The molecular weight of A. suum cytochrome c was determined to be 13,119 by electrospray ionization mass spectrometry. The oxidation-reduction potential of nematode cytochrome c was measured to be +248 mV; this value is comparable to those for cytochrome c from mammalian sources. The A. suum cytochrome c, like bovine heart cytochrome c, showed biphasic kinetics against bovine heart cytochrome c oxidase. Comparative kinetic studies revealed species-specificity in the reaction between cytochrome c and cytochrome c oxidase from A. suum and bovine sources. The cytochrome c content in mitochondria was highest at the second larval stage, in which the respiratory chain is the most aerobic among various developmental stages of A. suum. These data clearly show that adult A. suum cytochrome c, as isolated, is a bona fide substrate for cytochrome c oxidase in the aerobic respiratory chain of second-stage larvae.


Subject(s)
Ascaris suum/chemistry , Cytochrome c Group/chemistry , Helminth Proteins/chemistry , Muscles/chemistry , Age Factors , Amino Acid Sequence , Animals , Cattle , Cross Reactions , Cytochrome c Group/immunology , Cytochrome c Group/metabolism , Cytochromes c1 , Cytochromes c2 , Electron Transport Complex IV/metabolism , Helminth Proteins/immunology , Helminth Proteins/metabolism , Mass Spectrometry , Molecular Sequence Data , Oxygen Consumption , Potentiometry , Sequence Analysis , Spectrophotometry
20.
Arch Biochem Biophys ; 328(1): 165-72, 1996 Apr 01.
Article in English | MEDLINE | ID: mdl-8638926

ABSTRACT

A b5-type cytochrome was extracted from Ascaris suum muscle at pH 4.5 with 0.3% aluminum sulfate and purified by ammonium sulfate fractionation, ion-exchange chromatography on CM-500 Cellulofine, and gel filtration on Sephadex G-75. The hemoprotein displayed a typical absorption spectrum of cytochrome b with a midpoint redox potential of 78 mV. The N-terminal amino acid sequence was determined and revealed the N-terminus to be highly homologous to the heme-binding domain of vertebrate cytochrome b5. Using an oligonucleotide probe synthesized based on the amino acid sequence of the purified protein, the cDNA clone encoding A. suum cytochrome b5 was isolated from the lambda ZAP II cDNA library. The entire nucleotide sequence of 563 bases comprised an open reading frame of 339 bases encoding a precursor protein of 112 amino acid residues. The purified cytochrome B5 was predicted to contain 82 amino acids with a molecular mass of 9141 Da, matching the 9140 Da obtained from electrospray ionization mass spectometry, and to lack of membrane-anchor domain at the C-terminus. In contrast, an N-terminal extension of 30 amino acids, characteristic of signal peptides, was apparent. Immunoblots revealed the presence of an A. suum cytochrome b5 of 82 amino acids, but no protein with an N-terminal extension. These results demonstrate a novel cytochrome b5 possessing a presequence.


Subject(s)
Ascaris suum/chemistry , Cytochromes b5/chemistry , Muscles/chemistry , Amino Acid Sequence , Animals , Base Sequence , Cytochromes b5/genetics , DNA, Complementary/genetics , Female , Gene Library , Genetic Variation , Mass Spectrometry , Molecular Sequence Data , Potentiometry , Sequence Analysis , Sequence Homology, Amino Acid , Species Specificity , Spectrophotometry
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