
Gene cloning
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Bacillus velezensis RB.IBE29 was originally isolated from the rhizospheric soil of black pepper cultivated in the Central Highlands. Previous studies showed that this bacterium was a good chitinase producer, biocontrol agent, and biofertilizer.
6p
viengfa
28-10-2024
3
0
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Vibrio parahaemolyticus is one of the dangerous pathogens of aquatic animals, including fish. The outer membrane proteins play an essential role in bacterial virulence and are potential candidates for vaccine development. In this study, the virulence of four V. parahaemolyticus strains was studied, and the result was that strain. The V. parahaemolyticus N9 has the strongest virulence with an LD50 of 106.15 CFU/mL.
8p
viinuzuka
28-02-2025
6
1
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Các kỹ thuật chính dùng trong công nghệ DNA tái tổ hợp 1.1. Khái niệm 1.2. Các enzym dùng trong công nghệ DNA tái tổ hợp 1.3. Các vector nhân dòng dùng trong công nghệ DNA tái tổ hợp 1.4. Nhân dòng gen (gene cloning) 1.5. Chọn lọc, tạo dòng và sự biểu hiện của gen 2. Các kỹ thuật chính sử dụng trong phân tích DNA 2.1. Kỹ thuật chiết tách DNA và RNA 2.2. Kỹ thuật tạo ngân hàng cDNA 2.3. Phương pháp PCR 2.4. Kỹ thuật xác định trình tự DNA 2.5. Kỹ thuật RFLP (dựa vào lai DNA/DNA) 2.6....
46p
hoatuoi0939310
26-02-2013
297
81
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Bài giảng "Công nghệ di truyền - Chương 3: Simple cloning" cung cấp cho người học các kiến thức: Vector pUC, vai trò của các gene, cắt vector và DNA, nối bằng ligase được, chuyển tất cả cấu trúc vào E.coli, Operon lacZ và IPTG, chọn dòng mang DNA tái tổ hợp,... Mời các bạn cùng tham khảo nội dung chi tiết.
55p
doinhugiobay_10
12-01-2016
117
19
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Bài giảng "Simple cloning" cung cấp cho người học các kiến thức: Vector pUC, vai trò của các gene, cấu trúc của các gen, cắt vector và DNA, nối bằng ligase được, chuyển tất cả cấu trúc vào E.coli, chọn dòng mang DNA tái tổ hợp, vector nhân tạo đầu tiên, tế bào chủ, tính chất của tế bào chủ, nhân dòng sản phẩm PCR,... Mời các bạn cùng tham khảo.
55p
doinhugiobay_12
15-01-2016
59
5
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An optogenetic upgrade for the tet - OFF system fused the inhibitor to the blue light-responsive B-LID degron and optimized the performance of this construct with regard to the number of Med25VBD repeats. This approach resulted in an optogenetic upgrade of the popular Tet-OFF (TetR-VP64, tetO7-PhCMVmin) system that allows tunable, blue light-inducible gene expression in HEK-293T cells.
5p
thuyancn
01-06-2015
34
6
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The plastid transcription kinase (PTK), a component of the major RNA polymerase complex from mustard chloroplasts, has been implicated in redox-mediated regulation of plastid gene expression. A cloning strategy to define the PTK gene(s) resulted in the isolation of a full-length cDNA for a protein with overall high homology with the a subunit of cytosolic casein kinase (CK2) that contained an N-terminal extension for a putative plastid transit peptide.
9p
system191
01-06-2013
49
4
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We report here the full coding sequence of a novel mouse putative membrane-associated mucin containing three extracellular EGF-like motifs and a mucin-like domain consisting of at least 20 tandem repeats of 124–126 amino acids. Screening a cosmid and a BAC libraries allowed to isolate several genomic clones. Genomic and cDNA sequence comparisons showed that the gene consists of 25 exons and 24 introns covering a genomic region of 52 kb. The first intron is 16 kb in length and is followed by an unusually large exon ( 9.5 kb) encoding Ser/Thr-rich tandemly repeated sequences....
10p
system191
01-06-2013
49
4
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Manganese lipoxygenase was isolated to homogeneity from the take-all fungus, Gaeumannomyces graminis. The C-terminal amino acids and several internal peptides were sequenced, and the information was used to obtain a cDNA probe by RT/PCR. Screening of a genomic library of G. graminis yielded a full-length clone of the Mn-Lipoxygenase gene. cDNA analysis showed that the gene spanned 2.6 kb and contained one intron (133 bp). Northern blot analyses indicated two transcripts (2.7 and 3.1 kb). The deduced amino-acid sequence of the Mn-Lipoxygenase precursor (618 amino acids, 67.
8p
system191
01-06-2013
41
4
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We previously reported that GTS1 is involved in regulating ultradian oscillations of the glycolytic pathway induced by cyanide in cell suspensions as well as oscillations of energy metabolism in aerobic continuous cultures. Here, we screened a yeast cDNA library for proteins that bind to Gts1p using the yeast two-hybrid system and cloned multiple TDH cDNAs encoding the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH).
10p
research12
01-06-2013
42
3
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Cytochrome c is widely distributed in bacterial species, from mesophiles to thermophiles, and is one of the best-characterized redox proteins in terms of biogenesis, folding, structure, function, and evolution. Experimental molecular biology techniques (gene cloning and expression) have become applicable to cytochrome c, enabling its engineering and manipulation. Heterologous expression systems for cytochromes c in bacteria, for use in mutagenesis studies, have been established by extensive investigation of the biological process by which the functional structure is formed. ...
7p
research12
01-06-2013
36
3
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Transglutaminase (TGase) catalyses the post-translational modification of proteins by transamidation of available glutamine residues. While several TGase genes of fish and arthropods have been cloned and appear to have similar structures to those of mammals, no homologous gene has been found in lower eukaryotes. We have cloned the acellular slime mold Physarum polycephalum TGase cDNA using RT-PCR with degenerated primers, based on the partial amino acid sequence of the purified enzyme. The cDNA contained a 2565-bp ORF encoding a 855-residue polypeptide.
10p
research12
01-06-2013
50
4
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We report the cloning and functional charaterization of the full-length cDNA and gene encoding a Toxoplasma gondii DNA repair enzyme designated TgDRE. The gene is composed of three exons separated by two introns of 780 and 630 bp, and encodes a protein with a predicted molecular mass of 49.6 kDa. The native TgDRE protein, with a molecular mass of 60 kDa, is only detected in the virulent tachyzoite stage of T. gondii. However, the transcript is present in both asexual parasite stages, virulent tachyzoite and avirulent encysted bradyzoite. ...
9p
research12
01-06-2013
38
5
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Murine pregnancy-associated plasma protein-A (PAPP-A) cDNA encoding a 1545 amino-acid protein has been cloned. We have also identified and cloned cDNA that encodes a novel variant of PAPP-A, PAPP-Ai, carrying a 29-residue highly basic insert. The point of insertion corresponds to a junction between two exons in the human PAPP-A gene. The human intron flanked by these exons does not encode a homologous corresponding insert, which is unique to the mouse.
10p
research12
01-06-2013
44
6
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A gene having high sequence homology (45–49%) with the glycerol-1-phosphate dehydrogenase gene from Methanobacterium thermoautotrophicum was cloned from the aerobic hyperthermophilic archaeon Aeropyrum pernix K1 (JCM 9820). This gene expressed in Escherichia coli with the pET vector system consists of 1113 nucleotides with an ATG initiation codon and a TAG termination codon. The molecular mass of the purified enzyme was estimated to be 38 kDa by SDS/PAGE and 72.4 kDa by gel column chromatography, indicating presence as a dimer....
8p
research12
01-06-2013
33
4
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Sugar conjugation is a major pathway for the inactivation and excretion of both endogenous and exogenous compounds. We report here the molecular cloning and functional characterization of a phenol UDP-glucosyltransferase (UGT) from the silkworm, Bombyx mori, which was named BmUGT1. The complete cDNA clone is 1.6 kb, and the gene is expressed in several tissues of fifth-instar larvae, including fat body, midgut, integument, testis, silk gland and haemocytes. The predicted protein comprises 520 amino acids and has 30% overall amino-acid identity with other members of the UGT family.
7p
research12
01-06-2013
42
4
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We found a leucine aminopeptidase (LAP; EC 3.4.11.1) to be abundant in meiotic prophase tissue of a basidiomycete, Coprinus cinereus. After direct puri®cation of the amino-peptidase component from meiocytes, we cloned the gene by degenerate PCR using partial amino-acid sequences of the puri®ed enzyme and 5¢ and 3¢ RACE. It was homologous to the eukaryotic leucine aminopeptidase gene.
7p
research12
01-06-2013
52
6
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AnN-acyl-D-amino acid amidohydrolase (N-D-AAase) was identified in cell extracts of a strain, Iso1, isolated from an environment containing N-acetyl-D-methionine. The bac-terium was classified as Variovorax paradoxusby phylo-genetic analysis. The gene was cloned and sequenced. The gene consisted of a 1467-bpORF encoding a polypeptide of 488 amino acids. TheV.
11p
research12
29-04-2013
51
3
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TheatpBandatpF genes ofPropionigenium modestumwere cloned as His-tag fusion constructs and expressed in Escherichia coli.Both recombinant subunits a and b were purified via Ni 2+ chelate affinitychromatography. A func-tionallyactive Focomplex was reassembledin vitro from subunits a, band c, and incorporated into liposomes.
7p
research12
29-04-2013
32
3
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Osmoregulated periplasmic glucans (OPGs) ofRhodobacter sphaeroidesare anionic cyclic molecules that accumulate in large amounts in the periplasmic space in response to low osmolarity of the medium. Their anionic character is pro-vided by the substitution of the glucosidic backbone by succinyl residues. A wild-type strain was subject to trans-poson mutagenesis, and putative mutant clones were screened for changes in OPGs by thin layer chromatogra-phy.
12p
research12
29-04-2013
45
6
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