Sanger institute was funded in order ...

Sanger Institute is a program of measures to pneumococcus, including the reference genomes, comparative genomics, deep within the sequence of lines and capsule biosynthesis loci sequences. Draft sequencing loci Hz. Genome representative S. pneumonia

Other genomes Help: INV104B (ST 227, serotype 1), INV200 (ST 9 14 serotypes), OXC141 (ST 180, serotype 3), A45 (serotype 3) Comparative genomics

in ST180 (strains 03_4156, 03_4183, 07_2838, 99_4038, 99_4039, 02_1198). Comparative genomics of serotype 1 (strain P1041, INV104B, 03_2672, 03_3038, 06_1370, NCTC7465)

Deep within the sequence of S. pneumonia

repeat sequence analysis, annotation software can be downloaded collaborators Brian Spratt, Imperial College, UK

Tim Mitchell, University of Glasgow, UK

Peter, Andrew, University of Leicester, UK

Kate Kluhman, Emory University, USA

Anne background Gottburg, NICD, South Africa

Leslie MakHi, CDC, USA

Kwan Soo Ko, ARFID, South Korea

Steve Baker, OUCRU, Vietnam

Lotte Lamberts, SSI, Denmark

Mark van der Linden, NRCS, Germany

Bruno Pyshon, HPA, UK

Bill Hanage, Imperial College, UK

Margaret Kaltoft, Streptococcus Group, Institute of serum, Denmark

Financing >> << S. pneumonia type 23F (Spanish 23F-1), multiple antibiotic-resistant pandemic strain. Genome size is 2221315

bp sequence and in collaboration with in collaboration with Professor Tim Mitchell of Infection and Immunity, Institute of Biomedical and Natural Sciences, University of Glasgow and Professor. Peter William Andrew Department of Microbiology and Immunology, Univesity of Leicester. Fully annotated genomes available in EMBL / GenBank database with the inventory number. Sanger Institute was funded in the sequence of each 90-capsule polysaccharide (CPS) biosynthetic clusters of S. pneumonia

in collaboration with Professor Brian Spratt Department of Epidemiology of Infectious Diseases,,, London and Dr. Margaret Kaltoft Group Streptococcus, sera Institute, Denmark. Knowledge of the complete sequence of the capsule should be important to monitor and study vaccines. Each cluster Hz increases long-PCR using primers flanking dexB on conservative and the other as described, and PCR product vyvirenoyi shotgun technique. Sizes range from 13 844 to 30 298 base pairs. All 90 sequences finished, and annotated. The sequences are available for searching on our. Sequence and preliminary annotations available for download from strattera online our. Genomes of strains INV104B (ST 227, serotype 1), INV200 (ST 9 serotypes 14) and OXC141 (ST 180, serotype 3), finished or nearly finished. The latter sequences are available for searching on our

or download our. Shotgun and data collection of these projects are also available from our. .

Streptococcus pneumonia 2.

Includes cough, fever and chest pain when breathing in. Pneumonia symptoms can be tolerated in early disease. What causes people to seek medical intervention is the aggravation of symptoms. Indeed, people generally tend to control certain diseases in the home or even have it checked for proper medical intervention. The general opinion that hospitalization is costly and, while symptoms persist, patients strattera without prescritpion, people prefer to stay at home than in hospital. However, pneumonia can be fatal if untreated. So good to know that pneumonia is to recognize the right time to see a doctor for suspected pneumonia case before it is too late. Pneumonia is a common lung infection that can affect one or both lungs. The main causes are bacteria, viruses and fungi. In pneumonia, bacteria will attack the air sacs and mucosa of the respiratory tract. Thus, the body will try to resist, these microorganisms through the inflammatory process. Finally, the person will show symptoms associated with the presence of infection. Method of transmission of the disease is in the air drops. This means that a person can get the disease from inhaling bacteria that cause pneumonia or suspended in the air drops or discharge from an infected person. These bacteria spread through the air by an infected person by sneezing or coughing. Moreover, a person may be the risk of pneumonia in the presence of other factors that affect the ability of cough with secretions from the mouth and nasal cavity to avoid them getting into the lungs and cause infection. Some of these conditions, stroke, neurological degenerative disease and problems with swallowing. Aging may risk a person gets pneumonia. In addition to causing body functions such as swallowing, older people was weakened immune system. In addition, when the immune system does not work, the body less able to resist disease acquisition. Pneumonia symptoms can begin with symptoms of cold and as it progresses, more forms will happen that will distinguish pneumonia from other illnesses. General >> << Pneumonia symptoms 1. Sneezing

2. Sore throat

3. High

4. Productive cough (sputum rusty color)

5. Chills

6. Chest pain

7. Difficulty breathing

8. Cyanosis of pneumonia severity of symptoms depend on what part of the lung affected by the infection. The infection, which likely affects the airways in the lungs will vary due to increase in sputum coughed from time. On the other hand, when air bags are affected structures, signs are more associated with abnormal gas exchange. The blood becomes less oxygen due to the presence of fluid and pus in the air sacs, leading to difficulty breathing and

cyanosis (bluish color which can be seen on the skin, nail and lip). Fever, chills and pain in the chest associated with the presence of inflammation. However, some people are easier to display

Pneumonia symptoms such as a light headache, muscle pain and progressive cough. X-ray of the chest is the radiological examination, which confirms the presence of pneumonia. Is it displays the proportion of light effect. Sputum is used to determine which organism caused the disease. In fact, there are certain organisms that serve as the causative agent of pneumonia. In other words, not all pulmonary infections are pneumonia. As mentioned earlier, pneumonia can be caused by bacteria, viruses and fungi. Below is a specific list of the most common causative agents of pneumonia:

1. Streptococcus pneumonia 2. Klebsiella pneumonia 3. Hemophilus influenza 4. Mycoplasma pneumonia 5. Legionella pneumonia 6. Chlamydia pneumonia virus 1. Adenoviruses 2. Rynovirusy 3. Influenza viruses 4. Respiratory syncytial virus 5. Parainfluenza virus Mushrooms 1. Histoplasmosis 2. Coccidiomycosis 3. Blastomycosis 4. Aspergillosis 5. Cryptococcosis addition, pneumonia can be diagnosed, as well as through a blood test and bronchoscopy. Blood tests are usually conducted to determine whether a significant increase in individual components Leukocytes (WBC), such as neutrophils and lymphocytes. These components are somehow differentiate or Pneumonia is a bacterial origin or may be caused by other microorganisms. Increased neutrophil mean bacterial infection, while increasing lymphocyte mean other agents involved. Bronchoscopy performed using the bronchoscope. This thin tube that is flexible enough to pass through the mouth or nose to have a direct view of the airways. It can also be used for obtaining samples of tissue or secretions from infected parts of the lungs. For treatment of pneumonia is based on the pathogen. Pneumonia caused by bacteria and fungi treated with specific antibiotics. Some of the most common antibiotics used to treat pneumonia is penicillin, combined amoksillin and clavulanic acid (Augmentin), azithromycin, levofloxacin and fluconazole. On the hand, viral pneumonia as a restriction or he decides on its own and depends on the immune system. Thus, the best way to handle this type of pneumonia is to boost the immune system by taking enough rest and nutrition. must be present, respectively. Pneumonia is very common as the disease and increase its popularity as it becomes one of the most common causes of death of thousands of people worldwide. Other respiratory diseases, symptoms and diagnosis >>. <<

It was the first time

Amazing natural alternative to antibiotics.

There is no disease-causing bacteria that can live in the presence of

even the slightest traces of metallic silver. The Best Colloidal Silver >> << contains only natural ingredients that help the body fight infections

as synthetic antibiotics, but without the damaging effects >> << parties. Its natural deep golden color characteristic of high quality >>. Concentration << twenty parts per million of silver contained

is very effective, safe design. Higher concentrations may

actually be less effective because they can interfere with beneficial strattera 40mg bacteria

discoloration of the skin and cause, even if for internal use. Each family >> << wanting the best natural health should have a bottle of Colloidal Silver >> << in the medicine cabinet. "Let me tell you that

when our kids were chicken pox, a few years ago, we spray her with

colloidal silver from head to toe, and most surprising was that the children

. no more itchy chicken pox ran its turn, but when

everything was over, there were no traces of ash yet we were very happy

those results. ". - SM "My daughter was >> << sore throat and fever 102ye. I spray her throat colloidal silver. Within 48 hours of sore throat and fever had disappeared. It was the first time

it never to return so quickly and without taking antibiotics

".

KB Silver in colloidal form

been proved useful against various infections and

non-toxic in reasonable concentrations of all species of fungi,

bacteria, protozoa, parasites and some viruses. Higher grade colloidal

SILVER conducted a technical electrocolloidal method using

electricity. It has a pH of about 6. 5 and is a natural

- deep golden color. During production, it contains 20 parts per million

hyperfine particles 99. 999% pure silver, 0. 0001 microns in diameter

electro-magnetic charge and suspended in deionized water. This is not the

to keep in the refrigerator. Silver particles in colloidal silver topovoyi >> << remain in limbo without any chemical substances, proteins,

stabilizer, or artificial additives. Typically, the antibiotic kills a half dozen >> << bacteria, but silver kills some 650. Resistant strains develop NOT

silver, as they do with antibiotics. Silver is used as a proven germ fighter

in the early 1900's. This was the basis of antibiotic treatment,

, and modern technology even better. Medical journal Lancet reported phenomenal results

colloidal silver in 1914. Dr. Henry

Crookes showed highly bactericidal colloidal silver is not quite

harmless and non-toxic to humans. Colloidal silver has been proven useful >> << against all fungi, bacteria, protozoa, parasites and some viruses

, often die within minutes. LC Ford, MD on

UCLA School of Medicine reported that in 1988 silver solutions were effective against

streptococcus, Pyogenes, Staphylococcus Aures, Neisseria

Gonorrhea, Garnerella, vaginal, Salmonella typhoid and other intestinal pathogens.

It also found that the fungicidal for Candida Albicans,

Candida Globata and M. Furfur. Science Digest said

in an article published in 1978 titled "Our Mightiest embryos Fighter", the "silver

becomes a miracle of modern medicine." Typically, the antibiotic kills

half a dozen bacteria, but silver kills some 650. Resistance

strains do not develop silver, as they do with antibiotics. Dr. Robert O. Becker

, the doctor said that "we have again the fact that silver kills bacteria

that have been known for centuries ... when antibiotics

found uses for silver as an antibiotic were discarded

".

, Term "colloid" refers to substances

which consists of tiny particles. In the true colloids, these particles

can not be seen with the naked eye, and electric charge. The particles slightly larger than molecules and is measured in microns.

This activates antibacterial quality silver >>. << "Hammer" method can be used, but

particles are too large, and the protein or other stabilizers must be included

. However, regulators may impede performance. In addition,

chemical process can be used, but the end product is usually too acid and

not so effective. Best Colloid >> << SILVER conducted electrocolloidal process that allows a

small particles of silver to be suspended in a solution of tiny charge

placed on them. This process replaces the need for any chemicals or stabilizers

product and can be called a true colloid. Then the particle

can remain in suspension almost indefinitely. Advanced Colloidal Silver

perfect deep golden-yellow color. Other products that are not true colloids

is a different color if color is added. Color

critical indicator of quality colloidal silver. Silver may be due to the proper functioning of our immune system >> << and that people with inadequate intake may be more prone to infections >>. Higher grade << colloidal silver contains

99. 999% pure colloidal silver particles

, 0. 0001 microns in diameter with a concentration of 20 parts per million

having little impact on the friendly bacteria in the digestive tract >>. << However, be aware of products with higher concentrations, they can attack

friendly bacteria, and some antibiotics. This may disappoint

, your natural balance and lead to other complications. With colloidal silver

high concentration is not necessarily better. Indeed >> << opposite is usually true. Not all colloidal silver

has the same quality. Some that I actually bought was sour >> << smell and taste awful. It is important to be careful to buy

from a trusted source when buying any food. The best rule

: do not trust the labels! - Know the manufacturer! . << >>

If the animal is sick, then by all means ...

Referring to the new estimate - that approximately 80 percent of all U.S. antibiotics are given to animals - Rep. Louise Slaughter (D-NY) again this week, bills aimed at restricting the use of certain classes of antibiotics in livestock. Massacre in lobbying their colleagues to support HR 965, the preservation of Antibiotics for Medical Treatment Act, commonly referred to as PAMTA. "Resistance to antibiotics is a major public health crisis, and still use antibiotics regularly and with minimal supervision in agriculture. As a microbiologist, I can not emphasize enough the urgency of the problem that today I am proud to once again save Antibiotics Medical Treatment Act, "said Slaughter environment. "When we go to the store to pick up dinner, we should be able to buy food without worrying that food would be subjected to our family of potentially deadly bacteria that no longer respond to our medical procedures."

The bill comes a few days after the office Slaughter reiterated the U.S. Food and Drug Administration, the percentage of all U.S. antibiotics are edible animals is much higher than previously assumed. Rep. Slaughter called the new stat "troubling" and promised to promote the legislation, which earned more than 120 sponsors. Slaughter only microbiologist working in Congress made it clear that her bill would apply only to subterapevtycheskyh use of antibiotics. "Make no mistake strattera without prescritpion, this bill does not limit the use of these drugs to treat sick animals. It simply prohibits their non-therapeutic use ", said the slaughter. "If the animal is sick, then by all means we should do them good, but routine use of antibiotics in healthy animals to promote growth of dangerously. It would be like a mother giving their son or daughter of antibiotics in their morning oatmeal. We are losing precious antibiotics. " office

slaughter and pressing economic point of view, emphasizing the use of antibiotics in food animals, as an international trade issue. "The nations of the world, including European Union countries, New Zealand, Thailand and Korea all have either been banned or start banning the use of antibiotics for growth promotion in animal feed," her office on Wednesday. "Under the rules of the WTO trading partners to implement the ban will have the right to refuse imports that do not meet this standard ... can be a great trade and economic consequences for American farmers. "

According to the Office of Slaughter, PAMTA enjoys broad coalition in support of more than 300 organizations in the scientific and medical community, including the American Medical Association, the World Health Organization and the National Academy of Sciences. Congresswoman Slaughter says she will continue to pressure the Obama administration to "take all possible measures to end the excessive use of antibiotics." Scientific Advisory

Animal Health Institute of the Council for "healthy people. Healthy animals. Healthy Planet. "The initiative also met in Washington this week. Resistance to antibiotics, and new rules to reduce the use subterapevtycheskyh were key topics of discussion for the group. Congressman Kurt Schroeder (D-OR) met with a group on Tuesday to discuss new veterinary and health issues. "I think we should become better at communicating as animal health and critical health related," said Schroeder, a practicing veterinarian and former farmer. "I am not in favor of indiscriminate use of antibiotics, no one here," said Schroeder, adding that regulators should be careful in writing the rules to avoid unintended negative consequences of humans and animals. .

Alcohol is metabolized mainly in the liver ...

In reviewing the effects of antibiotics and alcohol is important to see how they both affect the body. Then realized it was easier to understand how they work in conjunction with each other. When trying to decide about mixing alcohol and antibiotics, is that it can be done to know the dangers. Antibiotics are through blood flow in the affected region, where they work to cure the infection in the organ or tissue. Antibiotic, ultimately metabolized by enzymes and excreted from the body. PP Alcohol also passes through the blood, which delivers it to the brain where it can lead to intoxication. Alcohol is metabolized mainly in the liver and then excreted from the body. When antibiotics and alcohol mix alcohol in the blood can reduce the effectiveness of antibiotics, so that by the time he reaches the infected area it will not be healing energy needed to treat disease. Adding alcohol can lead to risk of disease gets worse, even continuing to antibiotics. Alcohol does not always interact badly with antibiotics, but the circumstances are unlikely to come up with any positive effect. In the case of a dangerous disease, it can lead to serious results. Not all antibiotics, but levels vary in composition, and will interact with alcohol differently. There are several types that should never be mixed with alcohol because they have other serious side effects, but lower efficacy for treatment. P Some of these side effects increase irregular pulse, low blood pressure, vomiting, lack of breath and headaches. When taking antibiotics, it makes sense to turn to a doctor about any possible side effects that antibiotics and alcohol, probably mixed up in the blood. Alcohol by itself will reduce the natural healing power suits, so this is another good reason for not when you are sick. Drinking can reduce white blood cells and overalls energy, leading to delay the healing process. When patients are usually better to wait until you feel better before you start drinking. Alcohol and antibiotics do effect a person will vary from person to person, as all the individual metabolism is different. There are reports about people who mix two for minor problems such as infected cuts, and felt no negative effects at all. They also reported that, apparently, the drug quickly helped cure the infection. Others, though reported suffering from a huge headache and nausea the next day. Usually it is better safe than sorry and not drink anything, even if the doctor says, there can be no side effects as a result of mixing the two. The general opinion of strattera dosage experts of mixing antibiotics and alcohol is that it is better not to do. Even antibiotics that are considered safe to take while drinking a lot of variables, not real guarantees can be given to positive results. Some antibiotics are known to have negative side effects and they should never be taken at the time. .

Comparison of protein sequences of hsp70

Archaea are now recognized as one of two main areas of prokaryotes [1, 2]. Most of the genes that show

archaea, distinct from bacteria to transfer information processes such as DNA replication, transcription and translation [3, 4]. Of these, DNA replication machinery is very different between the two domains [5]. In terms of transcription, the basic units of RNA polymerase (s) are the same as in

Bacteria and archaea,

archaea but also contains several smaller units and some transcription factors not found in bacteria. Most of the components of translation machinery, which includes various rRNA, r-proteins, the main factors, elongation, and various amino acids, enzymes, and tRNA charging, etc., usually common to both bacteria and archaea [3, 6] . In addition, Mr. proteins in archaea >> << are also located in operonov similar to that observed in bacteria. But

archaea differ from bacteria in some unique R-proteins and initiation factors of translation. Archaea differ from most bacteria in their cell membrane and cell wall composition [1, 2, 7]. (Fig. 1)

Fig. 1 Comparison between the shell membrane prokaryotes. However, besides these differences,

archaea are widely similar to bacteria. Most of the metabolic pathways that make up the vast majority of all the repertoire of genes of an organism, are common between

archaea and bacteria [8]. In terms of their structure cells

archaea do not differ from gram-positive bacteria. In prokaryotes, only these two groups of organisms are buy strattera limited by a lipid membrane unit [9-11], and they usually contain thick sakkulyusa different chemical composition [12]. Some

archaea also show positive staining gram-negative and some of them (namely, Thermoplasma), similar to certain Gram-positive bacteria (eg mycoplasma) do not contain cell wall [2]. The similarity of archaea and bacteria spread to many other characteristics, including cell size significantly smaller (100-1000 times) than in eukaryotic cells lack nuclei, cytoskeleton, histones, spliceosomal introns, circular organization of their genomes, the organization of genes in the operon, the presence of 70S ribosomes, etc. [13] Kunyn et al. [8] showed that about 63% of genes in

M. janaschii in other bacteria, whereas only 5% of them clearly with Eukarya. Although about 1/3 of the total genes in the archaea >> << are unique (ie not see the similarity with other organisms), the same is true for most other prokaryotic genomes. Rice. 2 Comparison of protein sequences Hsp70 >> << In phylogenetic trees based on several different proteins archaea species show polyfyletycheskoho branching in gram-positive bacteria. [14-16] If we consider only prokaryotycheskyh homologues, the phylogenetic tree for the majority of proteins showed that archaea

more closely related to gram-positive bacteria (eg, monoderm bacteria, which include

Thermotoga) than Gram-negative bacteria (unpublished results). [9] evidence for closer relations between

archaea and gram-positive bacteria compared to gram-negative bacteria, also provided a number of known sequences of signature (ie, 21-23 aa INDEL in Hsp70 (Fig. 2) and 26 aa INDEL in GS I), which are usually clearly divides these two groups of prokaryotes. [9, 17]

Fig. Image 3 Kendler in universal ancestors

Questions can now question how these differences between archaea and bacteria possibly originated and how these two groups relate to each other? Since most genes that show

archaea must be separated from the bacteria to processes of information transfer, and these processes are of fundamental importance, it is suggested that these differences arose in the universal ancestors to the separation of these two areas. Vouz and Kendler [18, 19] believe that these two areas as well as eukaryotic cells evolved from pre-mobile community, which contain different types of genes in the process that led to the fixing of a specific subset of genes in the ancestors of these areas. These previous cellular entities posited, have a stable genealogical or chromosomes, and no typical cell membrane, which allows unlimited lateral translation of genes [18, 19]. Under these proposals all the differences between the

archaea and bacteria arose in an earlier stage of cell Darwin without money, but they offer no reason as why there are differences between the two groups emerged or developed. Cavalier-Smith [20] suggested the possibility

archaea development of gram-positive bacteria, as adaptation to hyperthermophily or increased acidity, but it does not explain how the various differences in the genes, information transfer that distinguish

archaea from bacteria emerged. Gupta [9, 10] proposed an alternative proposal to explain the striking similarity between archaea and saw the gram-positive bacteria, the cell structures in different phylogeny of genes and several other important observations. An important characteristic of archaea >> << that they are resistant to broad spectrum antibiotics, which are mainly produced by gram-positive bacteria [9]. These antibiotics affect genes (namely transmission of information or processes and synthesis of cell wall and membrane components), which primarily provide

archaea from bacteria. These observations are central to understanding the origin of Archean >>. If << differences that characterize

archaea from bacteria developed in the pre-cellular phase

it is difficult to understand how archaea evolved resistance to various antibiotics produced gram-positive bacteria [21, 22]. It appears also that too many matches that the majority of genes that distinguish

archaea from bacteria provide the main purpose of these antibiotics. In the table above describes the sites of action of antibiotics. The majority of known antibiotics produced by gram-positive bacteria

To explain these observations, Gupta suggested that the first groups of prokaryotes, which evolved, were associated with gram-positive bacteria [9, 10, 21, 22]. Features that distinguish

archaea from bacteria and not develop independently of each other on stage precellular derived from gram-positive bacteria, in response to antibiotic selection pressure. In one likely scenario, after a group of gram-positive bacteria designed to conduct various kinds of antibiotics to survive in this highly selective environment of some bacteria has undergone significant changes in genes that are to these antibiotics. The changes leading to resistance were different species, including mutations, insertion / deletion, not homologous recombination, and gene-replacement targets with non orthological genes. The long and consistent elections in various antibiotics containing environment led to the eventual development of sustainable strain, which has undergone significant changes in many genes that were the objects of these antibiotics and this strain is a common ancestor of modern

archaea [9, 10, 21, 22]. The evolution of archaea >> << in response to antibiotic selection also provides a plausible explanation for their adaptation to harsh environments such as high temperature, high salt or high temperature and acidity, etc. It is assumed that these devices were defensive strategies to find niches that are hostile to antibiotics of organisms [9, 10, 21, 22]. Thus, unlike other proposals, this proposal can logically explain the evolution of the most distinctive characteristics of Archaea

known groups of bacteria normal evolutionary mechanisms, without attributing such differences in the unusual properties of the universal ancestor. Because these differences between

archaea and bacteria have evolved at a very early stage in the history of prokaryotes (Fig. 4), archaea

appear different from bacteria in phylogenetic trees based on these characteristics. Interestingly, in this context that the analysis of genomic sequences on the lake and his colleagues argue that the root of the tree of life does not lie either in archaea [23] or Gram-negative (diderm) bacteria [24]. .

Intestinal bacteria are commonly used in ...

Koliformnyh bacteria are widely used as health food and water. They are defined as bacillary

without the bacteria that can ferment to form acid strattera dosing and gas when incubated at 35-37 ° C. Coli-forms can be found in the aquatic environment, in soil and on plants, they are universally present in large quantities in feces of warm-blooded animals. While coliforms themselves generally do not cause serious diseases, they are easy to culture, and their presence is used to indicate that other pathogenic organisms of fecal origin may be present. Fecal pathogens include bacteria, viruses, protozoa or multicellular and many parasites. ,

(E. coli), bacillary member of E. coli may be different from most other bacteria koliformnyh the ability ferment lactose at 44 ° C in test >> << and its growth and color reaction to certain types of media culture. When cultured on EMB plates positive for E. coli

metallic green colonies on dark purple media. Unlike the common intestinal group

E. coli almost exclusively fecal origin and their presence is as effective proof fecal contamination. Some strains of E. coli

can cause serious disease in humans. .

Buddelmeijer

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N, J. Bekvit complex Escherichia coli cell division proteins

FtsL, FtsB and FtsQ forms independently of its localization

wall region. (2004) ... Buddelmeijer

N, J. Bekvit Assembly of cell division proteins in E. coli cells << center. Opino >> Curr Microbiol. 5 :553-557 (2002) ... Buddelmeijer N, Judson

N, D Boyd, Mekalanos JJ, J. Bekvit YgbQ, protein cell division

in Escherichia coli and cholera, localizes

spivzalezhnyh in fashion with FtsL to section of the site. Labor Academician Natl

Research U.S. A. 99 :6316-6321 (2002) .. Chen JC, Minev M, J. Bekvit Analysis of ftsQ mutant alleles in Escherichia coli:

addition, partition location, and work in processing proteins >> << cell division. J. Bacteriol. 184 :695-705 (2002) ... Chen JC, J. Bekvit FtsQ, FtsL and FtsI require FtsK, but not FtsN for participating in the localization of FtsZ

in E. coli cell division. Mol Microbiol. 42 :395-413. (2001) ... Hiho, J.-M. , Bekvit, J. Cell

division in Escherichia coli: >> << role of FtsL domains in septum localization, function and oligomerization. J. Bacteriol. 182 :116-129. (2000) .. Weiss DS, Chen JC, Hiho JM, Boyd D, Bekvit

J. Localization of FtsI (PBP3) to the septum ring

requires the membrane anchor, the ring Z, UFNS, FtsQ and

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(1999). Chen JC, Weiss DS, Hiho JM, J. Bekvit wall localization of FtsQ, essential cell division protein

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(1999) .. Weiss, DS, Pogliano K. Carson, M. Guzman, L.-M.

, Fraipont C., Nguyen-Distche, M., Losick, R.,

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