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WO2002040511A2 - Sequence d'adn et microcine de la souche dsm 6601 d'escherichia coli - Google Patents

Sequence d'adn et microcine de la souche dsm 6601 d'escherichia coli Download PDF

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Publication number
WO2002040511A2
WO2002040511A2 PCT/EP2001/012937 EP0112937W WO0240511A2 WO 2002040511 A2 WO2002040511 A2 WO 2002040511A2 EP 0112937 W EP0112937 W EP 0112937W WO 0240511 A2 WO0240511 A2 WO 0240511A2
Authority
WO
WIPO (PCT)
Prior art keywords
control center
components
repeaters
information
channel
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP2001/012937
Other languages
German (de)
English (en)
Other versions
WO2002040511A9 (fr
WO2002040511A3 (fr
Inventor
Jörg Hacker
Gabriele Blum-Oehler
Günther Jung
Klaus Hantke
Silke Patzer
Felipe Moreno
Fernando Baquero
Rosario Baquero
Daniel Bravo
Ulrich Sonnenborn
Jürgen Schulze
Hans Proppert
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pharma Zentrale GmbH
Original Assignee
Pharma Zentrale GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pharma Zentrale GmbH filed Critical Pharma Zentrale GmbH
Priority to AU2002237220A priority Critical patent/AU2002237220A1/en
Publication of WO2002040511A2 publication Critical patent/WO2002040511A2/fr
Publication of WO2002040511A9 publication Critical patent/WO2002040511A9/fr
Publication of WO2002040511A3 publication Critical patent/WO2002040511A3/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
    • C07K14/24—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Enterobacteriaceae (F), e.g. Citrobacter, Serratia, Proteus, Providencia, Morganella, Yersinia
    • C07K14/245—Escherichia (G)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Definitions

  • the present application relates generally to components, such as repeaters, in a mobility network and, more particularly, to a technique for performing operations, administration, and maintenance of such components.
  • FIG 1 shows a prior art mobility network or cellular telephone system 10 for mobile communications.
  • the system 10 includes a control center 12, a mobile switching center (MCS) 14, abäse Station Controller (BSC) 16, and multiple base transceiver stations (BTS) 18, 20, 22, also called base stations or cells.
  • the control center 12 is for Controlling the network 10 and for monitoring Performance ofthe other network components, as further described below.
  • the MCS allows for. communication to other networks, such as the PSTN, ISDN and other data networks.
  • the BSC is one of many in a base station subsystem (other BSCs not shown) and controls multiple of BTSs.
  • Each BTS is coupled to a communication tower or antenna 24 for transmitting and receiving signals from mobile stations (e.g., a cellular phone), such as mobile station 26.
  • the towers are strategically placed on buildings or along roadways in high-traffic areas.
  • One ofthe base stations is typically designated as a donor cell and is coupled to multiple repeaters.
  • the donor cell is shown as BTS 20 and is coupled to repeaters 30, 32, and 34, by means of cable or wireless means.
  • Repeaters are an economical alternative to expand coverage area while minimizing the number of towers .. Specifically, repeaters are small electronic devices used to boost and amplify transmitted and received signals that have weakened because the signal has decayed over distance. Repeaters may also be used to retransmit signals in segments of roads that signals cannot otherwise penetrate, such as in tunnels.
  • Repeaters generally only have sufficient power to cover short distances (e.g., 100 meters) and are often coupled to directional antennas, such as shown at 36.
  • repeaters also may be coupled to other communication towers, as shown at 38.
  • the control center 12 periodically polls the components on the system 10 to ensure that all the components are operating properly. For example, the components may be checked to determine whether they are on or off and whether they are working properly. There are a variety of reasons that the Controller may check the components and such reasons are generally termed in the art as operations, administrative and maintenance operations.
  • the Controller sends the request through the donor BTS 20.
  • the repeaters are coupled to the BTS using dedicated traffic Channels, shown at 40, and a separate Channel or wire 42 for polling to obtain or perform administrative operations, alarm monitoring, control, maintenance, and diagnostic procedures (collectively called operations, administration and maintainance (OA&M)). This operational or diagnostic information is transferred through the network to the control center for analysis.
  • OA&M operations, administration and maintainance
  • the present invention eliminates the need for a dedicated channel or resource to perform such operations on system components.
  • the existing control channel is used for performing OA&M.
  • address information is put into the message on the control Channel to uniquely communicate with desired system components.
  • FIG. 1 is a prior art mobility system having a dedicated line for performing
  • FIG. 2 is a diagram illustrating a mobility System according to the invention that uses a control Channel to perform OA&M on system components.
  • FIG. 3 is a flowchart of a method for performing OA&M on System components in a mobility network.
  • FIG. 2 shows a system 60 according to the invention.
  • the system 60 includes a control center 62, a mobile switching center 64, a base station controller 66, and multiple base stations 68, 70 and 72, which are all connected as previously described.
  • the mobile switching center, base station controller, and base stations collectively form a mobile network.
  • Multiple system components 74, 76 and 78, are coupled to the donor cell (base station) 70 through communication Channel 80.
  • the communication Channel 80 may be a cable, such as a coaxial cable or fiber-optic cable, or may be a wireless connection scheme.
  • no additional resources (such as dedicated Channel 42 from FIG. 1) are needed to communicate with the components 74, 76 and 78.
  • the components 74, 76 and 78 may be repeaters or any third-party components , such as smart antennas.
  • the base station 70 includes many radio channels for communicating with other components.
  • the base station includes traffic channels and a common control channel.
  • the control Channel is created to set up links bet een the telephones that are parties to the call.
  • control channel initiates the ringing ofthe requested phone or mobile station. Once the call is properly set up, the control channel is torn down and the traffic channels for communication are established. It is this control Channel that is used to perform OA&M on system components 74, 76 and 78.
  • FIG. 3 shows a flowchart of a method for implementing the OA&M on a system component.
  • the control center sends a request for Performance information of a component on the network.
  • the control center 62 may wish to poll or request the component 74 to send the information at periodic intervals to ensure that it is properly operating. To accomplish this, the control center 62 sends the request to the mobile network.
  • the request may be sent to the base station controller 66 within the base station subsystem.
  • the mobile network reformats the request for transmission over the digital control Channel (DCH).
  • DCH digital control Channel
  • the mobile network includes address information of the component into the request on the control channel.
  • the base station controller inserts the address information and puts the request on the digital control channel. The request is then forwarded to the donor cell base station 70 and retransmitted to the component.
  • the component receives the request on the control Channel and responds with the requested information. Typically, in responding to the request, the component puts its own address information first followed by a data, such as Status.
  • the mobile network forwards the requested information on to the control center 62.
  • the requested information is received by the base Station Controller and resent to the control center.
  • the system provides all over-the-air repeater administration, alarm monitoring, operations and element control with Connectivity specifically residing on a repeater 's donor cell common shared Channel resource (traffic or control) and passed between subsequent repeaters on the repeater simulcast common shared channel resource.
  • Connectivity specifically residing on a repeater 's donor cell common shared Channel resource (traffic or control) and passed between subsequent repeaters on the repeater simulcast common shared channel resource.
  • the OA&M Connectivity to subsequent repeaters in any type of simulcast or series configuration will continually reside on the common shared
  • the invention takes advantage ofthe common shared Channel transport ability ofthe wireless network to establish a connection to the control center over the network that is being repeated without taking away capacity from the traffic.
  • Competitive consumer electronics level pricing will quickly be established for compatible transceivers so that this telemetry information transport can be added very easily and inexpensively to these repeaters.
  • a "heartbeat" can be obtained from the repeater, assuring that it is still operating.
  • detailed operating measurements and reports, as well as instructions (e.g., change parameters or settings) and controls can be sent over the same administration link.
  • EDGE-GPRS which would also use a data control channel.
  • control Channel is generally used to carry the OA&M information
  • other Channels that are already used for communication with the mobile stations also may be used, such as the traffic Channels and Channels that are broadcast to the receivers.

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Communicable Diseases (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Biochemistry (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Genetics & Genomics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Peptides Or Proteins (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Mobile Radio Communication Systems (AREA)

Abstract

L'invention concerne une séquence d'ADN présentant la suite de nucléotides représentée à la figure 1, le peptide codé par ladite séquence, des dérivés de ce peptide ainsi que l'utilisation de la séquence d'ADN, du peptide et des dérivés dudit peptide.
PCT/EP2001/012937 2000-11-10 2001-11-08 Sequence d'adn et microcine de la souche dsm 6601 d'escherichia coli Ceased WO2002040511A2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2002237220A AU2002237220A1 (en) 2000-11-10 2001-11-08 Dna sequence and microcine from escherichia coli strain dsm 6601

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10055789A DE10055789A1 (de) 2000-11-10 2000-11-10 DNA-Sequenz und Microcin aus Escherichia coli StammDSM 6601
DE10055789.9 2000-11-10

Publications (3)

Publication Number Publication Date
WO2002040511A2 true WO2002040511A2 (fr) 2002-05-23
WO2002040511A9 WO2002040511A9 (fr) 2002-07-25
WO2002040511A3 WO2002040511A3 (fr) 2002-12-05

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2001/012937 Ceased WO2002040511A2 (fr) 2000-11-10 2001-11-08 Sequence d'adn et microcine de la souche dsm 6601 d'escherichia coli

Country Status (3)

Country Link
AU (1) AU2002237220A1 (fr)
DE (1) DE10055789A1 (fr)
WO (1) WO2002040511A2 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7601511B2 (en) 2003-11-12 2009-10-13 University Of Georgia Research Foundation, Inc. Biotin-facilitated transport in gram negative bacteria

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
AZPIROZ MARIA F ET AL: "The structure, function, and origin of the microcin H47 ATP-binding cassette exporter indicate its relatedness to that of colicin V." ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, Bd. 45, Nr. 3, M{rz 2001 (2001-03), Seiten 969-972, XP002207827 ISSN: 0066-4804 *
BLUM ET AL: "Properties of Escherichia coli strains of serotype O6" PLASMID, NEW YORK,NY, US, Bd. 23, Nr. 4, 1. Juli 1995 (1995-07-01), Seiten 234-236, XP002085750 ISSN: 0147-619X *
DOBRINDT ULRICH ET AL: "S-fimbria-encoding determinant sfaI is located on pathogenicity island III536 of uropathogenic Escherichia coli strain 536." INFECTION AND IMMUNITY, Bd. 69, Nr. 7, Juli 2001 (2001-07), Seiten 4248-4256, XP002207828 ISSN: 0019-9567 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7601511B2 (en) 2003-11-12 2009-10-13 University Of Georgia Research Foundation, Inc. Biotin-facilitated transport in gram negative bacteria

Also Published As

Publication number Publication date
AU2002237220A1 (en) 2002-05-27
WO2002040511A9 (fr) 2002-07-25
WO2002040511A3 (fr) 2002-12-05
DE10055789A1 (de) 2002-06-06

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