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examples function through a cell wall lytic mechanism4 The most prominent example is lysostaphin, a poly-functional hydrolase originally identi ed in S simulans that targets rival species/strains of staphylococci (Kumar 2008) In light of the growing resistance to traditional antibiotics, lysostaphin has received considerable attention as a possible weapon against Methicillin-resistant S aureus (MRSA) and nonMRSA isolates of S aureus Comparable enzymes, namely millericin B and zoocin A, have been isolated from streptococcal strains (Beukes et al 2000; Akesson et al 2007) Such proteins serve as an important reminder that the enzybiotics eld encompasses more than phage lysins alone, and necessitates that future screening techniques cast a large net in search of novel antibiotics Broadening the spectrum further still, phage themselves can encode peptidoglycan hydrolases in addition to lysins proper Putative enzymatic motifs are often present within proteins of the phage tail assembly (Kanamaru 2002; Kenny et al.

= 2Re(Ee:(i)g[z(i)]),

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further, the probability to reside in state i for exactly m consecutive time steps equals (1 - pi i)pE- , that is, there are m - 1 steps in which the possibility (staying in i) with probability pi,; is taken, and one final step with probability 1 - pi,; where indeed a step leaving state i as a success and staying towards another state j # i is taken. Interpreting in state i as a failure (one fails to leave) we see that the state residence times in a DTMC obey a geometric

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where P is the magnitude of the initial momentum, P = m,dR/dt, and b is the impact parameter. These are the equations of motion for the system and give a complete dynamical description of R(t)and cp(t)in terms of the interaction potential and the two parameters P and b characterizing the collision. By combining (7.38) and (7.39), we obtain (7.40) Because (7.40) contains no terms in p, it can be regarded as a description of the one-dimensional motion of a particle in an effective potential, (7.41) which contains a centrifugal contribution in addition to the interaction potential. According to Figure 7.4, the scattering angle 8 can be obtained via ( r - 8)/2 from the position of the scattered particle at the closest approach to the target. The condition of minimum distance is given by dR/dt = 0, and, from (7.40), we hence obtain

2004; Piuri and Hatfull 2006) or even the head (Moak and Molineux 2004), presumably to facilitate the initial injection of viral DNA And although it is not their natural purpose, recent evidence has shown that these enzymes can lead to Grampositive lysis when added exogenously Rashel et al (2008) identi ed a tail-associated protein from the genome of an S aureus phage that contains two putative lytic motifs; when individually expressed and puri ed, both domains induced staphylococcal death Despite these ndings, no tail enzymes have ever been identi ed during a functional screen of a phage genome (to our knowledge) Several reasons could underline this discrepancy for instance, some enzymes might require the presence of the entire macromolecular tail assembly for proper activity.

About Adobe AIR............................................................................................................1228 Installing AIR into Dreamweaver ...................................................................................1230 Designing for AIR ........................................................................................................... 1231 Packaging Your AIR Application .....................................................................................1235 Summary ........................................................................................................................ 1241

port, typically a DA-9 port, a parallel port, or a game port. The DB-25 connector is also popular on external modems and serial printers.

Moreover, structural lysins often represent component domains within much larger polypeptides; in the context of a functional screen, these domains would not be expressed individually and the bulk proteins could prove dif cult to obtain due to their size Nevertheless, if future research could reliably harness the enzymatic activity of tail lysins, it would represent another promising avenue within the enzybiotics eld In addition to this possibility, phage tail proteins are also of considerable interest for their ability to traverse the other components of the bacterial cell envelope These include the outer membrane of Gramnegative bacteria and the mycolic acid layer of mycobacteria, structures that act as formidable obstacles to lysin treatment While it is true that several reports have documented the use of lytic enzymes against viable Gram-negative organisms (Alakomi et al 2000; Morita et al 2001a; Kim 2004; Briers et al 2008), this activity was generally either.

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