Bacteriophage Lambda


Infection begins when a phage adsorbs to the lamB gene product, a receptor in the outer membrane of E. coli. The phage stores its DNA under pressure and so it can be injected into the cell, with the help of a cellular protein – ptsM. The DNA in the phage’s head is linear and double stranded but it has 12 base complementary single strang overhangs on each 5’ prime end, rich in G and C. These “sticky ends” mean that the DNA rapidly circularises. In most circumstances cII levels in the cell will not be high and so the phage will enter the lytic cycle typical of bacteriophages.

Lytic cycle

Immediate early (IE) stage

The phage’s lytic cycle uses three promoters PL, PR and PR’. These need to be strong promoters so that they can recruit the host polymerase. The host polymerase binds preferentially to these promoters to such an extent that if many copies of the promoters are artificially inserted the cell is unable to transcribe its own DNA and dies. PL promotes a transcript which initially terminates after transcription for N, an anti-termination protein. Transcription from PR produces cro, which is important in continuing the lytic cycle rather than lysogeny (see cI section). The PR’ transcript at this stage only produces a small inactive protein.

Figure 1: Immediate early stage
(click on any diagram to enlarge)

Delayed early (DE) stage

The immediate early stage produces the anti-termination factor N. There are areas around the PL and PR promoters called N utlilisation sites or nut sites. They cause N to bind to the transcriptional apparatus at the promoter. This prevents some of the the early termination that occurs in the immediate early stage. Most importantly for lysis, it allows the transcription of O, P and Q. O and P are needed for DNA synthesis to occur – they recruit the host’s machinery for DNA replication to a point near their locus. P prevents the host from synthesising bacterial DNA, working with cII. The machinery produces a number of copies of the phage’s circular DNA, each of which is used in rolling circle replication to produce around 10 phage genomes. Q is an anti-termination factor needed for progression to the late stage. Although int is part of the PL transcript, integrase is not synthesised because the transcript also contains the sib region which folds in a hair-pin loop and results in this section of the transcript being cleaved by RNaseIII.

Figure 2: Delayed early stage

Luzzati first showed that N was an anti-termination factor. He used a mutant lysogen which had a defect in N and a temperature sensitive transcriptional repressor which allowed transcription from PL and PR at 30ºC but not 40ºC. He superinfected the lysogen with a phage providing N at 30ºC but no transcription of the DE region of the original prophage took place. It was not until the temperature was raised to 40ºC that transcription began from PL and PR and was allowed to continue without termination by N, producing both IE and DE products. This proved that N did not create new promoters around the DE region but acted as an anti-termination factor.

Late stage

Once replication of the phage DNA has been initiated the other components of the new phages, heads and tails, are needed, as well as proteins for lysis. Q extends the PR’ transcript by binding to the transcriptional apparatus at a Q utilisation (qut) site close to the promoter. Once Q is bound termination does not occur as easily and so S, R and a number of genes coding for the heads and tails of the phage particles are transcribed. The head and tail proteins self assemble. R is an endolysin which is needed to cleave the cell wall for lysis.

Figure 3: Late stage

S produces mRNA with dual start sites for translation: one of these start sites produces S105, a holin; the other produces S107 which has an additional basic residue and acts as an antiholin because it cannot interact with the intact membrane correctly. Holin is produced twice as frequently as antiholin but binds preferentially to the anti-holin. This means that half of the holin molecules are disabled by antiholin. It is believed that this mechanism allows the sudden and rapid creation of many holes after a delay. Initially many S products are produced but there are few functional holin-holin dimers, not enough to create a single hole. When enough holin-holin dimers aggregate to form a hole in the membrane, its properties change and allow S107 to function as a holin. This immediately triples the number of S products available for hole creation, allowing rapid lysis.


λ has an alternative lifestyle to the violence of lysis. It can integrate into the host’s genome and form a stable lysogen which continues to grow and divide. This is a stable state, even superinfection by the same phage willnot lead to lysis. There are some related phages which are heteroimmmune (e.g. 21 and 434); these can infect lambda lysogens and trigger lysis. Various experiments have been done to hone in on the ‘immunity substance’that provides protection from self superinfection.

Hfr strains of E. coli lysogenic for λ can be mated with wild type bacteria. They do not form recombinants, the Hfr strain transfers it’s entire genome and the prophage becomes lytic (zygotic induction). If the wild type cells are first made lysogenic then recombinants are formed. This demonstrates that the immunity substance is a cytoplasmic factor. In another experiment, λ is added to a population of E. coli cells on a petri dish. A turbid plaque is formed for wildtype λ which is made up of lysogens and periodically some lysis. Mutations in some genes (cI, cII and cIII) give clear plaques, meaning that all cells have gone into lysis. Every one of these factors is needed to establish lysogeny. Using temperature sensitive mutations to each gene it has been shown that only cI is needed to maintain lysogeny once established. It is the repressor, or immunity substance. A very few mutants are unable to establish lysogeny even in the presence of cI and always go into lytic cycle, these are dubbed virulent.

cI was isolated using a double labelling experiment. Wild type phage protein was labelled with one radioactive amino acid marker and protein from a cI strain was labelled with another. Proteins were pooled and separated by chromatography. The protein fraction which only had the wildtype label was cI. This was confirmed by the fact that it did not bind to the DNA of virulent mutants.


The ultimate factor which determines whether λ will go into a lytic or lysogenic cycle after infection is the level of cII in the cell. If cII levels are high enough a lysogen will be formed, otherwise a lytic cycle will ensue. But cII is broken down by ftsH, a protease. cIII inhibits ftsH by binding to it competitively and so allows cII levels to remain high. This is why both cII and cIII are essential for the establishment of lysogeny.

Figure 4: Initial establishment of lysogen – cII active but low cI

cII is a transcriptional activator which acts on three promoters, PRE, Pint and PQ’. PRE promotes a transcript which produces cI and also the antisense to the normal mRNA to cro (which is being transcribed as usual in the delayed early stage.) This is important as it binds to the sense mRNA and prevents translation. PQ’ performs the same task for Q. This is necessary to stop the extension of the PR’ transcript which would send the cell into lysis. Pint has a short transcript which is translated to an integrase. Since it is not affected by N it terminates before the sib region and so no hairpin loop forms, so the RNA is not a target for RNase III.


The areas around PL and PR are the operators OL and OR. These allow control of the promoters: each has three sites to which transcription factors can bind. cI forms a dimer and binds best to site 1, then site 2 and worst to site 3. When it binds to OL1 it is well positioned to interact with other cI dimers to allow them to bind cooperatively to OL2. Once these two sites are bound, transcription from PL is repressed. This is important to prevent xis being produced which would excise the integrated prophage, and generally to avoid a waste of resources on unnessessary products. There is a similar story for OR, with initial binding to OR1 and then cooperative binding to OR2. But here the binding to OR2 activates another promoter PRM in addition to repressing PR. Repression of PR stops the production of Cro and Q, removing the dependence of the phage on PRE and PQ’ (and hence cII) and prevents O and P from initiating replication on the integrated genome.


Figure 5: Lysogenic state – cII levels now low, cI levels at optimum

PRM is the promoter for the maintenance for lysogeny. Its transcript produces cI, which we have established is the only factor needed to maintain the lysogenic state. In lytic state thispromoter is repressed by the action of cro which cannot bind cooperatively and binds best to OR3.This is why cro levels must be kept down for lysogeny. At very high concentrations in lytic cells, cro will bind to OR2 and OR1 to regulate its own production by negative feedback. cI has a similar regulatory mechanism, at high concentrations it will bind to OR3 and so repress PRM.

Integration and induction

The integrase produced by the Pint transcript results in the insertion of the prophage at attB, which lies between the galactose catabolic operon and the biotin biosynthetic operon. The inserted prophage is a circular permutation of the phage DNA in the particle, with int on one side and the sib region on the other.Once inserted the prophage will be replicated with the rest of the bacterial genome and so lie dormant, being passed into all the bacterial progeny.

In general the lysogenic state is observed to be very stable, 1 in 105 cells would normally go into lysis in a culture. This process is called induction. Lysis can be reliably induced by exposure to UV light. This damages DNA, which is one of the triggers for the cell’s SOS response – a postreplication mechanism for DNA repair.The genes for the SOS response are repressed in normal cells by a dimer called lexA. In the SOS response, recA is made active by binding to single stranded DNA and cleaves lexA, removing the repression.But cI has the same motif that makes lexA a target for cleavage and so in lysogens it is cleaved too.

cI levels fall and so cI no longer binds to the operators; PR and PL are no longer repressed. PRM is no longer activated so no further cI can be made. The situation now looks very like Figure 1 except that the DNA is now part of the bacterial genome and not a small loop of phage DNA. The same process happens – N istranscribed which allows the elongation of the PR and PL transcripts. The PL transcript no longer has the sib region because of the circular permutation, and so no hairpin loop is formed and RNase III attack does not occur. This means that xis (and int) are expressed. Both these factors and a bacterial gene product called fis are needed to allow excision. The excised circular DNA proceeds as in the lytic cycle.

Figure 6: Induction of a lysogen – cI has been cleaved

Lysis or lysogeny?

Not all the factors that influence the levels of cII – and so the fate of an infected cell – are understood. The nutritional status of cells is certainly important and there are proteases other than ftsH which can breakdown cII and are regulated by the cell cycle. Although a model organism for the study of bacterial infection, λ still holds its mysteries.

39 thoughts on “Bacteriophage Lambda”

  1. Nice way of presentation understandable If supported by animation would have been batter.particularly lysogenic and lytic state.

  2. you have saved me from failing a genetics module of my degree… thankyou so so much… I owe u a pint

  3. Thanks a lot for sharing this with all of us you actually understand
    what you are speaking approximately! Bookmarked. Please additionally discuss with my site
    =). We could have a link exchange agreement between us

  4. Here are a few statements released by public health experts.
    They are good about replacing dead atomizers
    when they are defective. Since my discovery, I try to store my
    NJOY electronic cigarettes in cold places whenever possible, and I noticed
    it has definitely extended the life of my NJOYs.

  5. Hi, Awesome posting. You will find there’s difficulty using your web site with internet explorer, might test that? IE ‘s still industry key in addition to a very good part of people will abandon a person’s superb creating due to this dilemma ??????????? ??????? ?????????.

  6. Hi, ?t? nice piece of writing ?bout media print,
    ?e ?ll understand media ?s a wonderful source ?f f?cts.

    Here ?s my weblog – aras-reisen.e? (Aaron)

  7. You actually make it appear so easy with your presentation but I
    in finding this topic to be really something which
    I believe I would never understand. It sort of feels too complex and extremely vast for me.
    I’m taking a look forward on your subsequent publish, I’ll try to
    get the grasp of it!

  8. I have been to probably a dozen wegdnids but never caught a bouquet. Like you I found that there were so many rules and everything seemed so formal that I did not feel at ease. When my husband and I got married we keep everything very simple and informal. It was fun and the guests seem to have had a good time. We tried to make sure everyone was comfortable and relaxed.

  9. Most of opportunities, if you ask a boy what he
    finds more difficult between walking to a girl in a public place
    and start talking and a phone conversation, they would certainly agree
    on the fact that women are too rough by phone and reverse phone lookup chats with them are to be avoided as a paramount element.
    Although native to Central and South America, this plant
    can be found in most tropical climes, usually in disturbed land around construction sites,
    orchards and agricultural land. This ironic little accessory also comes with a one of three power stones; rose quarts,
    crystal, or amethyst.

  10. Superb website you ?ave ?ere b?t I ?as woondering if ?ou knew of any message boards that cover the ?ame topics talked ?bout in t?is article?
    I’? ?eally likke t? be ? ?art ?ff group wh??e I ?an g?t advice f?om other experienced individuals that share th? same inter?st.
    If y?u haave any suggestions, pleas? let me know.

    Bless you!

    Silahkan Cek halaman website Saya demi dapat Info Menarik tentang jas murah .


  11. When someone writes an post he/she retains
    the plan of a user in his/her mind that how a
    user can know it. So that’s why this paragraph is amazing.

  12. Have you ever thought about adding a little bit more than just your articles? I mean, what you say is valuable and everything. Nevertheless think of if you added some great pictures or video clips to give your posts more, “pop”! Your content is excellent but with images and video clips, this blog could definitely be one of the best in its field. Good blog!

  13. Definitely believe that that you stated. Your favourite reason appeared to be at the web the simplest factor to understand of. I say to you, I certainly get irked even as other folks consider worries that they just do not recognise about. You managed to hit the nail upon the highest and also outlined out the whole thing with no need side-effects , other folks could take a signal. Will probably be again to get more. Thank you

  14. Please let me know if you’re looking for a writer for your blog. You have some really great articles and I feel I would be a good asset. If you ever want to take some of the load off, I’d really like to write some content for your blog in exchange for a link back to mine. Please blast me an email if interested. Regards!

  15. Thanks for the good writeup. It in reality used to be a entertainment account it. Glance complex to more delivered agreeable from you! However, how can we keep up a correspondence?

  16. I loved as much as you will receive carried out right here. The sketch is tasteful, your authored subject matter stylish. nonetheless, you command get got an impatience over that you wish be delivering the following. unwell unquestionably come more formerly again as exactly the same nearly a lot often inside case you shield this increase.

  17. Howdy I am so excited I found your webpage, I really found you by accident, while I was looking on Yahoo for something else, Anyways I am here now and would just like to say thanks a lot for a incredible post and a all round enjoyable blog (I also love the theme/design), I don’t have time to go through it all at the moment but I have saved it and also added your RSS feeds, so when I have time I will be back to read a lot more, Please do keep up the excellent work.

  18. Welcome to your next beauty destination!

    Founded in 2014 by a female entrepreneur in Dubai with a strong vision that every person is unique and needs his beauty treat to fulfill his ultimate potential, an Art of Beauty Center has become a preferred style destination for both expats and residents in Dubai.
    An „Art of Beauty“ brand as first one in the UAE, that despite of the difference in cultural and linguistic barriers, as well as social norms of a new country, is offering an ultimate approach for a beauty care as an essential part of individual health care. It`s one of the selected salons, that offers a wide range of face, hair, and body treatments for all- ladies, gentlemen, and children.
    With a code of ethics, Art of Beauty eventually appeared to be to be a choice for personal care and beauty advice for many people with different background, age, nationality and workplace and interests. Over the first six months, the beauty center has shown its commitment to high professional standards and a delicate approach to individuality for everyone, who came here for an exceptional and delightful experience.
    Today, The Art of Beauty Center is a diverse range of professional`secrets and self-determination of every member of the team to perfection to create your phenomenal visual look and number one feeling.

  19. Pingback: Google

Comments are closed.