JOURNAL OF BACTERIOLOGY, July 1969, p. 116-124Copyright ( 1969 American Society for Microbiology

Vol. 99, No. IPrinted In U.S.A.

Synthesis of Bacterial FlagellaII. PBS1 Transduction of Flagella-specific Markers in Bacillus subtilis

GEOFFREY F. GRANT1 AND MELVIN I. SIMONDepartment of Biology, Revelle College, University of California, San Diego, La Jolla, California 92037

Received for publication 22 January 1969

The linkage relationship of mutants involved in the synthesis of flagella was de-termined by PBS1 transduction. Mutants that affect the structure of flagellin(hag) and temperature-sensitive mutants (flaTS) that produce flagella when grownat 37 C but not when grown at 46 C were examined. All of the mutants were found tobe linked to the hisAl marker. The flaTS mutants fell into three clusters. GroupA contained the majority of mutants which were loosely grouped around the haglocus. Group B mutants were segregated from the hag locus and appeared closelylinked to the phage adsorption site gene (gtaA), and group C was only looselylinked to hisAI and thus far contains only one mutant. A flagella locus (ifm) affect-ing both the degree of motility and level of flagellation was shown to map neargroup A. Mutants affecting motility (mot) were not linked to hisAI by PBS1 trans-duction. Several markers previously shown to link to hisAI were ordered withrespect to hisAI and the flagellar genes.

Previous work on the genetic control of flagel-lation in Bacillus subtilis (7) has defined theexistence of at least three classes of mutationanalogous to those found in Salmonella typhi-murium, hag, fla, and mot. The hag group involvesmodification of the structure of the flagellar fila-ment subunit protein. The wild-type W23 strain,for example, possesses immunologically distinctflagellin (hag-2) which differs from wild-type168 (hag-i) in both amino acid composition andpeptide sequence (S. Emerson, personal com-munication).The fla mutants phenotypically lack flagella

and are presumably defective in functions in-volved in the synthesis and assembly of the or-ganelle. They are readily isolated in B. subtilisbut are difficult to examine genetically. The prob-lem stems from the fact that both transductionwith SPIO and transformation establish linkagerelationships over only relatively short, well-defined intervals of the map, whereas transduc-tion with PBS1, which allows the transfer ofextensive fractions of the genome, is mediated bya flagella-specific virus which does not adsorb tofla recipient cells (5). To establish a system forboth genetic and biochemical study of flagellasynthesis, we used the known variants of thestructural gene (hag-i, hag-2, hag-3) and alsoisolated a number of temperature-sensitive mu-

' Present address: Salk Institute for Biological Studies, LaJolla, Calif. 92037.

tants (flaTS). The flaTS mutants allow the ad-sorption of PBS1 and hence transduction at37 C, but they do not possess flagella at 46 C andcan, therefore, be scored for recombination.A preliminary report on the mapping of fla-

gella mutants in B. subtilis was presented at the68th Annual Meeting of the American Society forMicrobiology, Detroit, Mich., 5-10 May 1968.

MATERIALS AND METHODSMedia. Basal medium was a minimal salts medium

(2) supplemented with either 0.1% Casamino Acidsand 30 lsg of appropriate growth requirements per ml,or, when selective medium was required, 20 ,g of allamino acids and requirements per ml excepting theparticular growth factor used as a selective agent.

Soft motility agar was composed of basal mediumsupplemented with 0.4% agar and 0.8% gelatin; whenappropriate, sufficient flagella-specific antiserum wasadded to inhibit motility.

Antibodies and antigens. B. subtilis flagellar proteinwas purified and antisera were prepared as previouslydescribed (6).

Nomenclature. To assign consistent designations toflagellar mutations in this study, we have adhered tothe conventions proposed by Demerec et al. (3). Sincewe assume, on the basis of both our data and the datapresented by Frankel and Joys (5) that the flagellarantigens represent alternate alleles of a single hag gene,the wild-type 168 antigen has been designated hag-1; the W23 antigen, hag-2; and the straight fila-ment mutation reported by Martinez et al. (8), hag-3.Genetic analysis on B. subtilis is not refined enough,at this stage, to completely rule out the possibilityof multiple hag cistrons.

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Strains. Tables 1 and 2 show the properties and in a number of ways. The mutants described in thisorigin of strains of B. subtilis used and prepared in paper were isolated following treatment withthis investigation. All parent strains were selected for N-methyl-N'-nitro-N-nitrosoguanidine at 100 &g/mlrapid motility by passage through motility tubes. (approximately 50% survival) according to the proce-The selection offlaTS mutants may be accomplished dure of Adelberg et al. (1). They were selected by

TABLE 1. Strains of B. subtilis

GenotypeStrain Origin Derivation

Auxotrophic markers hag Other markers

W23MH-1BD71BR19Rog 1

Rog 3

BR19 (hag-2)

BR13BR13 (hag-2)

BR85SB-3FY'A'JH1057G-2

SO-49G-5

G-10

SC-3 and SC4

G-22

flaTS -I{o -10 +flaTS -32to -47+

flaTS -18 to -23

flaTS -51

G-25

G31

G26

trp-2 lyshisAl, ura, argC4hisAl, trp-2

hisAl, trp-2

hisAl, trp-2

ura-1, trp-2ura-1, trp-2

argC4, trp-2hisAl, trp-2, cysBtrp-2trp-2 met4hisAl, ura, argC4

trp-2hisAl, argC4

argC4

trp-2

hisAl, ura

trp-2, lys

trp-2, ura

hisAl, ura, argC4

hisAl

hisAl

hisAl, ura

2

1

1

1

1

1

2

12

11

1

1

2

1

2

2

3

3

1

1

1

2

1

2

rou-l

rou-lspoCI

spoCl

rou-l

rou-lrou-l

rou-l

gtaA rou-luvr-l

motgtaA

gtaA

gtaA, uvr-1,ifm-l

gtaA, uvr-lifm-l

uvr-1, ifm-l

Wild type

Marburg wild typecured for sporula-tion marker withacridine orange

BR19 transformedwith Rog 1 DNA

BR19 transformedwith W23 DNA

BR13 transformedwith W23 DNA

BD71 transformedwith W23 DNA

G2 transformed withexcess FY'A' DNAselection of gtaAby congressioneliminating ura

G-5 transduced withPBS1 lysate ofMH-1

Nonmotile mutantpossessing straightflagella; antigen-ically hag-i

BD71 transformedwith SC4 DNA

Nitrosoguanidinemutagenesis ofMH-1

Nitrosoguanidinemutagenesis ofBR13

Nitrosoguanidinemutagenesis ofBD71

G5 transformed withexcess JH1057 DNA

G25 transformedwith FY'A' DNA

G2 transformed withexcess JH1057 DNA

SpizizenSueokaDubnauReillyRogolsky

Rogolsky

Reilly

ReillyNesterYoungHoch

Joys (7)

Martinez

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GRANT AND SIMON

cycling cells through high (46 C) and low (37 C)temperatures and transferring the fraction of theculture which agglutinated at 37 C but not at 46 Cwith flagella-specific antibodies. The process wasrepeated four or five times, and the cells were platedin soft motility agar for single colonies at 46 C.Nonmotile clones were picked, restreaked, and testedfor their ability to produce flagella at both tempera-tures. The mutants used for mapping produce few or

TABLE 2. Relative position of hag replacement locuson B. subtilis chromosomea

SelectedRecipient strain auxotrophic

markers

BR-27........BR-5.........BR-62........BR-77........SB-8.........BR-19........BR-85........BR-51...BR-13........BR-123.......BR-44........BR-84........BR-76........BR-76........BR-50......

ade-4ade-lade-5thr-1cysBhisAlargC4metA7ura-largOIleu-6phe-3lys-3trp-2met-6

Migrationthru minimalagar contain-ing antibody

+(+)+

Binding of1251-hag-2antibodyb

< 1,000

TRANSDUCTION OF FLAGELLAR MARKERS

Stock virus was prepared by infection of an early logculture of B. licheniformis in Penassay Broth (Difco).After lysis, the phage were purified and concentratedby differential centrifugation. The preparation oftransducing lysates and the transduction were carriedout according to the procedures of Reilly and Spizizen(personal communication). Donor strains were inocu-lated into Penassay Broth from overnight TryptoseBlood Agar Base (TBAB; Difco) plates and weregrown to an optical density of approximately 150Klett units; they were then infected with stock PBS1at a multiplicity of 5. The infected lysate was incubatedwith shaking for 3 to 4 hr. The culture was thenallowed to undergo autolysis by removing it from theshaker and incubating it overnight at 37 C. The lysatewas treated with deoxyribonuclease (1 jug/ml) andcentrifuged at 6,000 X g for 10 min. The supernatantfluid was sterilized by passage through a 0.45-Mmsterile membrane filter.

Recipient strains were streaked on TBAB platesand grown overnight; they were then heavily inocu-lated into Penassay Broth and grown for 5 hr untilmaximal motility was obtained. The recipient cultureand transducing lysate were mixed in equal volumesand diluted 1: 2 into fresh Penassay Broth followed byincubation for 20 min with shaking. The infected cellswere washed twice in minimal salts by centrifugation,and were plated on selective media in the presence ofsterile PBSI antiserum. Recombinant clones werepicked and restreaked on selective agar. The observedrecombination frequency was approximately 10-5/bac-terium. Nutritional and phage (t25)-resistancemarkers (gtaA) were scored by replica-plating by useof pads of velveteen; flagella markers were scored by

replica-plating by use of an inverted flower holder(frog) which was placed onto soft motility agar plateswith or without flagella antiserum and incubated at37 or 46 C, or at both temperatures. Figure 2 showshow flagella markers were identified.

Transformation. Transforming deoxyribonucleicacid (]DNA) was isolated by the procedure of Massieand Zimm (9) with the use of lysozyme and Pronase.Transformation was carried out according to themethod of Anagnostopoulos and Spizizen (2). Flagellaantigenic types were selected by inoculating trans-formed populations into motility tubes containingantisera specific for the recipient flagella and pickinga recombinant that passed rapidly through the tube.

RESULTS

Linkage of hag locus to hisAl. The generallocation of the hag gene on the B. subtilis chro-mosome was established by the use of strainswhich have antigenically non-cross-reacting fla-gella (hag-i and hag-2). A large number ofauxotrophic strains were used, all of whichrequired indole (trp-2) and one other marker.The second marker was chosen so that linkagewith various parts of the chromosome could bedemonstrated (Table 2). Transducing lysateswere grown on strains with hag-2 flagella andwere used to infect the hag-i auxotrophs. Link-age of the hag locus was demonstrated (i) bygrowing recombinants in selective media andmeasuring hag-2 flagellar antigen with radio-

2

4

370 C

hog-I Ab

I hog-I flogello2 hoq-2 flogello3 hog- I flI TS4 f/la

3460 C

hao-2 Ab

FIG. 2. Demonstration of the technique used to score flaTS and hag recombinants. The flaTS recombinantswere scored by incubation ofplates at 37 and 46 C (upper petri plates), and the hag recombinants were identifiedby use ofagar containing flagellar specific antibodies (lowerpetri plates).

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GRANT AND SIMON

active antibodies, and (ii) by inoculating thetransduced population into motility tubes con-taining hag-i flagellar antibody but lacking aspecific nutrient. Under these conditions, onlyhag-2 prototrophic recombinants could migratethrough the agar. The hag locus was found to belinked only to the cysB and hisAl markers(Table 2). Linkage was observed when the phagewere grown on derivatives of 168 strains carryingthe hag-2 locus. When the phage were prepared

directly on the W23 strain and used to infect168 derivatives, no linkage was observed.

Relative map position of the hag locus. ThehisAl locus has been shown to be linked to anumber of mutations. Dubnau et al. (4) mappedhisAI between cysB and argC4, and found 20%linkage to each of these markers. Other markersthat have been placed in this region of the chro-mosome are the phage-resistance markers gtaA,B, and C (12); a sporulation marker, spoCI

TABLE 3. Linkage relationships of markers to hisAl

Recipient Donor lysate marker Recombinant classes duction

BR19 BR13 (hag-2) his+ his+ hag-2, 350/686 51SB3 BR13 (hag-2) his+ his+ hag-2, 128/260 49

his+ cysB+, 112/564 20his+ cysB+ hag-2, 14/260 5.4

BR85 BR13 (hag-2) arg+ arg+ his+, 0/120BD71 BR13 (hag-2) his+ his+ hag-2, 96/184 52

his+ arg+, 0/120arg+ arg+ his+, 0/120

BD71 FY'A' his+ his+ rou-J, 403/673 60his+ rou-i gtaA, 236/673 35his+ rou+ gtaA, 340/673 50.5

BR-19 (hag-2) FY'A' his+ his+ hag-i, 61/90 68his+ hag-i gtaA, 48/90 53.5his+ hag-2 gtaA, 2/90 2

Rog 3 BR13 (hag-2) his+ his+ spoCI hag-2, 96/192 50his+ spo+ hag-2, 28/192 14.5his+ spo+ hag-i, 8/192 4

BD71 Rog-1 his+ his+ spoCI, 24/150 16his+ arg+, 0/150

1H1057 G-10 his+ his+ uvr+, 108/140 77his+ uvr+ hag-2, 81/140 58his+ uvr+ hag-2 gtaA, 65/140 46.5

rou-l

40

hisAifm

uvr-I hog gztaA

A BfloTS gene

spoCI

Cclusters

gtaC orgC4. o1

9031

3742

5384

FIG. 3. PBSI transduction map of the hisAl linkage group in Bacillus subtilis. Distances were determinedfromthe average of all experiments carried out during the course of this work (Table 7). Although the relative order ofifm and hag have been established (Table 4), the relative position of the flaTS markers that fall in this region hasnot as yet been completely determined.

r

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(10); a locus controlling radiation resistance,uvr-1; and a morphological marker, rou-1. Theresults of crosses designed to establish the rela-tive map position of these markers with respectto hisAl and hag are shown in Table 3 and aresummarized in Fig. 3 and Table 7.

Cotransduction of flagella-related markers.Mutations in the ifm locus change the relativequantity of flagella per cell as well as the motilityof the cells (see Materials and Methods); the

function that is affected in these mutants is notknown, and crosses were designed to determine(i) whether ifm clearly segregates from hag and(ii) its relative position on the map.

In the first cross, a hisAl, uvr-1, hag-2, ifm-1strain was used as recipient, and a hag-i, ifm+strain was used as donor. When recombinantswere replicated onto 0.4% agar, the ifm recom-binants could be clearly distinguished (Fig. 1).The data show that ifm segregates from hag-i;

TABLE 4. Segregation of ifm, gta, and hag among his+ transductantsa

+ + + hag-i +(1) Donor MHI, genotype hisAl uvr-i ifm-l hag-2 gtaA

Recipient G25his uvr ifm hag gta No. in class

1 0 0 0 0 441 1 0 0 0 131 1 1 0 0 101 1 1 1 0 251 1 1 1 1 481 0 0 0 1 2

No. with donor allele 142 96 83 73 50 142

+ + + hag-3 +(2) Donor SC4 genotype hisAl uvr-i ifm-i hag-i gtaA

Recipient G31his uvr ifm hag gSa No. in class

1 0 0 0 0 581 1 0 0 0 3

1 0 0 81 1 NDb 1 0 161 1 NDb 1 1 501 0 0 0 1 11 0 NDb 1 1 21 1 0 0 1 11 1 1 0 1 1

No. with donor allele 140 79 9b 68 55 140

+ + + hag-i gStaA(3) Donor FY'A' genotype hisAI urr-i irm-i hag-2 +

Recipient G26his uvr ifm hag g8aA No. in class

1 0 0 0 0 381 1 0 0 0 81 1 1 0 0 61 1 1 1 0 161 1 1 1 1 681 0 0 0 1 11 1 0 0 1 21 1 1 0 1 2

No. with donor allele 141 102 92 84 73 141

a The frequencies of all observed recombinant classes are shown. The donor allele is represented

determined. The total thereforeby a 1 and the recipient by a 0.

"The ifm character of the recombinants that were hag-3 was notrepresents the recombinants that were ifm+, hag-l.

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of the his+ recombinants tested, 10 of 140 wereifm+, hag-2 (Table 4). In a second cross, thedonor strain was hag-3, ifm+, and the recipientwas hisAl, uvr-1, hag-i, gtaA, and ifm-i. Again,ifm was found to segregate from hag, and 9 of140 recombinants were hag-i, ifm+. In the thirdcross, the same pattern of segregation was found.These data are consistent with the order uvr-ifm-hag-gta.

Table 5 shows the results of crosses performedto determine the relationship of theflaTS markersto the hag locus. In all, 26 temperature-sensitivemutants were tested and approximately 150 his+recombinants were picked in each cross. Sinceeach cross required lysates grown on the flaTSstrains, a fair amount of variation in the fre-quency of recombination for the hag region wasexpected. Table 5 includes the extremes in thevariation obtained. In spite of these differences,the mutants clearly fall into three distinct groups.Group A includes 21 mutants, all of which mapnear hag. The ratio of the frequency of recombin-ants for flaTS to that for hag-i is in the rangeof 1.1 to 0.92, and the ratio of flaTS to gtaA is1.6 to 1.2. Group B contains three mutants; theratio of flaTS to hag-i is 0.86 to 0.77, and theratio of flaTS to gtaA is 1.0. There is thus faronly one mutant that maps in Group C. It isclearly separable from the hag and the gtaA loci.To check further the position of the group B

TABLE 5. Transduction offlaTS mutants

flaTSdonorlysate

9404328

2210377

204613

51

Percentage of hisAl recombinantsa

hag-i IflaTSI gtaA+

7268586566706574616855657058

8075566266656668627258565422

5557405152424048425047575544

hag-l,

fla0

1

866666442171939

kag-2, flaTSflaTS to hag

5

96460

715

860

72

1.111.100.970.961.000.931.020.921.021.061.050.860.770.38

Ratio

1.451.321.401.281.261.551.621.541.481.451.250.990.990.50

a The recipient in all these experiments was G-5(hisAI, hag-2, gtaA). The donor lysates were pre-pared on the appropriate flaTS strain. hisAI+recombinants were picked and tested for the othermarkers. The results are presented as the per-centage of hisAI+ recombinants that carry a givenmarker.

mutants, flaTS-I and flaTS-7 were put into astrain carrying the gtaA marker and then crossedinto BD-71. In this cross, flaTS-I was found tobe closely linked to gtaA; the ratio of recombin-ants for flaTS to those for gtaA was 1.05, andthe ratio for flaTS-7 to gtaA was 1.2.

Table 5 also shows that in all the crossesrecombinants were obtained that were eitherhag-i, fla+ or hag-2, flaTS, suggesting that allthe flaTS markers mapped can segregate fromthe hag locus. However, the data obtained thusfar do not allow us to assign the precise positionsof all of theflaTS markers relative to one anotherand to the hag locus.We have assumed thus far that there is no

phase variation in B. subtilis. Our results couldbe complicated if these strains carried two sepa-rable hag genes and only one was phenotypicallyexpressed. To test this possibility, hag-3 mutantswere used. The hag-3 gene is derived from hag-iby mutation and has been shown to differ inonly a single peptide (8). Strains carrying hag-3are nonmotile and have flagella that are anti-genically identical to the hag-i product but lackthe normal long-period helix. In the crossesshown in Table 6, recombinants that were non-motile were picked and tested for antigenicspecificity. None of the nonmotile recombinantshad hag-2 antigen, and all of the nonmotilerecombinants had flagella. Furthermore, norecombinants of the hag-i type were found. Infurther crosses, over 1,000 recombinants havebeen picked and tested, and thus far only asingle hag-i recombinant has been found. There-fore, these data suggest that the strains do notcarry cryptic alternate hag genes that are linkedto hisAI.We have also found that the motility-negative

mutation (mot) reported by Joys and Frankel(7) does not cotransduce with hisAI.

DISCUSSIONGenetic crosses done by use of phage PBS1

established the linkage of the hag locus to hisAI.The relationship of flagella markers to othermarkers cotransferred with hisAI is shown inFig. 3 and Table 7.

It was not found possible to demonstratelinkage of hisAI to argC4, as was reported byDubnau et al. (4); in fact, the spoCI marker ofRogolsky (10) was demonstrated to be lesstightly linked to hisAI (16%) than the reportedlevel of cotransfer of the argC4 marker (24%).None of the hisAI linked markers could beshown to cotransfer with argC4. However, F.E. Young (J. Bacteriol., in press) and Grant andSimon (unpublished data) have shown that insome specific strains hisAI and argC4 may be

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TABLE 6. Test for a cryptic hag gene

Recipient Donor Motility Recombinant classesphenotypeReobnnclss

G5 SC-3 _ his+, hag-3, 94/192hisAl, hag-2, gtaA hag-3 _ his+, hag-3, gtaA, 42/192

+ his+, hag-2, 56/192

G5 SC-4hisAl, hag-2, gtaA hag-3 _ his+, hag-3, 97/200

_ his+, hag-3, gtaA, 35/200+ his+, hag-2, 68/200

G22 G10hisAI, hag-3 hag-2, gtaA + his+, hag-2, gtaA, 79/140

+ his+, hag-2, 11/140his+, hag-3, 50/140

TABLE 7. Summary of cotransductioni frequencies ofmarkers with hisA1a

Total fraction of Percentage ApproximateMarker his+ recombinants of cotrans- linkage

for linked markers fer (Y) (100 - Y)

rou-l 403/673 60 40uvr-l 775/1,120 69 31ifm 444/700 63 37hag 899/1,540 58 42gtaA 863/1,820 47 53spoCi 65/412 16 84

a The relative order of these markers has beenestablished and was consistently found in all ofthe transduction experiments. The degree of link-age summarizes our data. The cysB marker wasfound to map to the left of rou-i (Table 3).

cotransferred by PBS1 transduction. Young hasalso shown transformation linkage between thephage-resistance markers gtaA and gtaC whichdo not normally cotransfer in PBS1 transduction.This behavior suggests the presence of a chromo-somal abnormality or an unstable chromosomalelement that can be inserted in this region, e.g.,a defective lysogenic phage or an unstable epi-some. However, more experimentation is obvi-ously necessary to clarify this problem.

All of the hag and flaTS mutants that we havetested thus far are linked to hisAl by cotrans-duction. Although the data do not allow us toestablish unequivocally the position of all ofthese markers, it is clear that most of them clusteraround the hag locus. Some mutants (flaTS-Iand -3) appear to be more closely associatedwith the gta locus and segregate from hag. Onemutant (flaTS-51) is clearly separated from theothers.The lack of more markers in this region and

the absence of a reliable complementation systemin B. subtilis has prevented us from establishingdiscrete functional classes for the flaTS mutants.The data available, however, suggest that mostof them do not directly affect the structural genefor flagellin. This is certainly clear for the groupB and C mutants, which can be readily separatedfrom the hag locus. However, even the group Amutants, in almost all of the crosses, were foundto segregate from hag and give hag-2, flaTS orhag-i, fla+ recombinants.

Furthermore, tests of the flagellin proteins ofthese mutants also indicate that they do notdiffer from the wild-type protein (Dimmitt andSimon, unpublished data). These data suggestthat the flaTS mutants are defective in ancillaryfunctions that are required for the formation ofbacterial flagella. Further work is being directedtoward elucidating these functions, and towarddetermining the gene order in the group Aregion.

ACKNOWLEDGMENTS

We thank J. Spizizen, J. Hoch, and especially B. Reilly andF. E. Young, of Scripps Clinic and Research Foundation for pro-viding, not only many of the strains used, but also many ideasand criticisms of the work.

This work was supported by grant GB-6980 from the NationalScience Foundation.

LITERATURE CITED

1. Adelberg, E. A., M. Mandel, and G. C. C. Chen. 1965.Optimal conditions for mutagenesis by N-Methyl-N'-N'Nitrosoguanidine in Escherichia coll. Biochem. Biophys.Res. Commun. 18:788-795.

2. Anagnostopoulos, C., and J. Spizizen. 1961. Requirements fortransformation in Bacillus subtills. J. Bacteriol. 81:741-746.

3. Demerec, M., E. A. Adelberg, A. J. Clark, and P. E. Hart-man. 1966. A proposal for a uniform nomenclature in bac-terial genetics. Genetics 51:61-76.

4. Dubnau, D., C. Goldthwaite, I. Smith, and J. Marmur.1967. Genetic mapping in Bacillus subtilis. J. Mol. Biol.27:163-188.

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5. Frankel, R. W., and T. M. Joys. 1966. Adsorption specificityof bacteriophage PBSI. J. Bacteriol. 92:388-389.

6. Grant, G. F., and M. Simon. 1968. Use of radioactive anti-bodies for characterizing antigens and application to thestudy of flagella synthesis. J. Bacteriol. 95:81-86.

7. Joys, T. M. 1965. Correlation between susceptibility to bac-teriophage PBSI and motility in Bacillus subtills. J. Bac-teriol. 90:1575-1577.

8. Martinez, R. J., A. T. Ichiki, N. P. Lundh, and S. R. Tronick.1968. A single amino acid substitution responsible foraltered fagellar morphology. J. Mol. Biol. 34:559-564.

N[D SIMON J. BACTERIOL.

9. Massie, H. R., and B. H. Zimm. 1965. Molecular weight ofthe DNA in the chromosomes of E. coil and B. subtilts.Proc. Nat. Acad. Sci. U.S.A. 54:1636-1641.

10. Rogolsky, M., and R. Slepecky. 1968. The response of sporo-genesis in B. subtilis to acriflavine. Can. J. Microbiol.14:61-70.

11. Takahashi, I. 1963. Transducing phages for Bacillus subtilis.J. Gen. Microbiol. 31:211-217.

12. Young, F. E. 1967. Requirement of glucosylated teichoicacid for adsorption of phage in Bacillus subtilis 168. Proc.Nat. Acad. Sci. U.S.A. 58:2377-2384.

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